Patent Application
20140051843
1. Field of the Invention
The present invention relates to the fields of biotechnology and molecular biology. In particular, the present invention relates to the construction and use of nucleic acid molecules comprising sequences encoding polypeptides having a detectable activity. In a particular embodiment, the present invention relates to nucleic acid molecules encoding all or a portion of a polypeptide having β-lactamase activity.
2. Related Art
Reporter genes have found widespread use in the practice of biotechnology (see, for example, Molecular Cloning, second edition, editor J. Sambrook et al., Cold Spring Harbor Laboratory Press (1989)). One application of reporter genes is for the measurement of the promoter activity of a nucleotide sequence. This permits the identification of nucleotide sequences that promote the expression of particular sequences of interest in a host cell. This is particularly useful in identifying promoters that function in specific cell types (e.g., tissue-specific promoters).
To determine the promoter activity of a nucleic acid sequence, a nucleic acid molecule is constructed in which a nucleic acid sequence encoding a polypeptide having a detectable activity (i.e., a reporter gene) is operably linked to a nucleic acid sequence to be tested as a promoter. The nucleic acid molecule is then introduced in a host cell and the host cells are assayed for the presence and/or amount of the detectable activity. The amount of activity detected is indicative of the relative strength of the tested sequence as a promoter. Typically, reporter genes are selected for the ease with which their activity can be determined. Another consideration is whether the host cells contain an activity that can interfere with the assay.
Another use of reporter genes is in the construction of fusion proteins. Typically, a nucleic acid molecule is constructed such that a nucleic acid sequence encoding a polypeptide having a detectable activity (i.e., a reporter gene) is placed adjacent to a nucleic acid sequence encoding a polypeptide of interest. As is well known in the art, the two sequences may be placed such that the coding sequences of the two polypeptides are in the same reading frame. This results in the expression of a fusion polypeptide containing both the polypeptide encoded by the reporter gene and the polypeptide of interest. Cells containing the fusion polypeptide can be detected by assaying for the detectable activity.
Nucleic acid sequences encoding a wide variety of polypeptides have been used as reporter genes. Some of the polypeptides encoded include, but are not limited to, enzymes (e.g., chloramphenicol acetyl transferase, alkaline phosphatase, luciferase, β-galactosidase, β-glucuronidase, etc.) and fluorescent proteins (e.g., green fluorescent protein, yellow fluorescent protein, red fluorescent protein, cyan fluorescent protein, etc.). The β-lactamase gene has been used as a reporter and detection system for protein expression in mammalian cells (see, for example, Whitney et al. (1998) Nat. Biotechnol. 16:1329-33; and Zlokarnik, et al. (1998) Science 279:84-88).
After expression of a polypeptide in a host cell (e.g., a fusion polypeptide), it is typically necessary to separate the desired polypeptide from the other components of the host cell. Affinity chromatography is often the preferred method for polypeptide purification and can often be used to purify polypeptides from complex mixtures with high yield. Affinity chromatography is based on the ability of polypeptides to bind non-covalently but specifically to an immobilized ligand for the desired polypeptide. A number of peptides and polypeptides have been used for affinity chromatography, for example, the six histidine peptide, various epitopes (e.g., the V5 epitope), glutathione S-transferase (GST), the maltose-binding protein, etc. Peptides having an affinity for a biarsenical compound have been used for affinity purification (see, for example, U.S. Pat. Nos. 5,932,474, 6,008,378, 6,054,271, and 6,451,569 and published international patent application WO 01/53325A2).
The present invention relates to nucleic acid sequences encoding polypeptides having a detectable activity and nucleic acid molecules comprising such sequences. Detectable activity may be any characteristic that can be detected, for example, enzymatic activity, fluorescence, binding activity, and the like. In some embodiments, detectable activity may be a β-lactamase activity. In particular embodiments, a detectable activity may be an activity that can alter the fluorescence (e.g., increase florescence yield, decrease fluorescence yield, change the emission wavelength, etc.) of a fluorescent substrate with which the polypeptide interacts. In some embodiments, a detectable activity may involve binding of the polypeptide to specific molecules (e.g., molecules comprising one or more arsenic atoms). Nucleic acid molecules of the invention may also comprise one or more (e.g., one, two, three, four, five, etc.) recombination sites (e.g., one or more att sites, one or more lox sites, etc.) and/or one or more (e.g., one, two, three, four, five, etc.) topoisomerase recognition sites (e.g., one or more recognition sites for a type IA topoisomerase, a type IB topoisomerase, a type II topoisomerase, etc.). Such nucleic acid molecules also include nucleic acid molecules that have undergone cleavage (e.g., cleavage of one strand of the nucleic acid molecules) with a topoisomerase (e.g., a site specific topoisomerase). Further, one or more topoisomerase molecules may be bound (e.g., covalently bound) to each nucleic acid molecule which is cleaved. Optionally, nucleic acid molecules comprising a sequence encoding a polypeptide having a detectable activity may comprise one or more recombination sites and/or one or more topoisomerases. The invention also relates to vectors comprising one or more nucleic acid molecules of the invention as well as variants and derivatives of these vectors.
In particular embodiments, the invention relates to combining or joining at least a first nucleic acid molecule which comprises at least a first nucleic acid sequence encoding a polypeptide having a detectable activity (e.g., a β-lactamase) and also comprises at least one topoisomerase site and/or topoisomerase and at least a second nucleic acid molecule that comprises a nucleic acid sequence to be assayed for promoter activity (e.g., a nucleic acid sequence which potentially has one or more activities associated with promoters). Optionally, the first nucleic acid molecule comprises one or more recombination sites. When a first nucleic acid molecule comprises two or more recombination sites, such sites may be engineered recombination sites and may not recombine or substantially recombine with each other. Optionally, a second nucleic acid molecule may comprise one or more topoisomerase recognition sites and/or one or more topoisomerases and/or one or more recombination sites. When a second nucleic acid molecule comprises two or more recombination sites, such sites may be engineered recombination sites and may not recombine with each other.
Upon joining the at least first and second molecules, the sequence encoding a polypeptide having a detectable activity may be operably-linked to the sequence to be assayed for promoter activity. These nucleic acid molecules may be linear or closed circular (e.g., relaxed, supercoiled, etc.). Such recombination sites, topoisomerase recognition sites and topoisomerases can be located at any position on any number of nucleic acid molecules of the invention, including at or near the termini of the nucleic acid molecules and/or within the nucleic acid molecules. Moreover, any combination of the same or different recombination sites, topoisomerase recognition sites and/or topoisomerases may be used in accordance with the invention.
The invention also relates to nucleic acid molecules comprising nucleic acid sequences encoding polypeptides having a detectable activity and also comprising one or more recombination sites. Optionally, such nucleic acid molecules may comprise two recombination sites that do not recombine with each other. Such recombination sites may be located anywhere in the nucleic acid molecule and may be located such that at least one of the recombination sites is adjacent to the sequence encoding a polypeptide having a detectable activity. Optionally, a recombination site may have a sequence that encodes one or more amino acids in one or more reading frames. In some embodiments, a recombination site having a sequence encoding one or more amino acids in one or more reading frames may be located adjacent to the sequence encoding a polypeptide having a detectable activity. In such embodiments, amino acids encoded by the recombination site may be in the same reading frame as the polypeptide having a detectable activity. Such embodiments may produce a fusion protein comprising the polypeptide having a detectable activity and a peptide having one or more amino acids encoded by the sequence of the recombination site. In some embodiments, the peptide having one or more amino acids encoded by the sequence of the recombination site may comprise all of the amino acids encoded by the recombination site.
In some aspects, the present invention provides one or more methods for making nucleic acid molecules. Such methods may entail: (a) providing a first nucleic acid molecule comprising a first nucleic acid sequence encoding a polypeptide having a detectable activity and at least a first recombination site; (b) providing a second nucleic acid molecule comprising a second nucleic acid sequence to be assayed as a promoter and at least a second recombination site; and (c) forming a mixture in vitro between said first and second nucleic acid molecules and at least one recombination protein, under conditions sufficient to cause recombination in vitro between said first and second recombination sites, thereby producing a third nucleic acid molecule in which said first and second nucleic acid sequences are operably linked. Methods of the invention may further comprise (d) contacting one or more hosts or host cells with said mixture; and (e) selecting for a host or host cell comprising said third nucleic acid molecule, and selecting against a host or host cell comprising said first nucleic acid molecule and against a host or host cell comprising said second nucleic acid molecule. In particular embodiments, the second nucleic acid molecule above may be a member of a population of nucleic acid molecules which differ in sequence. Thus, the invention include methods for identifying nucleic acid molecules present in a mixed population which have one or more activities of associated with a promoter.
In another aspect, methods of making nucleic acid molecules of the invention may entail: (a) providing a first nucleic acid molecule comprising a first nucleic acid sequence encoding a polypeptide having a detectable activity and at least a first recombination site; (b) providing a second nucleic acid molecule comprising a nucleic acid sequence encoding a polypeptide of interest and at least a second recombination site; and (c) forming a mixture in vitro between said first and second nucleic acid molecules and at least one recombination protein, under conditions sufficient to cause recombination in vitro between said first and second recombination sites, thereby producing a third nucleic acid molecule comprising a third nucleic acid sequence that encodes all or a portion of the polypeptide having a detectable activity and all or a portion of the polypeptide of interest in the same reading frame and comprising a third recombination site that is the product of the recombination of the first and second recombination sites. In methods of this type, in the third nucleic acid molecule, the third recombination site may be located between the nucleic acid sequence encoding a polypeptide having a detectable activity and the nucleic acid sequence encoding a polypeptide of interest. In some embodiments, a fusion protein comprising all or a portion of the amino acid sequence of the polypeptide having a detectable activity, all or a portion of the amino acid sequence of the polypeptide interest and comprising at least one amino acid encoded by the third recombination site may be produced from the third nucleic acid molecule.
The invention includes, in part, nucleic acid molecules and compositions comprising nucleic acid molecules (e.g., reaction mixtures), wherein the nucleic acid molecules comprise (1) at least one (e.g., one, two, three, four, five, six, seven eight, etc.) recombination site and (2) at least one (e.g., one, two, three, four, five, six, seven eight, etc.) topoisomerase (e.g., a covalently linked topoisomerase) or at least one (e.g., one, two, three, four, five, six, seven eight, etc.) topoisomerase recognition site. In particular embodiments, the topoisomerases or topoisomerase recognition sites, as well as the recombination sites, of the nucleic acid molecules referred to above can be either internal or at or near one or both termini. For example, one or more (e.g., one, two, three, four, five, six, seven eight, etc.) of the at least one topoisomerase or the at least one topoisomerase recognition site, as well as one or more of the at least one recombination site, can be located at or near a 5′ terminus, at or near a 3′ terminus, at or near both 5′ termini, at or near both 3′ termini, at or near a 5′ terminus and a 3′ terminus, at or near a 5′ terminus and both 3′ termini, or at or near a 3′ terminus and both 5′ termini. The invention further provides methods for preparing and using nucleic acid molecules and compositions of the invention.
In a specific aspect, the invention provides nucleic acid molecules which comprise at least a first nucleic acid sequence encoding a polypeptide having a detectable activity to which topoisomerases of various types (e.g., a type IA topoisomerase, a type IB topoisomerase, a type II topoisomerase, etc.) are attached (e.g., covalently bound). In another specific aspect, the invention provides nucleic acid molecules which comprise at least a first nucleic acid sequence encoding a polypeptide having a detectable activity which contains two or more topoisomerase recognition sites which are recognized by one or more types of topoisomerases. The present invention also provides methods for preparing and using compositions comprising such nucleic acid molecules. In many embodiments, these nucleic acid molecules will further comprise one or more (e.g., one, two, three, four, five, six, seven, eight, etc.) recombination sites.
The invention further provides methods for joining two or more nucleic acid segments, at least one of which comprises at least a first nucleic acid sequence encoding a polypeptide having a detectable activity, wherein at least one of the nucleic acid segments contains at least one topoisomerase or topoisomerase recognition site and/or one or more recombination sites. Further, when nucleic acid segments used in methods of the invention contain more than one (e.g., two, three, four, five, six, seven eight, etc.) topoisomerase, either on the same or different nucleic acid segments, these topoisomerases may be of the same type or of different types. Similarly, when nucleic acid segments used in methods of the invention contain more than one topoisomerase recognition site, either on the same or different nucleic acid segments, these topoisomerase recognition sites may be recognized by topoisomerases of the same type or of different types. Additionally, when nucleic acid segments used in methods of the invention contain one or more recombination sites, these recombination sites may be able to recombine with one or more recombination sites on the same or different nucleic acid segments. Thus, the invention provides methods for joining nucleic acid segments using methods employing any one topoisomerase or topoisomerase recognition site. The invention provides further methods for joining nucleic acid segments using methods employing (1) any combination of topoisomerases or topoisomerase recognition sites and/or (2) any combination of recombination sites. The invention also provides nucleic acid molecules produced by the methods described above, as well as uses of these molecules and compositions comprising these molecules.
In general, the invention provides, in part, methods for joining one or more nucleic acid molecules or segments which comprises at least a first nucleic acid sequence encoding a polypeptide having a detectable activity with any number of nucleic acid segments (e.g., two, three, four, five, six, seven, eight, nine, ten, etc.) which contain different functional or structural elements. The invention thus provides, in part, methods for bringing together any number of nucleic acid segments (e.g., two, three, four, five, six, seven, eight, nine, ten, etc.) which confer different properties upon a nucleic acid molecule product. In many instances, methods of the invention will result in the formation of nucleic acid molecules wherein there is operable interaction between properties and/or elements of individual nucleic acid segments which are joined (e.g., operable interaction/linkage between an expression control sequence and at least a first nucleic acid sequence encoding a polypeptide having a detectable activity). Examples of (1) functional and structural elements and (2) properties which may be conferred upon product molecules include, but are not limited to, multiple cloning sites (e.g., nucleic acid regions which contain at least two restriction endonuclease cleavage sites), packaging signals (e.g., adenoviral packaging signals, alphaviral packaging signals, etc.), restriction endonuclease cleavage sites, open reading frames (e.g., intein coding sequence, affinity purification tag coding sequences, etc.), expression control sequences (e.g., promoters, operators, etc.), etc. Additional elements and properties which can be conferred by nucleic acid segments upon a product nucleic acid molecule are described elsewhere herein. The invention also provides nucleic acid molecules produced by the methods described above, as well as uses of these molecules and compositions comprising these molecules.
The invention further includes, in part, methods for joining two or more (e.g., 2, 3, 4, 5, 6, 7, 8, etc.) nucleic acid segments, wherein at least one (e.g., 1, 2, 3, 4, 5, 6, 7, 8, etc.) of the nucleic acid segments comprises at least a first nucleic acid sequence encoding a polypeptide having a detectable activity and comprises one or more (e.g., 1, 2, 3, 4, 5, 6, 7, 8, etc.) topoisomerases and/or one or more topoisomerase recognition sites and comprises one or more recombination sites. Thus, methods of the invention can be used to prepare joined or chimeric nucleic acid molecules by the joining of nucleic acid segments, wherein the product nucleic acid molecules comprise (1) one or more (e.g., 1, 2, 3, 4, 5, 6, 7, 8, etc.) topoisomerases and/or one or more (e.g., 1, 2, 3, 4, 5, 6, 7, 8, etc.) topoisomerase recognition sites and (2) one or more (e.g., 1, 2, 3, 4, 5, 6, 7, 8, etc.) recombination sites. The invention further provides nucleic acid molecules prepared by such methods, compositions comprising such nucleic acid molecules, and methods for using such nucleic acid molecules.
The invention also provides compositions comprising one or more nucleic acid segments and/or nucleic acid molecules described herein. Such compositions may comprise one or a number of other components selected from the group consisting of one or more other nucleic acid molecules (which may comprise recombination sites, topoisomerase recognition sites, topoisomerases, etc.), one or more nucleotides, one or more polymerases, one or more reverse transcriptases, one or more recombination proteins, one or more topoisomerases, one or more buffers and/or salts, one or more solid supports, one or more polyamines, one or more vectors, one or more restriction enzymes and the like. For example, compositions of the invention include; but are not limited to, mixtures (e.g., reaction mixtures) comprising a nucleic acid segment comprising a first nucleic acid sequence encoding a polypeptide having a detectable activity and at least one topoisomerase recognition site, and at least one topoisomerase which recognizes at least one of the at least one topoisomerase recognition sites of the nucleic acid segment. Compositions of the invention further include at least one nucleic acid segment comprising (1) a first nucleic acid sequence encoding a polypeptide having a detectable activity and at least one topoisomerase recognition site or at least one nucleic acid segment comprising a first nucleic acid sequence encoding a polypeptide having a detectable activity to which at least one topoisomerase is attached (e.g., covalently bound) and (2) one or more additional components. Examples of such additional components include, but are not limited to, topoisomerases; additional nucleic acid segments, which may or may not comprise one or more topoisomerases or topoisomerase recognition sites; buffers; salts; polyamines (e.g., spermine, spermidine, etc.); water; etc. Nucleic acid segments present in compositions of the invention may further comprise one or more recombination sites and/or one or more recombinase.
Often, nucleic acid molecules which have undergone cleavage with a topoisomerase (e.g., a site specific topoisomerase) will further have a topoisomerase molecule covalently bound to a phosphate group of the nucleic acid molecules. The invention further includes methods for preparing nucleic acid molecules described above and elsewhere herein, as well as recombinant methods for using such molecules.
In particular embodiments, nucleic acid molecules of the invention will be vectors. In additional embodiments, the invention includes host cells which contain nucleic acid molecules of the invention, as well as methods for making and using such host cells, for example, to produce expression products (e.g., proteins, polypeptides, antigens, antigenic determinants, epitopes, and the like, or fragments thereof).
In specific embodiments, nucleic acid molecules of the invention comprise two or more recombination sites with one or more (e.g., one, two, three, four, five, etc.) topoisomerase recognition site located between the recombination sites and comprise a first nucleic acid sequence encoding a polypeptide having a detectable activity that may be located outside the recombination sites.
In additional specific embodiments, circular nucleic acid molecules of the invention comprise two recombination sites with two topoisomerase recognition sites located between the two recombination sites and comprise a first nucleic acid sequence encoding a polypeptide having a detectable activity that may be located outside the recombination sites. Thus, if such molecules are linearized by cleavage between the topoisomerase recognition sites, the topoisomerase recognition sites in the resulting linear molecule will be located distal (i.e., closer to the two ends of the linear molecule) to the recombination sites and the sequence encoding a polypeptide having a detectable activity will be between the recombination sites. The invention thus provides linear nucleic acid molecules which contain at least a first nucleic acid sequence encoding a polypeptide having a detectable activity and one or more recombination sites and one or more topoisomerase recognition sites. In particular embodiments, the one or more topoisomerase recognition sites are located distal to the one or more recombination sites.
Recombination sites for use in the invention may be any recognition sequence on a nucleic acid molecule which participates in a recombination reaction catalyzed or facilitated by recombination proteins. In those embodiments of the present invention utilizing more than one recombination site, such recombination sites may be the same or different and may recombine with each other or may not recombine or not substantially recombine with each other. Recombination sites contemplated by the invention also include mutants, derivatives or variants of wild-type or naturally occurring recombination sites. Recombination site modifications include those that enhance recombination, such enhancement selected from the group consisting of substantially (i) favoring integrative recombination; (ii) favoring excisive recombination; (iii) relieving the requirement for host factors; (iv) increasing the efficiency of co-integrate or product formation; and (v) increasing the specificity of co-integrate or product formation. Particular modifications include those that enhance recombination specificity, remove one or more stop codons, and/or avoid hair-pin formation. Desired modifications can also be made to the recombination sites to include desired amino acid changes to the transcription or translation product (e.g., mRNA or protein) when translation or transcription occurs across the modified recombination site. Recombination sites that may be used in accordance with the invention include att sites, frt sites, dif sites, psi sites, cer sites, and lox sites or mutants, derivatives and variants thereof (or combinations thereof). Recombination sites contemplated by the invention also include portions of such recombination sites.
Topoisomerase recognition sites advantageously used in the nucleic acid molecules of this aspect of the invention will often be recognized and bound by a type I topoisomerase (such as type IA topoisomerases (including but not limited to E. coli topoisomerase I, E. coli topoisomerase III, eukaryotic topoisomerase II, archeal reverse gyrase, yeast topoisomerase III, Drosophila topoisomerase III, human topoisomerase III, Streptococcus pneumoniae topoisomerase III, and the traE protein of plasmid RP4) and type LB topoisomerases (including but not limited to eukaryotic nuclear type I topoisomerase and a poxvirus (such as that isolated from or produced by vaccinia virus, Shope fibroma virus, ORF virus, fowlpox virus, molluscum contagiosum virus and Amsacta moorei entomopoxvirus)), and type II topoisomerase (including, but not limited to, bacterial gyrase, bacterial DNA topoisomerase IV, eukaryotic DNA topoisomerase II (such as calf thymus type II topoisomerase), and T-even phage-encoded DNA topoisomerase).
Each starting nucleic acid molecule may comprise, in addition to at least a first nucleic acid sequence encoding a polypeptide having a detectable activity, a variety of sequences (or combinations thereof) including, but not limited to one or more recombination sites and/or one or more topoisomerase recognition sites and/or one or more topoisomerases, sequences suitable for use as primer sites (e.g., sequences which a primer such as a sequencing primer or amplification primer may hybridize to initiate nucleic acid synthesis, amplification or sequencing), transcription or translation signals or regulatory sequences such as promoters and/or operators, ribosomal binding sites, Kozak sequences, and start codons, transcription and/or translation termination signals such as stop codons (which may be optimally suppressed by one or more suppressor tRNA molecules), tRNAs (e.g., suppressor tRNAs), origins of replication, selectable markers, and genes or portions of genes which may be used to create protein fusion (e.g., N-terminal or carboxy terminal) such as GST, GUS, GFP, open reading frame (orf) sequences, and any other sequence of interest which may be desired or used in various molecular biology techniques including sequences for use in homologous recombination (e.g., gene targeting).
In another aspect of the invention, nucleic acid molecules of the invention include those which contain at least (1) one or more (e.g., one, two, three, four, five, six, seven, eight, nine, etc.) components of one or more of the vectors represented in
In one embodiment, a method of the invention is performed such that the first nucleic acid molecule (which may be ss or ds), as well as other nucleic acids used in methods of the invention, comprises at least a first nucleic acid sequence encoding a polypeptide having a detectable activity, and a second nucleic acid molecule (which may be ss or ds) is one of a plurality of nucleotide sequences, for example, a library, a combinatorial library of nucleotide sequences, or a variegated population of nucleotide sequences.
The present invention also relates to compositions prepared according to the methods of the invention, and to compositions useful for practicing the methods. Such compositions can include one or more reactants used in the methods of the invention and/or one or more ds recombinant nucleic acid molecules produced according to a method of the invention. Such compositions can include, for example, one or more nucleic acid molecules having at least one nucleic acid sequence encoding a polypeptide having a detectable activity, one or more nucleic acid molecules with one or more topoisomerase recognition sites; one or more topoisomerase-charge nucleic acid molecules; one or more nucleic acid molecules comprising one or more recombination sites; one or more primers useful for preparing a nucleic acid molecule containing a topoisomerase recognition site at one or both termini of one or both ends of an amplification product prepared using the primer; one or more topoisomerases; one or more substrate nucleic acid molecules, including, for example, nucleotide sequences encoding tags, markers, regulatory elements, or the like; one or more covalently linked ds recombinant nucleic acid molecules produced according to a method of the invention; one or more cells containing or useful for containing a nucleic acid molecule, primer, or recombinant nucleic acid molecule as disclosed herein; one or more polymerases for performing a primer extension or amplification reaction; one or more reaction buffers; and the like. In one embodiment, a composition of the invention comprises two or more different topoisomerase-charged nucleic acid molecules and/or two or more different recombination sites. The composition can further comprise at least one topoisomerase. A composition of the invention also can comprise a site specific topoisomerase and a covalently linked ds recombinant nucleic acid molecule, wherein the recombinant nucleic acid molecule contains at least one topoisomerase recognition site for the site specific topoisomerase in each strand, and wherein a topoisomerase recognition site in one strand is within about 100 nucleotides of a topoisomerase recognition site in the complementary strand, generally within about five, ten, twenty or thirty nucleotides.
Methods of the invention may comprise expressing a protein from one or more nucleic acid molecules of the invention. Protein expression steps, according to the invention, may comprise:
(a) obtaining a nucleic acid molecule to be expressed which comprises one or more expression signals; and
(b) expressing all or a portion of the nucleic acid molecule under control of said expression signal thereby producing a peptide or protein encoded by said molecule or portion thereof.
In this context, the expression signal may be said to be operably linked to the sequence to be expressed. The protein or peptide expressed is will often be expressed in a host cell (in vivo), although expression may be conducted in vitro using techniques well known in the art. Upon expression of the protein or peptide, the protein or peptide product may optionally be isolated or purified.
Compositions, methods and kits of the invention may be prepared and carried out using a phage-lambda site-specific recombination system. Further, such compositions, methods and kits may be prepared and carried out using the G
Recombination sites and topoisomerase recognition sites used in the methods of this aspect of the invention include, but are not limited to, those described elsewhere herein. In particular methods, nucleic acid molecules of the invention are joined with other nucleic acid molecules in the presence of at least one recombination protein, which may be but is not limited to Cre, Int, IHF, Xis, Fis, Hin, Gin, Cin, Tn3 resolvase, TndX, XerC, or XerD. In certain such embodiments, the recombination protein is Cre, Int, Xis, IHF or Fis.
The invention also provides kits comprising these isolated nucleic acid molecules of the invention, which may optionally comprise one or more additional components selected from the group consisting of one or more topoisomerases, one or more recombination proteins, one or more vectors, one or more polypeptides having polymerase activity, and one or more host cells.
Other embodiments of the invention will be apparent to one or ordinary skill in the art in light of what is known in the art, in light of the following drawings and description of the invention, and in light of the claims.
In the description that follows, a number of terms used in recombinant nucleic acid technology are utilized extensively. In order to provide a clear and more consistent understanding of the specification and claims, including the scope to be given such terms, the following definitions are provided.
As used herein, the following is the set of 20 naturally occurring amino acids commonly found in proteins and the one and three letter codes associated with each amino acid:
Gene: As used herein, the term “gene” refers to a nucleic acid that contains information necessary for expression of a polypeptide, protein, or untranslated RNA (e.g., rRNA, tRNA, anti-sense RNA). When the gene encodes a protein, it includes the promoter and the structural gene open reading frame sequence (ORF), as well as other sequences involved in expression of the protein. When the gene encodes an untranslated RNA, it includes the promoter and the nucleic acid that encodes the untranslated RNA.
Structural Gene: As used herein, the phrase “structural gene” refers to refers to a nucleic acid that is transcribed into messenger RNA that is then translated into a sequence of amino acids characteristic of a specific polypeptide.
Host: As used herein, the term “host” refers to any prokaryotic or eukaryotic (e.g., mammalian, insect, yeast, plant, avian, animal, etc.) organism that is a recipient of a replicable expression vector, cloning vector or any nucleic acid molecule. The nucleic acid molecule may contain, but is not limited to, a sequence of interest, a transcriptional regulatory sequence (such as a promoter, enhancer, repressor, and the like) and/or an origin of replication. As used herein, the terms “host,” “host cell,” “recombinant host” and “recombinant host cell” may be used interchangeably. For examples of such hosts, see Sambrook, et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y.
Transcriptional Regulatory Sequence: As used herein, the phrase “transcriptional regulatory sequence” refers to a functional stretch of nucleotides contained on a nucleic acid molecule, in any configuration or geometry, that act to regulate the transcription of (1) one or more structural genes (e.g., two, three, four, five, seven, ten, etc.) into messenger RNA or (2) one or more genes into untranslated RNA. Examples of transcriptional regulatory sequences include, but are not limited to, promoters, enhancers, repressors, operators (e.g., the tet operator), and the like.
Promoter: As used herein, a promoter is an example of a transcriptional regulatory sequence, and is specifically a nucleic acid generally described as the 5′-region of a gene located proximal to the start codon or nucleic acid that encodes untranslated RNA. The transcription of an adjacent nucleic acid segment is initiated at or near the promoter. A repressible promoter's rate of transcription decreases in response to a repressing agent. An inducible promoter's rate of transcription increases in response to an inducing agent. A constitutive promoter's rate of transcription is not specifically regulated, though it can vary under the influence of general metabolic conditions.
Target Nucleic Acid Molecule: As used herein, the phrase “target nucleic acid molecule” refers to a nucleic acid segment of interest, preferably nucleic acid that is to be acted upon using the compounds and methods of the present invention. Such target nucleic acid molecules may contain one or more (e.g., two, three, four, five, seven, ten, twelve, fifteen, twenty, thirty, fifty, etc.) genes or one or more portions of genes.
Insert Donor: As used herein, the phrase “Insert Donor” refers to one of the two parental nucleic acid molecules (e.g., RNA or DNA) of the present invention that carries an insert (see
Insert: As used herein, the term “insert” refers to a desired nucleic acid segment that is a part of a larger nucleic acid molecule. In many instances, the insert will be introduced into the larger nucleic acid molecule. For example, the nucleic acid segments labeled A in
Product: As used herein, the term “Product” refers to one the desired daughter molecules comprising the A and D sequences that is produced after the second recombination event during the recombinational cloning process (see
Byproduct: As used herein, the term “Byproduct” refers to a daughter molecule (a new clone produced after the second recombination event during the recombinational cloning process) lacking the segment that is desired to be cloned or subcloned.
Cointegrate: As used herein, the term “Cointegrate” refers to at least one recombination intermediate nucleic acid molecule of the present invention that contains both parental (starting) molecules. Cointegrates may be linear or circular. RNA and polypeptides may be expressed from cointegrates using an appropriate host cell strain, for example E. coli DB3.1 (particularly E. coli LIBRARY EFFICIENCY® DB3.1™ Competent Cells), and selecting for both selection markers found on the cointegrate molecule.
Recognition Sequence: As used herein, the phrase “recognition sequence” or “recognition site” refers to a particular sequence to which a protein, chemical compound, DNA, or RNA molecule (e.g., restriction endonuclease, a modification methylase, topoisomerases, or a recombinase) recognizes and binds. In some embodiments of the present invention, a recognition sequence may refer to a recombination site or topoisomerases site. For example, the recognition sequence for Cre recombinase is loxP which is a 34 base pair sequence comprising two 13 base pair inverted repeats (serving as the recombinase binding sites) flanking an 8 base pair core sequence (see FIG. 1 of Sauer, B., Current Opinion in Biotechnology 5:521-527 (1994)). Other examples of recognition sequences are the attB, attP, attL, and attR sequences, which are recognized by the recombinase enzyme λ Integrase. attB is an approximately 25 base pair sequence containing two 9 base pair core-type Int binding sites and a 7 base pair overlap region. attP is an approximately 240 base pair sequence containing core-type Int binding sites and arm-type Int binding sites as well as sites for auxiliary proteins integration host factor (IHF), FIS and excisionase (Xis) (see Landy, Current Opinion in Biotechnology 3:699-707 (1993)). Such sites may also be engineered according to the present invention to enhance production of products in the methods of the invention. For example, when such engineered sites lack the P1 or H1 domains to make the recombination reactions irreversible (e.g., attR or attP), such sites may be designated attR′ or attP′ to show that the domains of these sites have been modified in some way.
Recombination Proteins: As used herein, the phrase “recombination proteins” includes excisive or integrative proteins, enzymes, co-factors or associated proteins that are involved in recombination reactions involving one or more recombination sites (e.g., two, three, four, five, seven, ten, twelve, fifteen, twenty, thirty, fifty, etc.), which may be wild-type proteins (see Landy, Current Opinion in Biotechnology 3:699-707 (1993)), or mutants, derivatives (e.g., fusion proteins containing the recombination protein sequences or fragments thereof), fragments, and variants thereof. Examples of recombination proteins include Cre, Int, IHF, Xis, Flp, Fis, Hin, Gin, (DC31, Cin, Tn3 resolvase, TndX, XerC, XerD, TnpX, Hjc, SpCCE1, and ParA.
Recombinases: As used herein, the term “recombinases” is used to refer to the protein that catalyzes strand cleavage and re-ligation in a recombination reaction. Site-specific recombinases are proteins that are present in many organisms (e.g., viruses and bacteria) and have been characterized as having both endonuclease and ligase properties. These recombinases (along with associated proteins in some cases) recognize specific sequences of bases in a nucleic acid molecule and exchange the nucleic acid segments flanking those sequences. The recombinases and associated proteins are collectively referred to as “recombination proteins” (see, e.g., Landy, A., Current Opinion in Biotechnology 3:699-707 (1993)).
Numerous recombination systems from various organisms have been described. See, e.g., Hoess, et al., Nucleic Acids Research 14(6):2287 (1986); Abremski, et al., J. Biol. Chem. 261(1):391 (1986); Campbell, J. Bacteriol. 174(23):7495 (1992); Qian, et al., J. Biol. Chem. 267(11):7794 (1992); Araki, et al., J. Mol. Biol. 225(1):25 (1992); Maeser and Kahnmann, Mol. Gen. Genet. 230:170-176) (1991); Esposito, et al., Nucl. Acids Res. 25(18):3605 (1997). Many of these belong to the integrase family of recombinases (Argos, et al., EMBO J. 5:433-440 (1986); Voziyanov, et al., Nucl. Acids Res. 27:930 (1999)). Perhaps the best studied of these are the Integrase/att system from bacteriophage λ (Landy, A. Current Opinions in Genetics and Devel. 3:699-707 (1993)), the Cre/loxP system from bacteriophage P1 (Hoess and Abremski (1990) In Nucleic Acids and Molecular Biology, vol. 4. Eds.: Eckstein and Lilley, Berlin-Heidelberg: Springer-Verlag; pp. 90-109), and the FLP/FRT system from the Saccharomyces cerevisiae 2μ circle plasmid (Broach, et al., Cell 29:227-234 (1982)).
Recombination Site: A used herein, the phrase “recombination site” refers to a recognition sequence on a nucleic acid molecule that participates in an integration/recombination reaction by recombination proteins. Recombination sites are discrete sections or segments of nucleic acid on the participating nucleic acid molecules that are recognized and bound by a site-specific recombination protein during the initial stages of integration or recombination. For example, the recombination site for Cre recombinase is loxP, which is a 34 base pair sequence comprised of two 13 base pair inverted repeats (serving as the recombinase binding sites) flanking an 8 base pair core sequence (see FIG. 1 of Sauer, B., Curr. Opin. Biotech. 5:521-527 (1994)). Other examples of recombination sites include the attB, attP, attL, and attR sequences described in U.S. provisional patent applications 60/136,744, filed May 28, 1999, and 60/188,000, filed Mar. 9, 2000, and in co-pending U.S. patent application Ser. Nos. 09/517,466 and 09/732,91—all of which are specifically incorporated herein by reference—and mutants, fragments, variants and derivatives thereof, which are recognized by the recombination protein λ Int and by the auxiliary proteins integration host factor (IHF), FIS and excisionase (Xis) (see Landy, Curr. Opin. Biotech. 3:699-707 (1993)).
Recombination sites may be added to molecules by any number of known methods. For example, recombination sites can be added to nucleic acid molecules by blunt end ligation, PCR performed with fully or partially random primers, or inserting the nucleic acid molecules into an vector using a restriction site flanked by recombination sites.
Topoisomerase recognition site. As used herein, the term “topoisomerase recognition site” or “topoisomerase site” means a defined nucleotide sequence that is recognized and bound by a site specific topoisomerase. For example, the nucleotide sequence 5′-(C/T)CCTT-3′ is a topoisomerase recognition site that is bound specifically by most poxvirus topoisomerases, including vaccinia virus DNA topoisomerase I, which then can cleave the strand after the 3′-most thymidine of the recognition site to produce a nucleotide sequence comprising 5′-(C/T)CCTT-PO4-TOPO, i.e., a complex of the topoisomerase covalently bound to the 3′ phosphate through a tyrosine residue in the topoisomerase (see Shuman, J. Biol. Chem. 266:11372-11379, 1991; Sekiguchi and Shuman, Nucl. Acids Res. 22:5360-5365, 1994; each of which is incorporated herein by reference; see, also, U.S. Pat. No. 5,766,891; PCT/US95/16099; and PCT/US98/12372 also incorporated herein by reference). In comparison, the nucleotide sequence 5′-GCAACTT-3′ is the topoisomerase recognition site for type IA E. coli topoisomerase III.
Recombinational Cloning: As used herein, the phrase “recombinational cloning” refers to a method, such as that described in U.S. Pat. Nos. 5,888,732; 6,143,557; 6,171,861; 6,270,969; and 6,277,608 (the contents of which are fully incorporated herein by reference), whereby segments of nucleic acid molecules or populations of such molecules are exchanged, inserted, replaced, substituted or modified, in vitro or in vivo. In many instances, the cloning method is an in vitro method.
Cloning systems that utilize recombination at defined recombination sites have been previously described in U.S. Pat. No. 5,888,732, U.S. Pat. No. 6,143,557, U.S. Pat. No. 6,171,861, U.S. Pat. No. 6,270,969, and U.S. Pat. No. 6,277,608, and in pending U.S. application Ser. No. 09/517,466 filed Mar. 2, 2000, and in published United States application no. 2002 0007051-A1, all assigned to the Invitrogen Corporation, Carlsbad, Calif., the disclosures of which are specifically incorporated herein in their entirety. In brief, the G
Mutating specific residues in the core region of the att site can generate a large number of different att sites. As with the att1 and att2 sites utilized in G
Reaction Buffers: The invention further includes reaction buffers for performing recombination reactions (e.g., L×R reaction, B×P reactions, etc.) and reaction mixtures which comprise such reaction buffer, as well as methods employing reaction buffers of the invention for performing recombination reactions and products of recombination reactions produced using such reaction buffers. The components of an enzyme mix for performing B×P reactions may include phage-encoded Integrase (Int) protein as well as Integration Host Factor (IHF). The components of an enzyme mix for performing L×R reactions may include Int, IHF, and Exisionase (Xis).
Typically, reaction buffers of the invention will contain one or more of the following components: (1) one or more buffering agent (e.g., sodium phosphate, sodium acetate, 2-(N-moropholino)-ethanesulfonic acid (MES), tris-(hydroxymethyl)aminomethane (Tris), 3-(cyclohexylamino)-2-hydroxy-1-propanesulfonic acid (CAPS), citrate, N-2-hydroxyethylpiperazine-N′-2-ethanesulfonic acid (HEPES), acetate, 3-(N-morpholino)propanesulfonic acid (MOPS), N-tris(hydroxymethyl)methyl-3-aminopropanesulfonio acid (TAPS), etc.), (2) one or more salt (e.g., NaCl, KCl, etc.), (3) one or more chelating agent (e.g., one of more chelating agent which predominantly chelate divalent metal ions such as EDTA or EGTA), (4) one or more polyamine (e.g., spermidine, spermine, etc.), (5) one or more protein which is not typically directly involved in recombination reactions (e.g., BSA, ovalbumin, etc.), or (6) one or more diluent (e.g., water).
The concentration of the buffering agent in the reaction buffer of the invention will vary with the particular buffering agent used. Typically, the working concentration (i.e., the concentration in the reaction mixture) of the buffering agent will be from about 5 mM to about 500 mM (e.g., about 10 mM, about 15 mM, about 20 mM, about 25 mM, about 30 mM, about 35 mM, about 40 mM, about 45 mM, about 50 mM, about 55 mM, about 60 mM, about 65 mM, about 70 mM, about 75 mM, about 80 mM, about 85 mM, about 90 mM, about 95 mM, about 100 mM, from about 5 mM to about 500 mM, from about 10 mM to about 500 mM, from about 20 mM to about 500 mM, from about 25 mM to about 500 mM, from about 30 mM to about 500 mM, from about 40 mM to about 500 mM, from about 50 mM to about 500 mM, from about 75 mM to about 500 mM, from about 100 mM to about 500 mM, from about 25 mM to about 50 mM, from about 25 mM to about 75 mM, from about 25 mM to about 100 mM, from about 25 mM to about 200 mM, from about 25 mM to about 300 mM, etc.). When Tris (e.g., Tris-HCl) is used, the Tris working concentration will typically be from about 5 mM to about 100 mM, from about 5 mM to about 75 mM, from about 10 mM to about 75 mM, from about 10 mM to about 60 mM, from about 10 mM to about 50 mM, from about 25 mM to about 50 mM, etc.
The final pH of solutions of the invention will generally be set and maintained by buffering agents present in reaction buffers of the invention. The pH of reaction buffers of the invention, and hence reaction mixtures of the invention, will vary with the particular use and the buffering agent present but will often be from about pH 5.5 to about pH 9.0 (e.g., about pH 6.0, about pH 6.5, about pH 7.0, about pH 7.1, about pH 7.2, about pH 7.3, about pH 7.4, about pH 7.5, about pH 7.6, about pH 7.7, about pH 7.8, about pH 7.9, about pH 8.0, about pH 8.1, about pH 8.5, about pH 9.0, from about pH 6.0 to about pH 8.5, from about pH 6.5 to about pH 8.5, from about pH 7.0 to about pH 8.5, from about pH 7.5 to about pH 8.5, from about pH 6.0 to about pH 8.0, from about pH 6.0 to about pH 7.7, from about pH 6.0 to about pH 7.5, from about pH 6.0 to about pH 7.0, from about pH 7.2 to about pH 7.7, from about pH 7.3 to about pH 7.7, from about pH 7.4 to about pH 7.6, from about pH 7.0 to about pH 7.4, from about pH 7.6 to about pH 8.0, from about pH 7.6 to about pH 8.5, etc.)
As indicated, one or more salts (e.g., NaCl, KCl, etc.) may be included in reaction buffers of the invention. In many instances, salts used in reaction buffers of the invention will dissociate in solution to generate at least one species which is monovalent (e.g., Na+, K+, etc.) When included in reaction buffers of the invention, salts will often be present either individually or in a combined concentration of from about 0.5 mM to about 500 mM (e.g., about 1 mM, about 2 mM, about 3 mM, about 5 mM, about 10 mM, about 12 mM, about 15 mM, about 17 mM, about 20 mM, about 22 mM, about 23 mM, about 24 mM, about 25 mM, about 27 mM, about 30 mM, about 35 mM, about 40 mM, about 45 mM, about 50 mM, about 55 mM, about 60 mM, about 64 mM, about 65 mM, about 70 mM, about 75 mM, about 80 mM, about 85 mM, about 90 mM, about 95 mM, about 100 mM, about 120 mM, about 140 mM, about 150 mM, about 175 mM, about 200 mM, about 225 mM, about 250 mM, about 275 mM, about 300 mM, about 325 mM, about 350 mM, about 375 mM, about 400 mM, from about 1 mM to about 500 mM, from about 5 mM to about 500 mM, from about 10 mM to about 500 mM, from about 20 mM to about 500 mM, from about 30 mM to about 500 mM, from about 40 mM to about 500 mM, from about 50 mM to about 500 mM, from about 60 mM to about 500 mM, from about 65 mM to about 500 mM, from about 75 mM to about 500 mM, from about 85 mM to about 500 mM, from about 90 mM to about 500 mM, from about 100 mM to about 500 mM, from about 125 mM to about 500 mM, from about 150 mM to about 500 mM, from about 200 mM to about 500 mM, from about 10 mM to about 100 mM, from about 10 mM to about 75 mM, from about 10 mM to about 50 mM, from about 20 mM to about 200 mM, from about 20 mM to about 150 mM, from about 20 mM to about 125 mM, from about 20 mM to about 100 mM, from about 20 mM to about 80 mM, from about 20 mM to about 75 mM, from about 20 mM to about 60 mM, from about 20 mM to about 50 mM, from about 30 mM to about 500 mM, from about 30 mM to about 100 mM, from about 30 mM to about 70 mM, from about 30 mM to about 50 mM, etc.).
As also indicated above, one or more agents which chelate metal ions (e.g., monovalent or divalent metal ions) with relatively high affinity may also be present in reaction buffers of the invention. Examples of compounds which chelate metal ions with relatively high affinity include ethylenediamine tetraacetic acid (EDTA), diethylenetriaminepentaacetic acid (DTPA), triethylenetetraamine hexaacetic acid (TTHA), ethylenebis(oxyethylenenitrilo)]tetraacetic acid (EGTA), and propylenetriaminepentaacetic acid (PTPA). The free acid or salt of chelating agents may be used to prepare reaction buffers of the invention.
When included in reaction buffers of the invention, chelating agents will often be present either individually or in a combined concentration of from about 0.1 mM to about 50 mM (e.g., about 0.2 mM, about 0.3 mM, about 0.5 mM, about 0.7 mM, about 0.9 mM, about 1 mM, about 2 mM, about 3 mM, about 4 mM, about 5 mM, about 6 mM, about 10 mM, about 12 mM, about 15 mM, about 17 mM, about 20 mM, about 22 mM, about 23 mM, about 24 mM, about 25 mM, about 27 mM, about 30 mM, about 35 mM, about 40 mM, about 45 mM, about 50 mM, from about 0.1 mM to about 50 mM, from about 0.5 mM to about 50 mM, from about 1 mM to about 50 mM, from about 2 mM to about 50 mM, from about 3 mM to about 50 mM, from about 0.5 mM to about 20 mM, from about 0.5 mM to about 10 mM, from about 0.5 mM to about 5 mM, from about 0.5 mM to about 2.5 mM, from about 1 mM to about 20 mM, from about 1 mM to about 10 mM, from about 1 mM to about 5 mM, from about 1 mM to about 3.4 mM, from about 0.5 mM to about 3.0 mM, from about 1 mM to about 3.0 mM, from about 1.5 mM to about 3.0 mM, from about 2 mM to about 3.0 mM, from about 0.5 mM to about 2.5 mM, from about 1 mM to about 2.5 mM, from about 1.5 mM to about 2.5 mM, from about 2 mM to about 3.0 mM, from about 2.5 mM to about 3.0 mM, from about 0.5 mM to about 2 mM, from about 0.5 mM to about 1.5 mM, from about 0.5 mM to about 1.1 mM, etc.)
Reaction buffers of the invention may also contain one or more polyamine (e.g., spermine, spermidine, protamine, polylysine, and polyethylenimine, etc.), which may be synthetic or naturally occurring. When included in reaction buffers of the invention, polyamines will often be present either individually or in a combined concentration of from about 0.1 mM to about 50 mM (e.g., about 0.2 mM, about 0.3 mM, about 0.5 mM, about 0.7 mM, about 0.9 mM, about 1 mM, about 2 mM, about 3 mM, about 4 mM, about 5 mM, about 6 mM, about 6.5 mM, about 7 mM, about 7.5 mM, about 8 mM, about 8.5 mM, about 9 mM, about 9.5 mM, about 10 mM, about 12 mM, about 15 mM, about 17 mM, about 20 mM, about 22 mM, about 23 mM, about 24 mM, about 25 mM, about 27 mM, about 30 mM, about 35 mM, about 40 mM, about 45 mM, about 50 mM, from about 0.1 mM to about 50 mM, from about 0.5 mM to about 50 mM, from about 1 mM to about 50 mM, from about 2 mM to about 50 mM, from about 3 mM to about 50 mM, from about 0.5 mM to about 20 mM, from about 0.5 mM to about 10 mM, from about 0.5 mM to about 5 mM, from about 0.5 mM to about 2.5 mM, from about 1 mM to about 20 mM, from about 1 mM to about 10 mM, from about 1 mM to about 5 mM, from about 1 mM to about 3.4 mM, from about 0.5 mM to about 3.0 mM, from about 1 mM to about 3.0 mM, from about 1.5 mM to about 3.0 mM, from about 2 mM to about 3.0 mM, from about 0.5 mM to about 2.5 mM, from about 1 mM to about 2.5 mM, from about 1.5 mM to about 2.5 mM, from about 2 mM to about 3.0 mM, from about 2.5 mM to about 3.0 mM, from about 0.5 mM to about 2 mM, from about 0.5 mM to about 1.5 mM, from about 0.5 mM to about 1.1 mM, from about 7.6 mM to about 20 mM, from about 7.7 mM to about 20 mM, from about 7.8 mM to about 20 mM, from about 8.0 mM to about 20 mM, from about 8.1 mM to about 20 mM, from about 8.2 mM to about 20 mM, from about 8.3 mM to about 20 mM, from about 8.4 mM to about 20 mM, from about 8.5 mM to about 20 mM, from about 9.0 mM to about 20 mM, from about 10.0 mM to about 20 mM, from about 12.0 mM to about 20 mM, from about 7.6 mM to about 50 mM, from about 8.0 mM to about 50 mM, etc.). For example, reaction buffers of the invention may contain spermidine at a concentration of from about 7.6 mM to about 20 mM, from about 7.7 mM to about 20 mM, from about 7.8 mM to about 20 mM, from about 8.0 mM to about 20 mM, from about 8.1 mM to about 20 mM, from about 8.2 mM to about 20 mM, from about 8.3 mM to about 20 mM, from about 8.4 mM to about 20 mM, from about 8.5 mM to about 20 mM, from about 9.0 mM to about 20 mM, from about 10.0 mM to about 20 mM, from about 12.0 mM to about 20 mM, from about 7.6 mM to about 50 mM, from about 8.0 mM to about 50 mM, etc.
Reaction buffers of the invention may also contain one or more protein which is not typically directly involved in recombination reactions (e.g., bovine serum albumin (BSA); ovalbumin; immunoglobins, such as IgE, IgG, IgD; etc.). When included in reaction buffers of the invention, such proteins will often be present either individually or in a combined concentration of from about 0.1 mg/ml to about 50 mg/ml (e.g., about 0.1 mg/ml, about 0.2 mg/ml, about 0.3 mg/ml, about 0.4 mg/ml, about 0.5 mg/ml, about 0.6 mg/ml, about 0.7 mg/ml, about 0.8 mg/ml, about 0.9 mg/ml, about 1.0 mg/ml, about 1.1 mg/ml, about 1.3 mg/ml, about 1.5 mg/ml, about 1.7 mg/ml, about 2.0 mg/ml, about 2.5 mg/ml, about 3.5 mg/ml, about 5.0 mg/ml, about 7.5 mg/ml, about 10 mg/ml, about 15 mg/ml, about 20 mg/ml, about 25 mg/ml, about 30 mg/ml, about 35 mg/ml, about 40 mg/ml, from about 0.5 mg/ml to about 30 mg/ml, from about 0.75 mg/ml to about 30 mg/ml, from about 1.0 mg/ml to about 30 mg/ml, from about 2.0 mg/ml to about 30 mg/ml, from about 3.0 mg/ml to about 30 mg/ml, from about 4.0 mg/ml to about 30 mg/ml, from about 5.0 mg/ml to about 30 mg/ml, from about 7.5 mg/ml to about 30 mg/ml, from about 10 mg/ml to about 30 mg/ml, from about 15 mg/ml to about 30 mg/ml, from about 0.5 mg/ml to about 20 mg/ml, from about 0.5 mg/ml to about 10 mg/ml, from about 0.5 mg/ml to about 5 mg/ml, from about 0.5 mg/ml to about 2 mg/ml, from about 0.5 mg/ml to about 1 mg/ml, from about 1 mg/ml to about 10 mg/ml, from about 1 mg/ml to about 5 mg/ml, from about 1 mg/ml to about 2 mg/ml, etc.).
Examples of reaction buffers of the invention include the following: (1) 50 mM Tris-HCl (pH 7.5), 1 mM EDTA, 1 mg/ml BSA, 64 mM NaCl, 8 mM spermidine; (2) 50 mM Tris-HCl (pH 7.5), 1 mM EDTA, 1 mg/ml BSA, 64 mM NaCl, 10 mM spermidine; (3) 50 mM Tris-HCl (pH 7.5), 1 mM EDTA, 1 mg/ml BSA, 64 mM NaCl, 12 mM spermidine; (4) 50 mM Tris-HCl (pH 7.5), 1 mM EDTA, 1 mg/ml BSA, 75 mM NaCl, 8 mM spermidine; (5) 50 mM Tris-HCl (pH 7.5), 1 mM EDTA, 1 mg/ml BSA, 64 mM NaCl, 15 mM spermidine; (5) 25 mM Tris-HCl (pH 7.5), 1 mM EDTA, 1 mg/ml BSA, 64 mM NaCl, 8 mM spermidine; (7) 50 mM Tris-HCl (pH 7.5), 1 mM EDTA, 2 mg/ml BSA, 64 mM NaCl, 8 mM spermidine; (8) 25 mM Tris-HCl (pH 7.5), 5 mM EDTA, 1 mg/ml BSA, 64 mM NaCl, 8 mM spermidine; (9) 25 mM Tris-HCl (pH 7.5), 1 mM EDTA, 2 mg/ml BSA, 64 mM NaCl, 8 mM spermidine; (10) 100 mM Tris-HCl (pH 7.5), 1 mM EDTA, 1 mg/ml BSA, 64 mM NaCl, 10 mM spermidine; (11) 75 mM Tris-HCl (pH 7.5), 1 mM EDTA, 1 mg/ml BSA, 65 mM NaCl, 8 mM spermidine; (12) 50 mM Tris-HCl (pH 7.5), 1 mM EDTA, 1 mg/ml BSA, 64 mM NaCl, 8 mM spermine; (13) 50 mM Tris-HCl (pH 7.5), 1 mM EDTA, 1 mg/ml BSA, 65 mM NaCl, 8 mM spermidine; (14) 50 mM Tris-HCl (pH 7.5), 1 mM EDTA, 1 mg/ml BSA, 64 mM KCl, 8 mM spermidine; and (15) 75 mM Tris-HCl (pH 7.5), 1 mM EDTA, 1 mg/ml BSA, 64 mM KCl, 8 mM spermidine.
Reaction buffers of the invention may be prepared as concentrated solutions which are diluted to a working concentration for final use. For example, a reaction buffer of the invention may be prepared as a 5× concentrate with the following working concentrations of components being 50 mM Tris-HCl (pH 7.5), 1 mM EDTA, 1 mg/ml BSA, 64 mM NaCl, 8 mM spermidine. Such a 5× solution would contain 200 mM Tris-HCl (pH 7.5), 5 mM EDTA, 5 mg/ml BSA, 325 mM NaCl, and 40 mM spermidine. As another example, a reaction buffer of the invention for performing a LR reaction may be prepared as a 5× concentrate with the following working concentrations of components being 30 mM Tris-HCl (pH 7.4), 4.05 mM EDTA, 0.84 mg/ml BSA, 27.6 mM NaCl, 4.5 mM spermidine, 10% glycerol, 4.4 μg/ml Int, 1.5 μg/ml IHF, and 0.82 μg/ml Xis. Such a 5× solution would contain 150 mM Tris-HCl (pH 7.4), 20.25 mM EDTA, 4.2 mg/ml BSA, 138 mM NaCl, 22.5 mM spermidine, 50% glycerol, 22 μg/ml Int, 7.5 μg/ml IHF, and 4.1 μg/ml Xis. As yet another example, a reaction buffer of the invention for performing a BP reaction may be prepared as a 5× concentrate with the following working concentrations of components being 25 mM Tris-HCl (pH 7.4), 5 mM EDTA, 1 mg/ml BSA, 22 mM NaCl, 5 mM spermidine, 0.2 mM dithiothreitol (DTT), 0.0005% T
In some instances, the recombination reaction mixture buffer contain all of the components necessary for performing the reaction except for the nucleic acid. For example, recombination reaction mixtures will be started by adding the nucleic acids to be recombined, which may be added in one solution or in two different solutions. In many instances, the nucleic acids which are added to the reaction mixture buffer will be in water.
In many instances, reaction buffers of the invention will be provided in sterile form. Sterilization may be performed on the individual components of reaction buffers prior to mixing or on reaction buffers after they are prepared. Sterilization of such solutions may be performed by any suitable means including autoclaving or ultrafiltration.
Nucleic acid molecules used in methods of the invention, as well as those prepared by methods of the invention, may be dissolved in an aqueous buffer and added to the reaction mixture. One suitable set of conditions is 4 μl CLONASE™ enzyme mixture (e.g., Invitrogen Corporation, Cat. Nos. 11791-019 and 11789-013), 4 μl 5× reaction buffer and nucleic acid and water to a final volume of 20 μl. This will typically result in the inclusion of about 200 ng of Int and about 80 ng of IHF in a 20 μl BP reaction and about 150 ng Int, about 25 ng IHF and about 30 ng Xis in a 20 μl LR reaction.
Additional suitable sets of conditions include the use of smaller reaction volumes, for example, 2 μl CLONASE™ enzyme mixture (e.g., Invitrogen Corporation, Cat. Nos. 11791-019 and 11789-013), 2 μl 5× reaction buffer and nucleic acid and water to a final volume of 10 μl. In other embodiments, a suitable set of conditions includes 2 μl CLONASE™ enzyme mixture (e.g., Invitrogen Corporation, Cat. Nos. 11791-019 and 11789-013), 1 μl 10× reaction buffer and nucleic acid and water to a final volume of 10
Proteins for conducting an LR reaction may be stored in a suitable buffer, for example, LR Storage Buffer, which may comprise about 50 mM Tris at about pH 7.5, about 50 mM NaCl, about 0.25 mM EDTA, about 2.5 mM spermidine, and about 0.2 mg/ml BSA. When stored, proteins for an LR reaction may be stored at a concentration of about 37.5 ng/μl INT, 10 ng/μl IHF and 15 ng/μl XIS. Proteins for conducting a BP reaction may be stored in a suitable buffer, for example, BP Storage Buffer, which may comprise about 25 mM Tris at about pH 7.5, about 22 mM NaCl, about 5 mM EDTA, about 5 mM spermidine, about 1 mg/ml BSA, and about 0.0025% T
A suitable 5× reaction buffer for conducting recombination reactions may comprise 100 mM Tris pH 7.5, 88 mM NaCl, 20 mM EDTA, 20 mM spermidine, and 4 mg/ml BSA. Thus, in a recombination reaction, the final buffer concentrations may be 20 mM Tris pH 7.5, 17.6 mM NaCl, 4 mM EDTA, 4 mM spermidine, and 0.8 mg/ml BSA. Those skilled in the art will appreciate that the final reaction mixture may incorporate additional components added with the reagents used to prepare the mixture, for example, a BP reaction may include 0.005% T
In additional embodiments, a 10× reaction buffer for conducting recombination reactions may be prepared and comprise 200 mM Tris pH 7.5, 176 mM NaCl, 40 mM EDTA, 40 mM spermidine, and 8 mg/ml BSA. Thus, in a recombination reaction, the final buffer concentrations may be 20 mM Tris pH 7.5, 17.6 mM NaCl, 4 mM EDTA, 4 mM spermidine, and 0.8 mg/ml BSA. Those skilled in the art will appreciate that the final reaction mixture may incorporate additional components added with the reagents used to prepare the mixture, for example, a BP reaction may include 0.01% T
In particular embodiments, particularly those in which attL sites are to be recombined with attR sites, the final reaction mixture may include about 50 mM Tris HCl, pH 7.5, about 1 mM EDTA, about 1 mg/ml BSA, about 75 mM NaCl and about 7.5 mM spermidine in addition to recombination enzymes and the nucleic acids to be combined. In other embodiments, particularly those in which an attB site is to be recombined with an attP site, the final reaction mixture may include about 25 mM Tris HCl, pH 7.5, about 5 mM EDTA, about 1 mg/ml bovine serum albumin (BSA), about 22 mM NaCl, and about 5 mM spermidine.
In some embodiments, particularly those in which attL sites are to be recombined with attR sites, the final reaction mixture may include about 40 mM Tris HCl, pH 7.5, about 1 mM EDTA, about 1 mg/ml BSA, about 64 mM NaCl and about 8 mM spermidine in addition to recombination enzymes and the nucleic acids to be combined. One of skill in the art will appreciate that the reaction conditions may be varied somewhat without departing from the invention. For example, the pH of the reaction may be varied from about 7.0 to about 8.0; the concentration of buffer may be varied from about 25 mM to about 100 mM; the concentration of EDTA may be varied from about 0.5 mM to about 2 mM; the concentration of NaCl may be varied from about 25 mM to about 150 mM; and the concentration of BSA may be varied from 0.5 mg/ml to about 5 mg/ml. In other embodiments, particularly those in which an attB site is to be recombined with an attP site, the final reaction mixture may include about 25 mM Tris HCl, pH 7.5, about 5 mM EDTA, about 1 mg/ml bovine serum albumin (BSA), about 22 mM NaCl, about 5 mM spermidine and about 0.005% detergent (e.g., T
In other embodiments, the recombination reactions may be prepared using a buffer which performs the functions of both the storage and reaction buffers in one. Suitably, in such embodiments, this buffer may comprise between about 100-200 mM Tris pH 7.5, between about 88-176 mM NaCl, between about 20-40 mM EDTA, between about 20-40 mM spermidine, and between about 4-8 mg/ml BSA. Those skilled in the art will appreciate that the final reaction mixture may incorporate additional components added with the reagents used to prepare the mixture, for example, a BP reaction may include between about 0.005-0.01% T
The amount of nucleic acid which is the subject of recombination reactions may vary considerably. Typically, the amount of nucleic acid present in a 10 μl final reaction mixture will be between 50 and 500 ng, 10 and 500 ng, 25 and 500 ng, 75 and 500 ng, 100 and 500 ng, 200 and 500 ng, 300 and 500 ng, 50 and 300 ng, 50 and 250 ng, 250 and 500 ng, or 50 and 400 ng. Further, the nucleic acids which are the subject of the recombination reaction need not be present in equal amounts. For example, when two nucleic acids are to be recombined, they may be present in an amount defined by a ratio of 1:1.1, 1:1.2, 1:1.3, 1:1.4, 1:1.5, 1:2.0. 1:2.5, or 1:3.0.
Repression Cassette: As used herein, the phrase “repression cassette” refers to a nucleic acid segment that contains a repressor or a selectable marker present in the subcloning vector.
Selectable Marker: As used herein, the phrase “selectable marker” refers to a nucleic acid segment that allows one to select for or against a molecule (e.g., a replicon) or a cell that contains it and/or permits identification of a cell or organism that contains or does not contain the nucleic acid segment. Frequently, selection and/or identification occur under particular conditions and do not occur under other conditions.
Markers can encode an activity, such as, but not limited to, production of RNA, peptide, or protein, or can provide a binding site for RNA, peptides, proteins, inorganic and organic compounds or compositions and the like. Examples of selectable markers include but are not limited to: (1) nucleic acid segments that encode products that provide resistance against otherwise toxic compounds (e.g., antibiotics); (2) nucleic acid segments that encode products that are otherwise lacking in the recipient cell (e.g., tRNA genes, auxotrophic markers); (3) nucleic acid segments that encode products that suppress the activity of a gene product; (4) nucleic acid segments that encode products that can be readily identified (e.g., phenotypic markers such as β-lactamase, β-galactosidase, green fluorescent protein (GFP), yellow flourescent protein (YFP), red fluorescent protein (RFP), cyan fluorescent protein (CFP), and cell surface proteins); (5) nucleic acid segments that bind products that are otherwise detrimental to cell survival and/or function; (6) nucleic acid segments that otherwise inhibit the activity of any of the nucleic acid segments described in Nos. 1-5 above (e.g., antisense oligonucleotides); (7) nucleic acid segments that bind products that modify a substrate (e.g., restriction endonucleases); (8) nucleic acid segments that can be used to isolate or identify a desired molecule (e.g., specific protein binding sites); (9) nucleic acid segments that encode a specific nucleotide sequence that can be otherwise non-functional (e.g., for PCR amplification of subpopulations of molecules); (10) nucleic acid segments that, when absent, directly or indirectly confer resistance or sensitivity to particular compounds; and/or (11) nucleic acid segments that encode products that either are toxic (e.g., Diphtheria toxin) or convert a relatively non-toxic compound to a toxic compound (e.g., Herpes simplex thymidine kinase, cytosine deaminase) in recipient cells; (12) nucleic acid segments that inhibit replication, partition or heritability of nucleic acid molecules that contain them; and/or (13) nucleic acid segments that encode conditional replication functions, e.g., replication in certain hosts or host cell strains or under certain environmental conditions (e.g., temperature, nutritional conditions, etc.).
Selection and/or identification may be accomplished using techniques well known in the art. For example, a selectable marker may confer resistance to an otherwise toxic compound and selection may be accomplished by contacting a population of host cells with the toxic compound under conditions in which only those host cells containing the selectable marker are viable. In another example, a selectable marker may confer sensitivity to an otherwise benign compound and selection may be accomplished by contacting a population of host cells with the benign compound under conditions in which only those host cells that do not contain the selectable marker are viable. A selectable marker may make it possible to identify host cells containing or not containing the marker by selection of appropriate conditions. In one aspect, a selectable marker may enable visual screening of host cells to determine the presence or absence of the marker. For example, a selectable marker may alter the color and/or fluorescence characteristics of a cell containing it. This alteration may occur in the presence of one or more compounds, for example, as a result of an interaction between a polypeptide encoded by the selectable marker and the compound (e.g., an enzymatic reaction using the compound as a substrate). Such alterations in visual characteristics can be used to physically separate the cells containing the selectable marker from those not contain it by, for example, fluorescent activated cell sorting (FACS).
Multiple selectable markers may be simultaneously used to distinguish various populations of cells. For example, a nucleic acid molecule of the invention may have multiple selectable markers, one or more of which may be removed from the nucleic acid molecule by a suitable reaction (e.g., a recombination reaction). After the reaction, the nucleic acid molecules may be introduced into a host cell population and those host cells comprising nucleic acid molecules having all of the selectable markers may be distinguished from host cells comprising nucleic acid molecules in which one or more selectable markers have been removed (e.g., by the recombination reaction). For example, a nucleic acid molecule of the invention may have a blasticidin resistance marker outside a pair of recombination sites and a β-lactamase encoding selectable marker inside the recombination sites. After a recombination reaction and introduction of the reaction mixture into a cell population, cells comprising any nucleic acid molecule can be selected for by contacting the cell population with blasticidin. Those cell comprising a nucleic acid molecule that has undergone a recombination reaction can be distinguished from those containing an unreacted nucleic acid molecules by contacting the cell population with a fluorogenic β-lactamase substrate as described below and observing the fluorescence of the cell population. Optionally, the desired cells can be physically separated from undesirable cells, for example, by FACS.
Selection Scheme: As used herein, the phrase “selection scheme” refers to any method that allows selection, enrichment, or identification of a desired nucleic acid molecules or host cells containing them (in particular Product or Product(s) from a mixture containing an Entry Clone or Vector, a Destination Vector, a Donor Vector, an Expression Clone or Vector, any intermediates (e.g., a Cointegrate or a replicon), and/or Byproducts). In one aspect, selection schemes of the invention rely on one or more selectable markers. The selection schemes of one embodiment have at least two components that are either linked or unlinked during recombinational cloning. One component is a selectable marker. The other component controls the expression in vitro or in vivo of the selectable marker, or survival of the cell (or the nucleic acid molecule, e.g., a replicon) harboring the plasmid carrying the selectable marker. Generally, this controlling element will be a repressor or inducer of the selectable marker, but other means for controlling expression or activity of the selectable marker can be used. Whether a repressor or activator is used will depend on whether the marker is for a positive or negative selection, and the exact arrangement of the various nucleic acid segments, as will be readily apparent to those skilled in the art. In some embodiments, the selection scheme results in selection of, or enrichment for, only one or more desired nucleic acid molecules (such as Products). As defined herein, selecting for a nucleic acid molecule includes (a) selecting or enriching for the presence of the desired nucleic acid molecule (referred to as a “positive selection scheme”), and (b) selecting or enriching against the presence of nucleic acid molecules that are not the desired nucleic acid molecule (referred to as a “negative selection scheme”).
In one embodiment, the selection schemes (which can be carried out in reverse) will take one of three forms, which will be discussed in terms of
Examples of such toxic gene products are well known in the art, and include, but are not limited to, restriction endonucleases (e.g., DpnI, Nla3, etc.); apoptosis-related genes (e.g., ASK1 or members of the bcl-2/ced-9 family); retroviral genes; including those of the human immunodeficiency virus (HIV); defensins such as NP-1; inverted repeats or paired palindromic nucleic acid sequences; bacteriophage lytic genes such as those from ΦX174 or bacteriophage T4; antibiotic sensitivity genes such as rpsL; antimicrobial sensitivity genes such as pheS; plasmid killer genes' eukaryotic transcriptional vector genes that produce a gene product toxic to bacteria, such as GATA-1; genes that kill hosts in the absence of a suppressing function, e.g., kicB, ccdB, ΦX174 E (Liu, Q., et al., Curr. Biol. 8:1300-1309 (1998)); and other genes that negatively affect replicon stability and/or replication. A toxic gene can alternatively be selectable in vitro, e.g., a restriction site.
Many genes coding for restriction endonucleases operably linked to inducible promoters are known, and may be used in the present invention (see, e.g., U.S. Pat. Nos. 4,960,707 (DpnI and DpnII); 5,082,784 and 5,192,675 (KpnI); 5,147,800 (NgoAIII and NgoAI); 5,179,015 (FspI and HaeIII): 5,200,333 (HaeII and TaqI); 5,248,605 (HpaII); 5,312,746 (ClaI); 5,231,021 and 5,304,480 (XhoI and XhoII); 5,334,526 (AluI); 5,470,740 (NsiI); 5,534,428 (SstI/SacI); 5,202,248 (NcoI); 5,139,942 (NdeI); and 5,098,839 (Pad). (See also Wilson, G. G., Nucl. Acids Res. 19:2539-2566 (1991); and Lumen, K. D., et al., Gene 74:25-32 (1988)).
In the second form, segment D carries a selectable marker. The toxic gene would eliminate transformants harboring the Vector Donor, Cointegrate, and Byproduct molecules, while the selectable marker can be used to select for cells containing the Product and against cells harboring only the Insert Donor.
The third form selects for cells that have both segments A and D in cis on the same molecule, but not for cells that have both segments in trans on different molecules. This could be embodied by a selectable marker that is split into two inactive fragments, one each on segments A and D.
The fragments are so arranged relative to the recombination sites that when the segments are brought together by the recombination event, they reconstitute a functional selectable marker. For example, the recombinational event can link a promoter with a structural nucleic acid molecule (e.g., a gene), can link two fragments of a structural nucleic acid molecule, or can link nucleic acid molecules that encode a heterodimeric gene product needed for survival, or can link portions of a replicon.
Site-Specific Recombinase: As used herein, the phrase “site-specific recombinase” refers to a type of recombinase that typically has at least the following four activities (or combinations thereof): (1) recognition of specific nucleic acid sequences; (2) cleavage of said sequence or sequences; (3) topoisomerase activity involved in strand exchange; and (4) ligase activity to reseal the cleaved strands of nucleic acid (see Sauer, B., Current Opinions in Biotechnology 5:521-527 (1994)). Conservative site-specific recombination is distinguished from homologous recombination and transposition by a high degree of sequence specificity for both partners. The strand exchange mechanism involves the cleavage and rejoining of specific nucleic acid sequences in the absence of DNA synthesis (Landy, A. (1989) Ann. Rev. Biochem. 58:913-949).
Suppressor tRNA. As used herein, the phrase “suppressor tRNA” is used to indicate a tRNA molecule that results in the incorporation of an amino acid in a polypeptide in a position corresponding to a stop codon in the mRNA being translated.
Homologous Recombination: As used herein, the phrase “homologous recombination” refers to the process in which nucleic acid molecules with similar nucleotide sequences associate and exchange nucleotide strands. A nucleotide sequence of a first nucleic acid molecule that is effective for engaging in homologous recombination at a predefined position of a second nucleic acid molecule will therefore have a nucleotide sequence that facilitates the exchange of nucleotide strands between the first nucleic acid molecule and a defined position of the second nucleic acid molecule. Thus, the first nucleic acid will generally have a nucleotide sequence that is sufficiently complementary to a portion of the second nucleic acid molecule to promote nucleotide base pairing.
Homologous recombination requires homologous sequences in the two recombining partner nucleic acids but does not require any specific sequences. As indicated above, site-specific recombination that occurs, for example, at recombination sites such as att sites, is not considered to be “homologous recombination,” as the phrase is used herein.
Vector: As used herein, the term “vector” refers to a nucleic acid molecule (e.g., DNA) that provides a useful biological or biochemical property to an insert. Examples include plasmids, phages, autonomously replicating sequences (ARS), centromeres, and other sequences that are able to replicate or be replicated in vitro or in a host cell, or to convey a desired nucleic acid segment to a desired location within a host cell. A vector can have one or more recognition sites (e.g., two, three, four, five, seven, ten, etc. recombination sites, restriction sites, and/or topoisomerases sites) at which the sequences can be manipulated in a determinable fashion without loss of an essential biological function of the vector, and into which a nucleic acid fragment can be spliced in order to bring about its replication and cloning. Vectors can further provide primer sites (e.g., for PCR), transcriptional and/or translational initiation and/or regulation sites, recombinational signals, replicons, selectable markers, etc. Clearly, methods of inserting a desired nucleic acid fragment that do not require the use of recombination, transpositions or restriction enzymes (such as, but not limited to, uracil N-glycosylase (UDG) cloning of PCR fragments (U.S. Pat. Nos. 5,334,575 and 5,888,795, both of which are entirely incorporated herein by reference), T:A cloning, and the like) can also be applied to clone a fragment into a cloning vector to be used according to the present invention. The cloning vector can further contain one or more selectable markers (e.g., two, three, four, five, seven, ten, etc.) suitable for use in the identification of cells transformed with the cloning vector.
Subcloning Vector: As used herein, the phrase “subcloning vector” refers to a cloning vector comprising a circular or linear nucleic acid molecule that includes, in many instances, an appropriate replicon. In the present invention, the subcloning vector (segment D in
Vector Donor: As used herein, the phrase “Vector Donor” refers to one of the two parental nucleic acid molecules (e.g., RNA or DNA) of the present invention that carries the nucleic acid segments comprising the nucleic acid vector that is to become part of the desired Product. The Vector Donor comprises a subcloning vector D (or it can be called the cloning vector if the Insert Donor does not already contain a cloning vector) and a segment C flanked by recombination sites (see
Primer: As used herein, the term “primer” refers to a single stranded or double stranded oligonucleotide that is extended by covalent bonding of nucleotide monomers during amplification or polymerization of a nucleic acid molecule (e.g., a DNA molecule). In one aspect, the primer may be a sequencing primer (for example, a universal sequencing primer). In another aspect, the primer may comprise a recombination site or portion thereof.
Adapter: As used herein, the term “adapter” refers to an oligonucleotide or nucleic acid fragment or segment (e.g., DNA) that comprises one or more recombination sites and/or topoisomerase site (or portions of such sites) that can be added to a circular or linear Insert Donor molecule as well as to other nucleic acid molecules described herein. When using portions of sites, the missing portion may be provided by the Insert Donor molecule. Such adapters may be added at any location within a circular or linear molecule, although the adapters are typically added at or near one or both termini of a linear molecule. Adapters may be positioned, for example, to be located on both sides (flanking) a particular nucleic acid molecule of interest. In accordance with the invention, adapters may be added to nucleic acid molecules of interest by standard recombinant techniques (e.g., restriction digest and ligation). For example, adapters may be added to a circular molecule by first digesting the molecule with an appropriate restriction enzyme, adding the adapter at the cleavage site and reforming the circular molecule that contains the adapter(s) at the site of cleavage. In other aspects, adapters may be added by homologous recombination, by integration of RNA molecules, and the like. Alternatively, adapters may be ligated directly to one or more terminus or both termini of a linear molecule thereby resulting in linear molecule(s) having adapters at one or both termini. In one aspect of the invention, adapters may be added to a population of linear molecules, (e.g., a cDNA library or genomic DNA that has been cleaved or digested) to form a population of linear molecules containing adapters at one terminus or both termini of all or substantial portion of said population.
Adapter-Primer: As used herein, the phrase “adapter-primer” refers to a primer molecule that comprises one or more recombination sites (or portions of such recombination sites) that can be added to a circular or to a linear nucleic acid molecule described herein. When using portions of recombination sites, the missing portion may be provided by a nucleic acid molecule (e.g., an adapter) of the invention. Such adapter-primers may be added at any location within a circular or linear molecule, although the adapter-primers may be added at or near one or both termini of a linear molecule. Such adapter-primers may be used to add one or more recombination sites or portions thereof to circular or linear nucleic acid molecules in a variety of contexts and by a variety of techniques, including but not limited to amplification (e.g., PCR), ligation (e.g., enzymatic or chemical/synthetic ligation), recombination (e.g., homologous or non-homologous (illegitimate) recombination) and the like.
Template: As used herein, the term “template” refers to a double stranded or single stranded nucleic acid molecule that is to be amplified, synthesized or sequenced. In the case of a double-stranded DNA molecule, denaturation of its strands to form a first and a second strand may be performed before these molecules may be amplified, synthesized or sequenced, or the double stranded molecule may be used directly as a template. For single stranded templates, a primer complementary to at least a portion of the template hybridizes under appropriate conditions and one or more polypeptides having polymerase activity (e.g., two, three, four, five, or seven DNA polymerases and/or reverse transcriptases) may then synthesize a molecule complementary to all or a portion of the template. Alternatively, for double stranded templates, one or more transcriptional regulatory sequences (e.g., two, three, four, five, seven or more promoters) may be used in combination with one or more polymerases to make nucleic acid molecules complementary to all or a portion of the template. The newly synthesized molecule, according to the invention, may be of equal or shorter length compared to the original template. Mismatch incorporation or strand slippage during the synthesis or extension of the newly synthesized molecule may result in one or a number of mismatched base pairs. Thus, the synthesized molecule need not be exactly complementary to the template. Additionally, a population of nucleic acid templates may be used during synthesis or amplification to produce a population of nucleic acid molecules typically representative of the original template population.
Incorporating: As used herein, the term “incorporating” means becoming a part of a nucleic acid (e.g., DNA) molecule or primer.
Library: As used herein, the term “library” refers to a collection of nucleic acid molecules (circular or linear). In one embodiment, a library may comprise a plurality of nucleic acid molecules (e.g., two, three, four, five, seven, ten, twelve, fifteen, twenty, thirty, fifty, one hundred, two hundred, five hundred one thousand, five thousand, or more), that may or may not be from a common source organism, organ, tissue, or cell. In another embodiment, a library is representative of all or a portion or a significant portion of the nucleic acid content of an organism (a “genomic” library), or a set of nucleic acid molecules representative of all or a portion or a significant portion of the expressed nucleic acid molecules (a cDNA library or segments derived there from) in a cell, tissue, organ or organism. A library may also comprise nucleic acid molecules having random sequences made by de novo synthesis, mutagenesis of one or more nucleic acid molecules, and the like. Such libraries may or may not be contained in one or more vectors (e.g., two, three, four, five, seven, ten, twelve, fifteen, twenty, thirty, fifty, etc.).
Amplification: As used herein, the term “amplification” refers to any in vitro method for increasing the number of copies of a nucleic acid molecule with the use of one or more polypeptides having polymerase activity (e.g., one, two, three, four or more nucleic acid polymerases or reverse transcriptases). Nucleic acid amplification results in the incorporation of nucleotides into a DNA and/or RNA molecule or primer thereby forming a new nucleic acid molecule complementary to a template. The formed nucleic acid molecule and its template can be used as templates to synthesize additional nucleic acid molecules. As used herein, one amplification reaction may consist of many rounds of nucleic acid replication. DNA amplification reactions include, for example, polymerase chain reaction (PCR). One PCR reaction may consist of 5 to 100 cycles of denaturation and synthesis of a DNA molecule.
Nucleotide: As used herein, the term “nucleotide” refers to a base-sugar-phosphate combination. Nucleotides are monomeric units of a nucleic acid molecule (DNA and RNA). The term nucleotide includes ribonucleoside triphosphates ATP, UTP, CTG, GTP and deoxyribonucleoside triphosphates such as dATP, dCTP, dITP, dUTP, dGTP, dTTP, or derivatives thereof. Such derivatives include, for example, [α-S]dATP, 7-deaza-dGTP and 7-deaza-dATP. The term nucleotide as used herein also refers to dideoxyribonucleoside triphosphates (ddNTPs) and their derivatives. Illustrated examples of dideoxyribonucleoside triphosphates include, but are not limited to, ddATP, ddCTP, ddGTP, ddITP, and ddTTP. According to the present invention, a “nucleotide” may be unlabeled or detectably labeled by well known techniques. Detectable labels include, for example, radioactive isotopes, fluorescent labels, chemiluminescent labels, bioluminescent labels and enzyme labels.
Nucleic Acid Molecule: As used herein, the phrase “nucleic acid molecule” refers to a sequence of contiguous nucleotides (riboNTPs, dNTPs, ddNTPs, or combinations thereof) of any length. A nucleic acid molecule may encode a full-length polypeptide or a fragment of any length thereof, or may be non-coding. As used herein, the terms “nucleic acid molecule” and “polynucleotide” may be used interchangeably and include both RNA and DNA.
Oligonucleotide: As used herein, the term “oligonucleotide” refers to a synthetic or natural molecule comprising a covalently linked sequence of nucleotides that are joined by a phosphodiester bond between the 3′ position of the pentose of one nucleotide and the 5′ position of the pentose of the adjacent nucleotide.
Polypeptide: As used herein, the term “polypeptide” refers to a sequence of contiguous amino acids of any length. The terms “peptide,” “oligopeptide,” or “protein” may be used interchangeably herein with the term “polypeptide.”
Hybridization: As used herein, the terms “hybridization” and “hybridizing” refer to base pairing of two complementary single-stranded nucleic acid molecules (RNA and/or DNA) to give a double stranded molecule. As used herein, two nucleic acid molecules may hybridize, although the base pairing is not completely complementary. Accordingly, mismatched bases do not prevent hybridization of two nucleic acid molecules provided that appropriate conditions, well known in the art, are used. In some aspects, hybridization is said to be under “stringent conditions.” By “stringent conditions,” as the phrase is used herein, is meant overnight incubation at 42° C. in a solution comprising: 50% formamide, 5×SSC (750 mM NaCl, 75 m M trisodium citrate), 50 mM sodium phosphate (pH 7.6), 5×Denhardt's solution, 10% dextran sulfate, and 20 μg/ml denatured, sheared salmon sperm DNA, followed by washing the filters in 0.1×SSC at about 65° C.
Derivative: As used herein the term “derivative”, when used in reference to a vector, means that the derivative vector contains one or more (e.g., one, two, three, four five, etc.) nucleic acid segments which share sequence similar to at least one vector represented in one or more of
Other terms used in the fields of recombinant nucleic acid technology and molecular and cell biology as used herein will be generally understood by one of ordinary skill in the applicable arts.
The present invention relates to nucleic acid sequences encoding a polypeptide having a detectable activity, nucleic acid molecules comprising such sequences, and methods of joining nucleic acid molecules comprising such sequences to other nucleic acid molecules (which may comprise sequences encoding one or more polypeptides). The invention also relates to compositions comprising nucleic acid molecules of the invention, polypeptides (e.g., fusion polypeptides) encoded by such nucleic acid molecules, vectors comprising such nucleic acid molecules and derivatives thereof, and kits comprising such compositions.
The invention also includes nucleic acid molecules that encode fusion proteins comprising the following three polypeptide portions: (1) a polypeptide encoded by a nucleic acid of interest (e.g., a nucleic acid segment which has been inserted into a vector), (2) a peptide or polypeptide encoded by all or part of cloning site (e.g., a restriction enzyme recognition site, a recombination site, a topoisomerase recognition site, etc.), and (3) a polypeptide having a detectable activity. The invention further includes fusion proteins which are encoded by such nucleic acid molecules, as well as (a) methods for making such nucleic acid molecules and fusions proteins and (b) compositions (e.g., reaction mixtures) comprising such nucleic acid molecules and fusions proteins.
The polypeptide portions referred to above may be connected in any order to form fusion proteins of the invention but typical orders included (1)-(2)-(3) and (3)-(2)-(1). In particular instances, a peptide or polypeptide encoded by all or part of cloning site may comprise one to three, three to five, five to eight, eight to ten, ten to fifteen, or fourteen to twenty amino acids.
As noted above, one component of fusion proteins of the invention may be encoded by a cloning site, such as a topoisomerase recognition site. Exemplary topoisomerase recognition sites comprise the sequences CCCTT and TCCTT. Topoisomerase recognition sequences are five nucleotides in length. Depending upon the reading frame of the polypeptides on either side of the topoisomerase site, it may be desirable to add one or two nucleotides on either side of the site and introduce either a di- or tri-peptide into the final fusion protein. For example, one nucleotide may be added at either end of the topoisomerase site, for example, so that the site with the additional nucleotide encodes a di-peptide. For the topoisomerase recognition sequence CCCTT, the codon duplexes thus generated are ACC CTT (encoding Thr-Leu), GCC CTT, (encoding Ala-Leu), TCC CTT, (encoding Ser-Leu), CCC CTT, (encoding Pro-Leu), CCC TTA, (encoding Pro-Leu), CCC TTG, (encoding Pro-Leu), CCC TTT, (encoding Pro-Phe), and CCC TTC, (encoding Pro-Phe). In many organisms, the dipeptides encoded by these codon duplexes would be Thr-Leu, Ser-Leu, Pro-Leu, Ala-Leu, Pro-Leu, and Pro-Phe. Thus, fusion proteins of the invention include those which comprise the following polypeptide portions: (1)-Thr-Leu-(3), (3)-Thr-Leu-(1), (1)-Ser-Leu-(3), (3)-Ser-Leu-(1), (1)-Pro-Leu-(3), (3)-Pro-Leu-(1), (1)-Ala-Leu-(3), (3)-Ala-Leu-(1), (1)-Pro-Leu-(3), (3)-Pro-Leu-(1), (1)-Pro-Phe-(3), and (3)-Pro-Phe-(1).
In some embodiments, it may be desirable to add two nucleotides on either side of a topoisomerase site so as to bring polypeptides encoded on the nucleic acid molecules to be joined into the same reading frame. This may result in the addition of a tri-peptide to the final fusion protein. For example, if the polypeptide encoded by the nucleic acid molecule on one side of the topoisomerase site is in the first reading frame and the polypeptide encoded by the nucleic acid molecule on the other side of the topoisomerase site is in the third reading frame, it may be desirable to add two nucleotides to either side of the topoisomerase site (or equivalently to either nucleic acid molecule) to bring the polypeptides into the same reading frame. For example, in the sequence ATG-CCCTT-XXATG, the first ATG represents a polypeptide in the first reading frame of a first nucleic acid molecule CCCTT represents the nucleotides of the topoisomerase site and XXATG represents the nucleic acid sequence encoding a polypeptide in the third reading frame on the second nucleic acid molecule. In order to bring the two polypeptides into the same reading frame (i.e., put the ATG codons in the same reading frame) two nucleotides must be added to either side of the topoisomerase site or one to each side. When two nucleotides are added, for example, on the 3′ side of the topoisomerase site, the nucleic acid sequence and first two amino acids would be as above (i.e., CCC TTA, (encoding Pro-Leu), CCC TTG, (encoding Pro-Leu), CCC TTT, (encoding Pro-Phe), and CCC TTC, (encoding Pro-Phe) and the third amino acid could be any of the twenty naturally occurring amino acids depending upon the nucleotides one the second nucleic acid molecule (i.e., XX) and the second of the two nucleotides added. If the two nucleotides added are N1 and N2 the final nucleic acid molecule would have the sequence ATG-CCC-TTN1-N2XX-ATG. Thus, the tri-peptide may have the sequence Pro-(Phe or Leu)-Xaa where Xaa represents any of the naturally occurring amino acids. In like fashion, one skilled in the art can readily determine the peptide sequences generated by adding two nucleotides to the 5′-side of the topoisomerase site, or by adding one nucleotide to either side of the topoisomerase site. Fusion proteins comprising such sequences are within the scope of the present invention.
One example of an amino acid sequence which may be encoded by a cloning site is the following: Pro-Ala-Phe-Leu-Tyr-Lys-Val-Gly-Ile-Ile-Arg-Lys-His-Cys-Leu-Ser-Ile-Cys-Cys-Asn-Glu-Gln-Val-Thr-Ile-Ser-Gln-Asn-Lys-Ile-Ile-Ile (SEQ ID NO:56). This amino acid sequence is encoded by one of the six reading frames of an attL2 recombination site. This amino acid sequence may be present in fusion proteins due to the fact that there are no stop codons present in the reading of the attL2 site which encodes this amino acid sequence. Thus, when a fusion protein of the order (1)-(2)-(3) or (3)-(2)-(1) contains an attL2 site as the cloning site (i.e., component (2)). The amino acid sequence referred to above will often be encoded by an attL2 recombination site. Further this amino acid sequence may only comprise part of the amino acid sequence encoded by a portion of an attL2 recombination site. Thus, in particular embodiments, proteins of the invention will contain at least two, three, four, five, six, seven, eight, nine, ten, eleven, twelve, thirteen, fourteen, fifteen, sixteen, seventeen, eighteen, nineteen, twenty, twenty-five, or thirty amino acids of the sequence Pro-Ala-Phe-Leu-Tyr-Lys-Val-Gly-Ile-Ile-Arg-Lys-His-Cys-Leu-Ser-Ile-Cys-Cys-Asn-Glu-Gln-Val-Thr-Ile-Ser-Gln-Asn-Lys-Ile-Ile-Ile (SEQ ID NO:57). The invention further includes fusion proteins which contain a full-length amino acid sequence encoded by any of the six reading frames of any of the recombination sites set out in Table 4, as well as sub-portions of such amino acid sequences of the lengths set out above for the attL2 recombination site.
Polypeptides having a detectable activity which may be included in fusion proteins of the invention include those which function as reporters. Examples of suitable reporters are β-lactamases. When export of the fusion protein from the cell is not desired, β-lactamase polypeptides which may be used in methods and compositions of the invention will typically not contain a functional signal peptide. This is so because signal peptides of some β-lactamase polypeptides have been found to function in both eukaryotic and prokaryotic cells. In contrast, when export of the fusion protein from the cell is desired, β-lactamase polypeptides which may be used in methods and compositions of the invention may contain a functional signal peptide. Further, in such instances, the β-lactamase polypeptide portion of the fusion protein may be located at the amino-terminus.
Polypeptides having a detectable activity which may be included in fusion proteins of the invention include those which function as detectable tags or affinity tags. Examples of such tags include peptides such as those which have affinity for molecules containing one or more arsenic atoms (e.g., F
The invention further includes peptides which are designed to bind to or binds to biarsenical compounds, as well as nucleic acid which encodes such peptides and proteins which contain such peptides. Such peptides, as well as biarsenical compounds themselves, are described in U.S. Pat. No. 6,451,569, the entire disclosure of which is incorporated herein by reference. One specific example of a peptide of the invention, which may be referred to as a tag, is Ala-Gly-Gly-Cys-Cys-Pro-Gly-Cys-Cys-Gly-Gly-Gly (SEQ ID NO:61). The invention thus includes peptides comprising this sequence, proteins which contain this sequence, and nucleic acids which encode this sequence.
Nucleic acids of the invention include those which have been adapted to encode tags but have been modified to have one or more particular activities or lack one or more particular activities. As an example, the nucleotide sequence shown in Table 10 was designed to encodes a tag which binds biarsenical compounds and to avoid hairpin loops, palindromes, dimer formation and the use of any rare tRNA codons. Thus, nucleic acids of the invention may be designed or selected such that they have particular properties both at the nucleic acid and amino acid level. For example, nucleic acids of the invention may be designed or selected such that they encode particular amino acid sequences but also have particular properties as nucleic acids either themselves or upon transcription. For example, such nucleic acid may be designed or selected such that they either contain particular restriction sites or that they lack sequences which are often recognized by restriction endonucleases (e.g., palindromes).
When nucleic acids of the invention are designed, codons may be selected to encode particular amino acids. These codons vary, to some extent, with the translation system of the organism used but one example of a codon usage chart is set out below in Table 1. Codon selection is one example of a way that nucleic acids of the invention (e.g., nucleic acids which encode particular tags such as a tetracysteine sequence) may be designed to have one or more desired properties (e.g., containing particular restriction sites, avoiding rare codons for a particular organism, etc.).
The invention thus includes variations of the nucleotide sequence GCT GGT GGC TGT TGT CCT GGC TGT TGC GGT GGC GGC (SEQ ID NO:62), set out in Table 10, but which encode the same amino acid sequence. Examples of such sequences include the following: (1) GCC GGC GGC TGT TGT CCT GGC TGT TGC GGT GGC GGC (SEQ ID NO:63), (2) GCT GGT GGC TGC TGC CCT GGC TGT TGC GGT GGC GGC (SEQ ID NO:64), (3) GCT GGT GGC TGT TGT CCT GGC TGT TGC GGT GGC GGC (SEQ ID NO:65), and (4) GCT GGT GGC TGT TGT CCA GGC TGT TGC GGT GGC GGC (SEQ ID NO:66), as well as sub-portions of these nucleotide sequences which encode the amino acid sequence Cys-Cys-X-X-Cys-Cys (e.g., Cys-Cys-Pro-Gly-Cys-Cys (SEQ ID NO:67)), wherein “X” is any amino acid. In particular embodiments, nucleic acid which encodes a tag of the invention will not contain a particular nucleotide (e.g., adenosine, guanine, thymine, or cytosine). As an example, several of the nucleotide sequence shown above do not contain any adenosines. Transcription products of such nucleic acids are less likely, for example, to form hairpins than transcription products which contain all four nucleotides commonly found in RNA.
The Xs in the tetracysteine sequence may be any amino acids and may be the same or different. Examples of dipeptides which may be positioned between the two sets of cysteine residues include the following: (1) Pro-Gly, (2) Gly-Gly, (3) Ala-Gly, (4) Gly-Pro, (5) Ser-Gly, (6) Pro-Pro, (7) Ala-Ser, (8) Ser-Ser, (9) Trp-Gly, (10) Pro-Trp, (11) Phe-Gly, etc.
Tag sequence of the invention include those which contain the sequence (N-terminus) Cys-Cys-X-X-Cys-Cys (C-terminus) but have one or more amino acids associated with (1) their N-terminus, (2) their C-terminus, or (3) both their N-terminus and C-terminus. These amino acid at either the N-terminus, the C-terminus, or both termini may be designed to confer one or more particular conformations (e.g., random coil, beta-sheet, alpha helix, etc.) upon the tetracysteine sequence, when the tag is present either alone or bound to another amino acid sequence (e.g., when the tag is one component of a fusion protein). Examples of peptides which may be located at either the N-terminus, the C-terminus, or both termini of the tag include the following: (1) Ala-Gly-Gly, (2) Gly-Ala-Gly, (3) Gly-Ala-Ala, (4) Ala-Ala-Gly, (5) Ala-Ala-Ala, (6) Ser-Gly-Gly, (7) Gly-Ser-Gly, (8) Gly-Gly-Ser, (9) Ser-Ser-Gly, (10) Gly-Gly-Gly-Gly, (11) Gly-Pro-Ser, (12) and Gly-Gly-Gly-Gly-Ser, etc.
The tag may be located at either the N-terminus or the C-terminus, or located internally. When internally located, the tag may be positioned between different portions of the same protein or may contain all of part of two different proteins at both the N-terminus and the C-terminus of the tag. In other words, an internally located tag may have the following primary amino acid structure:
Protein A1-Gly-Gly-Cys-Cys-Pro-Gly-Cys-Cys-Gly-Gly-Protein A2 (SEQ ID NO:68), with “Protein A1” being the N-terminus of a protein and “Protein A2” being the C-terminus of the same protein and with the underlined amino sequence being the tag. This tag need not be one which binds to biarsenical compounds and includes other tags described herein (e.g., polypeptides which have one or more activities associated with β-lactamases).
The invention further includes methods for detecting molecules (e.g., tagged proteins) bound to solid supports. Thus, in one aspect the invention includes contacting and/or binding a tagged molecule to a solid support and detecting that molecule on the solid support. The detection methods employed may be essentially non-quantitative, semi-quantitative, or quantitative. In other words, the detection methods employed may (1) merely indicate that the tagged molecule is present, (2) provide a basis for roughly estimating the amount of tagged molecule present, or (3) provide a reasonably good measure of the amount of tagged molecules present (e.g., +/−5%). These detection methods may be, for example, colorimetric or fluorescence based.
In particular embodiments, tagged polypeptides are bound to a solid support, after which the presence of the tag is detected. One example of a method of the invention involves connecting a first nucleic acid molecules with a second nucleic acid molecule, wherein (1) the first nucleic acid molecule (e.g., a vector) encodes a polypeptide tag (e.g., a polypeptide comprising the sequence Cys-Cys-X-X-Cys-Cys, referred to herein as a tetracysteine sequence) and the second nucleic acid molecule encodes another amino acid sequence and (2) the two nucleic acid molecules are connected such that the polypeptide tag and the other amino acid sequence are encoded in-frame as a fusion product. The fusion product is then expressed and contacted with a solid support, after which the presence of the tag is detected.
When tags and/or tagged proteins are detected on a solid support, the tags and/or tagged proteins may be contacted with one or more detection reagents prior to the time that the tag and/or tagged protein are contacted with the support or afterward. Using as an example the detection of a protein tagged with a peptide that binds one or more biarsenical compounds after the tagged protein has been subjected to gel electrophoresis and then contacted with a solid support which is in the form of a membrane (e.g., a PVDF membrane), the tagged protein may be contacted with the detection reagent(s) prior to the gel electrophoresis step, during gel electrophoresis (e.g., the detection reagent(s) may be in the gel), after gel electrophoresis is complete (e.g., while the tagged protein is in the gel but before the gel and/or tagged protein are contacted with the solid support), and/or after the tagged protein has been contacted with and/or binds to the solid support.
Solid supports which may be used in the practice of the invention include beads (e.g., silica gel, controlled pore glass, magnetic, Sephadex/Sepharose, cellulose), flat surfaces or chips (e.g., glass fiber filters, glass surfaces, metal surface (steel, gold, silver, aluminum, copper and silicon), capillaries, plastic (e.g., polyethylene, polypropylene, polyamide, polyvinylidenedifluoride membranes or microtiter plates); or pins or combs made from similar materials comprising beads or flat surfaces or beads placed into pits in flat surfaces such as wafers (e.g., silicon wafers). Examples of solid supports also include acrylic, styrene-methyl methacrylate copolymers, ethylene/acrylic acid, acrylonitrile-butadiene-styrene (ABS), ABS/polycarbonate, ABS/polysulfone, ABS/polyvinyl chloride, ethylene propylene, ethylene vinyl acetate (EVA), nitrocellulose, nylons (including nylon 6, nylon 6/6, nylon 6/6-6, nylon 6/9, nylon 6/10, nylon 6/12, nylon 11 and nylon 12), polycarylonitrile (PAN), polyacrylate, polycarbonate, polybutylene terephthalate (PBT), polyethylene terephthalate (PET), polyethylene (including low density, linear low density, high density, cross-linked and ultra-high molecular weight grades), polypropylene homopolymer, polypropylene copolymers, polystyrene (including general purpose and high impact grades), polytetrafluoroethylene (PTFE), fluorinated ethylene-propylene (FEP), ethylene-tetrafluoroethylene (ETFE), perfluoroalkoxyethylene (PFA), polyvinyl fluoride (PVA), polyvinylidene fluoride (PVDF), polychlorotrifluoroethylene (PCTFE), polyethylene-chlorotrifluoroethylene (ECTFE), polyvinyl alcohol (PVA), silicon styrene-acrylonitrile (SAN), styrene maleic anhydride (SMA), metal oxides, and glass.
Biarsenical compounds suitable for use with tetracysteine tags of the invention include F
F
When tetracysteine amino acid sequence having affinity for a biarsenical compound is employed in methods of the invention (e.g., to bind the protein which contain the tetracysteine amino acid sequence to a biarsenical compound), proteins which contains the tetracysteine amino acid sequence may be contacted with the biarsenical compound in the presence of a reducing agent. Exemplary reducing agents include dithiothreitol (DTT), beta-mercaptoethanol (BME), Tris(2-carboxyethyl) phosphine HCl (TCEP), 1,2-ethanedithiol (EDT), 2,3-dimercapto-1-propanesulfonic acid (DMPS), and meso-2,3-dimercaptosuccinic acid (DMSA), tri-n-butylphosphine (TBP), 2-mercaptoethanol (2-ME or β-ME), and mercaptoethanesulfonic acid (MES), and combinations thereof.
When a reducing reagent is included in compositions used to practice methods of the invention it may be present in any suitable concentration, for example, 0.1 mM, 0.5 mM, 0.75 mM, 1 mM, 1.5 mM, 2 mM, 3 mM, 5 mM, 7.5 mM, 10 mM, etc. Suitable reducing reagent concentrations for particular applications may be determined by performing methods of the invention without and reducing agents present, followed by analysis of results obtained. Suitable reducing reagent concentrations for particular applications may also be determined by performing methods of the invention with reducing reagents present at different concentrations, followed by analysis of results obtained.
Methods employing reducing reagents are set out in U.S. Application No. 60/515,575, filed Oct. 28, 2003, the entire disclosure of which is incorporated herein by reference. U.S. Application No. 60/515,575 is directed, in part to the reduction of spurious binding of biarsenical fluorophores to vicinal cysteines of endogenous proteins by using mono- and dithiols to compete with the binding reaction. In many instances, reagents used in methods described in this application will be employed such that the competition does not substantially hinder the desired binding of the fluorophore to a tetracysteine tag.
Methods of the invention include those which involve double labeling or dual labeling of cells with at least two biarsenical compounds (e.g., F
When performing dual labeling methods, typically, the labels will be added at different times. For example, F
When in vivo labeling of cells is employed, it will often be advantageous to add one or more compounds to the cell solution which absorb background light. One example of such a compound is Disperse Blue 3. The use of this compound in conjunction with in vivo labeling is discussed below in Example 9.
One example of a method which may be used to label cells which express a protein with a suitable tetracysteine motif with F
One example of a method which may be used for in-gel detection of proteins) which contain a suitable tetracysteine motif with F
In particular embodiments, tagged proteins will contain two tags. One of these tags may be used, for example, for immobilizing the protein and the other for detection. In one specific example proteins of the invention contain an affinity tag such as a tag which binds to a metal chelate affinity chromatography matrix (e.g., a 6 His sequence) and another tag (e.g., a tag which binds to a biarsenical compound). The tag which binds to a metal chelate affinity chromatography matrix may be used to immobilize the protein and the other tag may then be used for detection.
In many instances, solid supports will be of a type which will bind a tagged molecule through a process which is not specific for the tag itself. In other words, in many instances, the tag will be left free to react with reagents used for detection (e.g., biarsenical compounds, fluorescent substrates such as CCF2 or CCF4, etc.), when it is necessary to employ such reagents. One example of such a binding process is the attachment of a tagged protein to a nitrocellulose membrane.
In one aspect, tagged molecules are separated from other molecules in a mixture by gel electrophoresis, followed by transfer to a solid support, such as a membrane (e.g., a PVDF membrane or a nitrocellulose membrane). The tagged molecules (e.g., tagged proteins) are then exposed to an agent which renders them detectable (e.g., a biarsenical), if necessary, and then detected. In many instances, detection will occur while the tagged molecule remains associated with the membrane.
In another aspect, tagged molecules are applied to the solid support in admixture with others molecules. For example, when the tagged molecule is a protein, a cell extract or a mixture comprising in vitro transcription/translation system components, for examples, may be applied directly to a solid support. Detection of the tag may then be employed to determine whether the tagged protein is present and, if so, how much of the tagged protein is present. In such a situation, a solution containing the tagged protein may be spotted onto the solid support in a defined region. Solutions containing other samples and/or one or more standards may, optionally, be spotted at other locations on the same or a different solid support. The tagged protein in the solution may be quantified, for example, by comparing the amount of detectable signal to the detectable signal generated by at least one standard.
One example of a method described above is set out below in Example 8, which led to the results shown in
The invention further includes nucleic acid molecules which encode fusion peptides which result from the connection of (1), (2), and/or (3), wherein (1) is a polypeptide encoded by a nucleic acid of interest, (2) is a peptide or polypeptide encoded by all or part of cloning site, and (3) a polypeptide having a detectable activity, as well as fusion proteins encoded by such nucleic acid molecules. Thus, the invention includes, for example, a fusion protein which contains one, two, three, four, five, six, seven, eight, nine, ten, etc. amino acid which are encoded for by (1), (2), and/or (3). As an example, the invention includes nucleic acid molecules wherein (2) is polypeptide or peptide encoded by a recombination sites (e.g., an attB 1 site, an attB2 site, etc.) and (3) is all or part of a β-lactamase polypeptide (e.g., a polypeptide with a β-lactamase activity, such as the ability to cleave a β-lactam ring). In such an instance, the fusion protein encoded by the nucleic acid molecule may comprise (1) one, two, three, four five, six, seven, eight, etc. amino acids encoded by an attB1 site and (2) all or part of a β-lactamase polypeptide. In particular instances, the amino acids of the fusion protein which are encoded by the attB1 site, or other recombination site, may be Pro-Ala-Phe-Leu-Tyr-Lys-Val-Val (SEQ ID NO:69), Ala-Phe-Leu-Tyr-Lys-Val-Val (SEQ ID NO:70), Phe-Leu-Tyr-Lys-Val-Val (SEQ ID NO:71), Leu-Tyr-Lys-Val-Val (SEQ ID NO:72), Tyr-Lys-Val-Val, Lys-Val-Val, Val-Val, Pro-Ala-Phe- or Val. Fusion proteins of the invention also include fusion proteins comprising an amino acid sequence encoded by any one of the recombination sites in Table 4 in any reading frame.
As noted above, the fusion protein may also comprise all or part of a β-lactamase. Furthermore, fusion proteins of the invention may comprise one, two, three, four, five, six, seven, eight, etc. amino acid encoded by a cloning sites (e.g., a recombination site) and all or part of the β-lactamase amino acid sequence shown in
In a specific embodiment of the invention, nucleic acid molecules of the invention may comprise a nucleic acid sequence encoding a polypeptide having an enzymatic activity (e.g., β-lactamase activity). In some embodiments, nucleic acid molecules of the invention may comprise nucleic acid sequence encoding a polypeptide having a detectable β-lactamase activity. Assays for β-lactamase activity are known in the art. U.S. Pat. Nos. 5,955,604, issued to Tsien, et al. Sep. 21, 1999, 5,741,657 issued to Tsien, et al., Apr. 21, 1998, 6,031,094, issued to Tsien, et al., Feb. 29, 2000, 6,291,162, issued to Tsien, et al., Sep. 18, 2001, and 6,472,205, issued to Tsien, et al. Oct. 29, 2002, disclose the use of β-lactamase as a reporter gene and fluorogenic substrates for use in detecting β-lactamase activity and are specifically incorporated herein by reference. In one embodiment of the invention, a nucleic acid sequence encoding a polypeptide having a detectable activity may be a nucleic acid sequence encoding a polypeptide having β-lactamase activity and desired host cells may be identified by assaying the host cells for β-lactamase activity.
A β-lactamase catalyzes the hydrolysis of a β-lactam ring. Those skilled in the art will appreciate that the sequences of a number of polypeptides having β-lactamase activity are known. In addition to the specific β-lactamases disclosed in the Tsien, et al. patents listed above, any polypeptide having β-lactamase activity is suitable for use in the present invention.
β-lactamases are classified based on amino acid and nucleotide sequence (Ambler, R. P., Phil. Trans. R. Soc. Lond. [Ser.B.] 289: 321-331 (1980)) into classes A-D. Class A β-lactamases possess a serine in the active site and have an approximate weight of 29 kd. This class contains the plasmid-mediated TEM β-lactamases such as the RTEM enzyme of pBR322. Class B β-lactamases have an active-site zinc bound to a cysteine residue. Class C enzymes have an active site serine and a molecular weight of approximately 39 kd, but have no amino acid homology to the class A enzymes. Class D enzymes also contain an active site serine. Representative examples of each class are provided below with the accession number at which the sequence of the enzyme may be obtained in the indicated database. The sequences of the enzymes in the following lists are specifically incorporated herein by reference.
Bacteroides fragilis CS30
Bacteroides uniformis WAL-7088
Bacteroides vulgatus CLA341
Proteus mirabilis GN179
Rhodopseudomonas capsulatus SP108
K. oxytoca E23004/SL781/SL7811
S. typhimurium CAS-5
Serratia fonticola CUV
Citrobacter diversus ULA27
Proteus vulgaris 5E78-1
Burkholderia cepacia 249
Yersinia enterocolitica serotype O:3/Y-56
M. tuberculosis H37RV
S. clavuligerus NRRL 3585
B. licheniformis 749/C
B. subtilis 168/6GM
Streptomyces badius DSM40139
Actinomadura sp. strain R39
Nocardia lactamdurans LC411
S. cacaoi KCC S0352
Streptomyces fradiae DSM40063
Streptomyces lavendulae DSM2014
Streptomyces albus G
S. lavendulae KCCS0263
Streptomyces aureofaciens
Streptomyces cellulosae KCCS0127
Mycobacterium fortuitum
S. aureus PC1/SK456/NCTC9789
Chryseobacterium meningosepticum
B. fragilis TAL3636/TAL2480
Aeromonas hydrophila AE036
Citrobacter freundii OS60/GN346
E. coli K-12/MG1655
Y. enterocolitica IP97/serotype O:5B
Morganella morganii SLM01
A. sobria 163a
K. pneumoniae NU2936
P. aeruginosa PAO1
S. marcescens SR50
Psychrobacter immobilis A5
Aeromonas sobria AER 14
Those skilled in the art will appreciate that any of the β-lactamase For additional β-lactamases and a more detailed description of substrate specificities, consult Bush et (1995) Antimicrob. Agents Chemother. 39:1211-1233. Those skilled in the art will appreciate that the polypeptides having β-lactamase activity disclosed herein may be altered by for example, mutating, deleting, and/or adding one or more amino acids and may still be used in the practice of the invention so long as the polypeptide retains detectable β-lactamase activity. An example of a suitably altered polypeptide having β-lactamase activity is one from which a signal peptide sequence has been deleted and/or altered such that the polypeptide is retained in the cytosol of prokaryotic and/or eukaryotic cells. The amino acid sequence of one such polypeptide is provided in Table 2.
One skilled in the art will appreciate that the sequence in Table 2 may be modified and still be within the scope of the present invention. For example, with reference to
As described in the above-referenced United States patents, host cells to be assayed may be contacted with a fluorogenic substrate for β-lactamase activity. In the presence of β-lactamase, the substrate is cleaved and the fluorescence emission spectrum of the substrate is altered. As an example, un-cleaved substrate may fluoresce green (i.e., have an emission maxima at approximately 520 nm) when excited with light having a wavelength of 405 nm and the cleaved substrate may fluoresce blue (i.e., have an emission maxima at approximately 447 nm). By determining the ratio of green fluorescence intensity to blue fluorescence intensity it is possible to determine the amount of β-lactamase produced and from that, to calculate what % of the cells express β-lactamase. Kits for conducting a fluorescence-based β-lactamase assay are commercially available, for example, from PanVera, LLC, Madison, Wis., catalog number K1032 now owned by Invitrogen Corporation, Carlsbad, Calif.
β-lactam fluorogenic substrates for use in the present invention include those which comprise a fluorescence donor moiety and a fluorescence acceptor moiety linked to a cephalosporin backbone such that, upon hydrolysis of the β-lactam, the acceptor moiety is released from the molecule. Before the β-lactam is hydrolyzed, the donor and acceptor moiety are positioned such that efficient fluorescence resonance energy transfer (FRET) occurs. Upon excitation with light of a suitable wavelength, fluorescence from the acceptor moiety is observed. After hydrolysis of the β-lactam, the acceptor moiety is released from the molecule and the FRET is disrupted resulting in a change in the fluorescence emission spectrum. An example of a suitable fluorescence donor molecule is a coumarin or derivative thereof (e.g., 6-chloro-7-hydroxycoumarin) and examples of suitable acceptor moieties include, but are not limited to, fluoresceine, rhodol, or rhodamine or derivatives thereof. Examples of suitable substrates include CCF2 and the acetoxymethyl ester derivative thereof (CCF2/AM) and CCF4 and the acetoxymethyl ester derivative thereof (CCF4/AM). Those skilled in the art will appreciate that the ester derivatives are membrane permeable and are de-esterified inside a cell by the action of endogenous esterase enzymes. The structures of CCF2 and CCF4 are provided in
In some embodiments, nucleic acid molecules comprising a nucleic acid sequence encoding a polypeptide having a detectable activity may encode a polypeptide having the ability to bind to specific molecules or classes of molecules. In one embodiment, polypeptides having a detectable activity may have the ability to molecules comprising one or more arsenic atoms. One non-limiting example of a polypeptide having the ability to bind molecules comprising one or more arsenic atoms is -Ala-Gly-Gly-Cys-Cys-Pro-Gly-Cys-Cys-Gly-Gly-Gly-(SEQ ID NO:78). This polypeptide sequence may be placed at any position in a fusion protein comprising it, for example, at the N-terminus, at one or more internal positions, and/or at the C-terminus. The present invention also encompasses derivatives of this polypeptide, for example, one or more of the non-cysteine amino acids may be substituted. Polypeptides of this type may bind to molecules comprising one or more arsenic atoms (see, for example, U.S. Pat. Nos. 5,932,474, 6,008,378, 6,054,271, and 6,451,569 and published international patent application WO 01/53325A2). Upon binding of the polypeptides to the molecules comprising one or more arsenic atoms, the molecules may undergo a change in spectral properties (e.g., fluorescent properties). For example, upon binding of a polypeptides, the molecules comprising one or more arsenic atoms may become fluorescent.
Recombination sites for use in the invention may be any nucleic acid that can serve as a substrate in a recombination reaction. Such recombination sites may be wild-type or naturally occurring recombination sites, or modified, variant, derivative, or mutant recombination sites. Examples of recombination sites for use in the invention include, but are not limited to, phage-lambda recombination sites (such as attP, attB, attL, and attR and mutants or derivatives thereof) and recombination sites from other bacteriophages such as phi80, P22, P2, 186, P4 and P1 (including lox sites such as loxP and loxP511).
Recombination proteins and mutant, modified, variant, or derivative recombination sites for use in the invention include those described in U.S. Pat. Nos. 5,888,732, 6,143,557, 6,171,861, 6,270,969, and 6,277,608 and in U.S. application Ser. No. 09/438,358, filed Nov. 12, 1999, which are specifically incorporated herein by reference. Mutated att sites (e.g., attB 1-10, attP 1-10, attR 1-10 and attL 1-10) are described in U.S. application Ser. No. 09/517,466, filed Mar. 2, 2000, and 09/732,914, filed Dec. 11, 2000 (published as US 2002/0007051-A1) the disclosures of which are specifically incorporated herein by reference in their entirety. Other suitable recombination sites and proteins are those associated with the G
Recombination sites that may be used in the present invention include att sites. The 15 bp core region of the wild-type att site (GCTTTTTTAT ACTAA (SEQ ID NO:79)), which is identical in all wild-type att sites, may be mutated in one or more positions. Engineered att sites that specifically recombine with other engineered att sites can be constructed by altering nucleotides in and near the 7 base pair overlap region, bases 6-12, of the core region. Thus, recombination sites suitable for use in the methods, molecules, compositions, and vectors of the invention include, but are not limited to, those with insertions, deletions or substitutions of one, two, three, four, or more nucleotide bases within the 15 base pair core region (see U.S. Pat. Nos. 5,888,732 and 6,277,608, which describe the core region in further detail, and the disclosures of which are incorporated herein by reference in their entireties). Recombination sites suitable for use in the methods, compositions, and vectors of the invention also include those with insertions, deletions or substitutions of one, two, three, four, or more nucleotide bases within the 15 base pair core region that are at least 50% identical, at least 55% identical, at least 60% identical, at least 65% identical, at least 70% identical, at least 75% identical, at least 80% identical, at least 85% identical, at least 90% identical, or at least 95% identical to this 15 base pair core region.
As a practical matter, whether any particular nucleic acid molecule is at least 50%, 60%, 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% identical to, for instance, a given recombination site nucleotide sequence or portion thereof can be determined conventionally using known computer programs such as DNAsis software (Hitachi Software, San Bruno, California) for initial sequence alignment followed by ESEE version 3.0 DNA/protein sequence software (cabot@trog.mbb.sfu.ca) for multiple sequence alignments. Alternatively, such determinations may be accomplished using the BESTFIT program (Wisconsin Sequence Analysis Package, Genetics Computer Group, University Research Park, 575 Science Drive, Madison, Wis. 53711), which employs a local homology algorithm (Smith and Waterman, Advances in Applied Mathematics 2: 482-489 (1981)) to find the best segment of homology between two sequences. When using DNAsis, ESEE, BESTFIT or any other sequence alignment program to determine whether a particular sequence is, for instance, 95% identical to a reference sequence according to the present invention, the parameters are set such that the percentage of identity is calculated over the full length of the reference nucleotide sequence and that gaps in homology of up to 5% of the total number of nucleotides in the reference sequence are allowed. Computer programs such as those discussed above may also be used to determine percent identity and homology between two proteins at the amino acid level.
Analogously, the core regions in attB1, attP1, attL1 and attR1 are identical to one another, as are the core regions in attB2, attP2, attL2 and attR2. Nucleic acid molecules suitable for use with the invention also include those comprising insertions, deletions or substitutions of one, two, three, four, or more nucleotides within the seven base pair overlap region (TTTATAC, bases 6-12 in the core region). The overlap region is defined by the cut sites for the integrase protein and is the region where strand exchange takes place. Examples of such mutants, fragments, variants and derivatives include, but are not limited to, nucleic acid molecules in which (1) the thymine at position 1 of the seven by overlap region has been deleted or substituted with a guanine, cytosine, or adenine; (2) the thymine at position 2 of the seven by overlap region has been deleted or substituted with a guanine, cytosine, or adenine; (3) the thymine at position 3 of the seven by overlap region has been deleted or substituted with a guanine, cytosine, or adenine; (4) the adenine at position 4 of the seven by overlap region has been deleted or substituted with a guanine, cytosine, or thymine; (5) the thymine at position 5 of the seven by overlap region has been deleted or substituted with a guanine, cytosine, or adenine; (6) the adenine at position 6 of the seven by overlap region has been deleted or substituted with a guanine, cytosine, or thymine; and (7) the cytosine at position 7 of the seven by overlap region has been deleted or substituted with a guanine, thymine, or adenine; or any combination of one or more (e.g., two, three, four, five, etc.) such deletions and/or substitutions within this seven by overlap region. The nucleotide sequences of representative seven base pair core regions are set out below.
Altered att sites have been constructed that demonstrate that (1) substitutions made within the first three positions of the seven base pair overlap (TTTATAC) strongly affect the specificity of recombination, (2) substitutions made in the last four positions (TTTATAC) only partially alter recombination specificity, and (3) nucleotide substitutions outside of the seven by overlap, but elsewhere within the 15 base pair core region, do not affect specificity of recombination but do influence the efficiency of recombination. Thus, nucleic acid molecules and methods of the invention include those comprising or employing one, two, three, four, five, six, eight, ten, or more recombination sites which affect recombination specificity, particularly one or more (e.g., one, two, three, four, five, six, eight, ten, twenty, thirty, forty, fifty, etc.) different recombination sites that may correspond substantially to the seven base pair overlap within the 15 base pair core region, having one or more mutations that affect recombination specificity. Such molecules may comprise a consensus sequence such as NNNATAC wherein “N” refers to any nucleotide (i.e., may be A, G, T/U or C, or an analogue or derivative thereof). In particular embodiments, if one of the first three nucleotides in the consensus sequence is a T/U, then at least one of the other two of the first three nucleotides is not a T/U.
The core sequence of each att site (attB, attP, attL and attR) can be divided into functional units consisting of integrase binding sites, integrase cleavage sites and sequences that determine specificity. Specificity determinants are defined by the first three positions following the integrase top strand cleavage site. These three positions are shown with underlining in the following reference sequence: CAACTTTTTTATAC AAAGTTG (SEQ ID NO:80). Modification of these three positions (64 possible combinations) can be used to generate att sites that recombine with high specificity with other att sites having the same sequence for the first three nucleotides of the seven base pair overlap region. The possible combinations of first three nucleotides of the overlap region are shown in Table 3.
Representative examples of seven base pair att site overlap regions suitable for use in methods, compositions and vectors of the invention are shown in Table 4. The invention further includes nucleic acid molecules comprising one or more (e.g., one, two, three, four, five, six, eight, ten, twenty, thirty, forty, fifty, etc.) nucleotides sequences set out in Table 2. Thus, for example, in one aspect, the invention provides nucleic acid molecules comprising the nucleotide sequence GAAATAC, GATATAC, ACAATAC, or TGCATAC.
As noted above, alterations of nucleotides located 3′ to the three base pair region discussed above can also affect recombination specificity. For example, alterations within the last four positions of the seven base pair overlap can also affect recombination specificity.
For example, mutated att sites that may be used in the practice of the present invention include attB1 (AGCCTGCTTT TTTGTACAAA CTTGT (SEQ ID NO:81)), attP1 (TACAGGTCAC TAATACCATC TAAGTAGTTG ATTCATAGTG ACTGGATATG TTGTGTTTTA CAGTATTATG TAGTCTGTTT TTTATGCAAA ATCTAATTTA ATATATTGAT ATTTATATCA TTTTACGTTT CTCGTTCAGC TTTTTTGTAC AAAGTTGGCA TTATAAAAAA GCATTGCTCA TCAATTTGTT GCAACGAACA GGTCACTATC AGTCAAAATA AAATCATTAT TTG (SEQ ID NO:82)), attL1 (CAAATAATGA TTTTATTTTG ACTGATAGTG ACCTGTTCGT TGCAACAAAT TGATAAGCAA TGCTTTTTTA TAATGCCAAC TTTGTACAAA AAAGCAGGCT (SEQ ID NO:83)), and attR1 (ACAAGTTTGT ACAAAAAAGC TGAACGAGAA ACGTAAAATG ATATAAATAT CAATATATTA AATTAGATTT TGCATAAAAA ACAGACTACA TAATACTGTA AAACACAACA TATCCAGTCA CTATG (SEQ ID NO:84)). Table 5 provides the sequences of the regions surrounding the core region for the wild type att sites (attB0, P0, R0, and L0) as well as a variety of other suitable recombination sites. Those skilled in the art will appreciated that the remainder of the site may be the same as the corresponding site (B, P, L, or R) listed above.
Other recombination sites having unique specificity (i.e., a first site will recombine with its corresponding site and will not substantially recombine with a second site having a different specificity) are known to those skilled in the art and may be used to practice the present invention. Corresponding recombination proteins for these systems may be used in accordance with the invention with the indicated recombination sites. Other systems providing recombination sites and recombination proteins for use in the invention include the FLP/FRT system from Saccharomyces cerevisiae, the resolvase family (e.g., γδ, TndX, TnpX, Tn3 resolvase, Hin, Hjc, Gin, SpCCE1, ParA, and Cin), and IS231 and other Bacillus thuringiensis transposable elements. Other suitable recombination systems for use in the present invention include the XerC and XerD recombinases and the psi, dif and cer recombination sites in E. coli. Other suitable recombination sites may be found in U.S. Pat. No. 5,851,808 issued to Elledge and Liu which is specifically incorporated herein by reference.
Those skilled in the art can readily optimize the conditions for conducting the recombination reactions described herein without the use of undue experimentation, based on the guidance provided herein and available in the art (see, e.g., U.S. Pat. Nos. 5,888,732 and 6,277,608, which are specifically incorporated herein by reference in their entireties). In a typical reaction from, about 50 ng to about 1000 ng of a second nucleic acid molecule may be contacted with a first nucleic acid molecule under suitable reaction conditions. Each nucleic acid molecule may be present in a molar ratio of from about 25:1 to about 1:25 first nucleic acid molecule:second nucleic acid molecule. In some embodiments, a first nucleic acid molecule may be present at a molar ratio of from about 10:1 to 1:10 first nucleic acid molecule:second nucleic acid molecule. In one embodiment, each nucleic acid molecule may be present at a molar ratio of about 1:1 first nucleic acid molecule:second nucleic acid molecule.
Typically, the nucleic acid molecules may be dissolved in an aqueous buffer and added to the reaction mixture. One suitable set of conditions is 4 μl C
Proteins for conducting an LR reaction may be stored in a suitable buffer, for example, LR Storage Buffer, which may comprise about 50 mM Tris at about pH 7.5, about 50 mM NaCl, about 0.25 mM EDTA, about 2.5 mM Spermidine, and about 0.2 mg/ml BSA. When stored, proteins for an LR reaction may be stored at a concentration of about 37.5 ng/μl INT, 10 ng/μl IHF and 15 ng/μl XIS. Proteins for conducting a BP reaction may be stored in a suitable buffer, for example, BP Storage Buffer, which may comprise about 25 mM Tris at about pH 7.5, about 22 mM NaCl, about 5 mM EDTA, about 5 mM Spermidine, about 1 mg/ml BSA, and about 0.0025% Triton X-100. When stored, proteins for an BP reaction may be stored at a concentration of about 37.5 ng/μl INT and 20 ng/μl IHF. One skilled in the art will recognize that enzymatic activity may vary in different preparations of enzymes. The amounts suggested above may be modified to adjust for the amount of activity in any specific preparation of enzymes.
A suitable 5× reaction buffer for conducting recombination reactions may comprise 100 mM Tris pH 7.5, 88 mM NaCl, 20 mM EDTA, 20 mM Spermidine, and 4 mg/ml BSA. Thus, in a recombination reaction, the final buffer concentrations may be 20 mM Tris pH 7.5, 17.6 mM NaCl, 4 mM EDTA, 4 mM Spermidine, and 0.8 mg/ml BSA. Those skilled in the art will appreciate that the final reaction mixture may incorporate additional components added with the reagents used to prepare the mixture, for example, a BP reaction may include 0.005% Triton X-100 incorporated from the BP C
In some embodiments, particularly those in which attL sites are to be recombined with attR sites, the final reaction mixture may include about 50 mM Tris HCl, pH 7.5, about 1 mM EDTA, about 1 mg/ml BSA, about 75 mM NaCl and about 7.5 mM spermidine in addition to recombination enzymes and the nucleic acids to be combined. In other embodiments, particularly those in which an attB site is to be recombined with an attP site, the final reaction mixture may include about 25 mM Tris HCl, pH 7.5, about 5 mM EDTA, about 1 mg/ml bovine serum albumin (BSA), about 22 mM NaCl, and about 5 mM spermidine.
In some embodiments, particularly those in which attL sites are to be recombined with attR sites, the final reaction mixture may include about 40 mM Tris HCl, pH 7.5, about 1 mM EDTA, about 1 mg/ml BSA, about 64 mM NaCl and about 8 mM spermidine in addition to recombination enzymes and the nucleic acids to be combined. One of skill in the art will appreciate that the reaction conditions may be varied somewhat without departing from the invention. For example, the pH of the reaction may be varied from about 7.0 to about 8.0; the concentration of buffer may be varied from about 25 mM to about 100 mM; the concentration of EDTA may be varied from about 0.5 mM to about 2 mM; the concentration of NaCl may be varied from about 25 mM to about 150 mM; and the concentration of BSA may be varied from 0.5 mg/ml to about 5 mg/ml. In other embodiments, particularly those in which an attB site is to be recombined with an attP site, the final reaction mixture may include about 25 mM Tris HCl, pH 7.5, about 5 mM EDTA, about 1 mg/ml bovine serum albumin (BSA), about 22 mM NaCl, about 5 mM spermidine and about 0.005% detergent (e.g., Triton X-100).
The present invention also relates to methods of using one or more topoisomerases to generate a recombinant nucleic acid molecules of the invention (e.g., molecules comprising one or more nucleic acid sequence encoding a polypeptide having a detectable activity) comprising two or more nucleotide sequences, any one or more of which may comprise, for example, all or a portion of a nucleic acid sequence encoding a polypeptide having a detectable activity. Topoisomerases may be used in combination with recombinational cloning techniques described above. For example, a topoisomerase-mediated reaction may be used to attach one or more recombination sites to one or more nucleic acid segments. The segments may then be further manipulated and combined using, for example, recombinational cloning techniques.
In one aspect, the present invention provides methods for linking a first and at least a second nucleic acid segment (either or both of which may contain one or more nucleic acid sequences encoding a polypeptide having a detectable activity and/or sequences of interest) with at least one (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, etc.) topoisomerase (e.g., a type IA, type IB, and/or type II topoisomerase) such that either one or both strands of the linked segments are covalently joined at the site where the segments are linked.
A method for generating a double stranded recombinant nucleic acid molecule covalently linked in one strand can be performed by contacting a first nucleic acid molecule which has a site-specific topoisomerase recognition site (e.g., a type IA or a type II topoisomerase recognition site), or a cleavage product thereof, at a 5′ or 3′ terminus, with a second (or other) nucleic acid molecule, and optionally, a topoisomerase (e.g., a type IA, type IB, and/or type II topoisomerase), such that the second nucleotide sequence can be covalently attached to the first nucleotide sequence. As disclosed herein, the methods of the invention can be performed using any number of nucleotide sequences, typically nucleic acid molecules wherein at least one of the nucleotide sequences has a site-specific topoisomerase recognition site (e.g., a type IA, type IB or type II topoisomerase), or cleavage product thereof, at one or both 5′ and/or 3′ termini.
In some embodiments, two double-stranded nucleic acid molecules can be joined into a one larger molecule such that each strand of the larger molecule is covalently joined (e.g., the larger molecule has no nicks). With reference to
In another embodiment, a first nucleic acid molecule having a topoisomerase bound to the 3′ terminus of one end, and a second nucleic acid molecule having a topoisomerase bound to the 3′ terminus of one end may be joined using the methods of the invention (
A method for generating a double stranded recombinant nucleic acid molecule covalently linked in both strands can be performed, for example, by contacting a first nucleic acid molecule having a first end and a second end, wherein, at the first end or second end or both ends, the first nucleic acid molecule has a topoisomerase recognition site (or cleavage product thereof) at or near the 5′ or 3′ terminus; at least a second nucleic acid molecule having a first end and a second end, wherein, at the first end or second end or both ends, the at least second double stranded nucleotide sequence has a topoisomerase recognition site (or cleavage product thereof) at or near a 5′ or 3′ terminus; and at least one site specific topoisomerase (e.g., a type IA and/or a type IB topoisomerase), under conditions such that all components are in contact and the topoisomerase can effect its activity. A covalently linked double stranded recombinant nucleic acid generated according to a method of this aspect of the invention is characterized, in part, in that it does not contain a nick in either strand at the position where the nucleic acid molecules are joined. In one embodiment, the method is performed by contacting a first nucleic acid molecule and a second (or other) nucleic acid molecule, each of which has a topoisomerase recognition site in addition to viral sequences an/or sequences of interest, or a cleavage product thereof, at the 3′ termini or at the 5′ termini of two ends to be covalently linked. In another embodiment, the method is performed by contacting a first nucleic acid molecule having a topoisomerase recognition site, or cleavage product thereof, at the 5′ terminus and the 3′ terminus of at least one end, and a second (or other) nucleic acid molecule having a 3′ hydroxyl group and a 5′ hydroxyl group at the end to be linked to the end of the first nucleic acid molecule containing the recognition sites. As disclosed herein, the methods can be performed using any number of nucleic acid molecules having various combinations of termini and ends.
Topoisomerases are categorized as type I, including type IA and type IB topoisomerases, which cleave a single strand of a double stranded nucleic acid molecule, and type II topoisomerases (gyrases), which cleave both strands of a nucleic acid molecule. Type IA and IB topoisomerases cleave one strand of a nucleic acid molecule. Cleavage of a nucleic acid molecule by type IA topoisomerases generates a 5′ phosphate and a 3′ hydroxyl at the cleavage site, with the type IA topoisomerase covalently binding to the 5′ terminus of a cleaved strand. In comparison, cleavage of a nucleic acid molecule by type IB topoisomerases generates a 3′ phosphate and a 5′ hydroxyl at the cleavage site, with the type IB topoisomerase covalently binding to the 3′ terminus of a cleaved strand. As disclosed herein, type I and type II topoisomerases, as well as catalytic domains and mutant forms thereof, are useful for generating double stranded recombinant nucleic acid molecules covalently linked in both strands according to a method of the invention.
Type IA topoisomerases include E. coli topoisomerase I, E. coli topoisomerase III, eukaryotic topoisomerase II, archeal reverse gyrase, yeast topoisomerase III, Drosophila topoisomerase III, human topoisomerase III, Streptococcus pneumoniae topoisomerase III, and the like, including other type IA topoisomerases (see Berger, Biochim. Biophys. Acta 1400:3-18, 1998; DiGate and Marians, J. Biol. Chem. 264:17924-17930, 1989; Kim and Wang, J. Biol. Chem. 267:17178-17185, 1992; Wilson, et al., J. Biol. Chem. 275:1533-1540, 2000; Hanai, et al., Proc. Natl. Acad. Sci., USA 93:3653-3657, 1996, U.S. Pat. No. 6,277,620, each of which is incorporated herein by reference). E. coli topoisomerase III, which is a type IA topoisomerase that recognizes, binds to and cleaves the sequence 5′-GCAACTT-3′, can be particularly useful in a method of the invention (Zhang, et al., J. Biol. Chem. 270:23700-23705, 1995, which is incorporated herein by reference). A homolog, the traE protein of plasmid RP4, has been described by Li, et al., J. Biol. Chem. 272:19582-19587 (1997) and can also be used in the practice of the invention. A DNA-protein adduct is formed with the enzyme covalently binding to the 5′-thymidine residue, with cleavage occurring between the two thymidine residues.
Type D3 topoisomerases include the nuclear type I topoisomerases present in all eukaryotic cells and those encoded by vaccinia and other cellular poxviruses (see Cheng, et al., Cell 92:841-850, 1998, which is incorporated herein by reference). The eukaryotic type IB topoisomerases are exemplified by those expressed in yeast, Drosophila and mammalian cells, including human cells (see Caron and Wang, Adv. Pharmacol. 29B:271-297, 1994; Gupta, et al., Biochim. Biophys. Acta 1262:1-14, 1995, each of which is incorporated herein by reference; see, also, Berger, supra, 1998). Viral type IB topoisomerases are exemplified by those produced by the vertebrate poxviruses (vaccinia, Shope fibroma virus, ORF virus, fowlpox virus, and molluscum contagiosum virus), and the insect poxvirus (Amsacta moorei entomopoxvirus) (see Shuman, Biochim. Biophys. Acta 1400:321-337, 1998; Petersen, et al., Virology 230:197-206, 1997; Shuman and Prescott, Proc. Natl. Acad. Sci., USA 84:7478-7482, 1987; Shuman, J. Biol. Chem. 269:32678-32684, 1994; U.S. Pat. No. 5,766,891; PCT/US95/16099; PCT/US98/12372, each of which is incorporated herein by reference; see, also, Cheng, et al., supra, 1998).
Type II topoisomerases include, for example, bacterial gyrase, bacterial DNA topoisomerase IV, eukaryotic DNA topoisomerase II, and T-even phage encoded DNA topoisomerases (Roca and Wang, Cell 71:833-840, 1992; Wang, J. Biol. Chem. 266:6659-6662, 1991, each of which is incorporated herein by reference; Berger, supra, 1998). Like the type IB topoisomerases, the type II topoisomerases have both cleaving and ligating activities. In addition, like type IB topoisomerase, substrate nucleic acid molecules can be prepared such that the type II topoisomerase can form a covalent linkage to one strand at a cleavage site. For example, calf thymus type II topoisomerase can cleave a substrate nucleic acid molecule containing a 5′ recessed topoisomerase recognition site positioned three nucleotides from the 5′ end, resulting in dissociation of the three nucleotide sequence 5′ to the cleavage site and covalent binding the of the topoisomerase to the 5′ terminus of the nucleic acid molecule (Andersen, et al., supra, 1991). Furthermore, upon contacting such a type II topoisomerase charged nucleic acid molecule with a second nucleotide sequence containing a 3′ hydroxyl group, the type II topoisomerase can ligate the sequences together, and then is released from the recombinant nucleic acid molecule. As such, type II topoisomerases also are useful for performing methods of the invention.
The various topoisomerases exhibit a range of sequence specificity. For example, type II topoisomerases can bind to a variety of sequences, but cleave at a highly specific recognition site (see Andersen, et al., J. Biol. Chem. 266:9203-9210, 1991, which is incorporated herein by reference.). In comparison, the type IB topoisomerases include site specific topoisomerases, which bind to and cleave a specific nucleotide sequence (“topoisomerase recognition site”). Upon cleavage of a nucleic acid molecule by a topoisomerase, for example, a type IB topoisomerase, the energy of the phosphodiester bond is conserved via the formation of a phosphotyrosyl linkage between a specific tyrosine residue in the topoisomerase and the 3′ nucleotide of the topoisomerase recognition site. Where the topoisomerase cleavage site is near the 3′ terminus of the nucleic acid molecule, the downstream sequence (3′ to the cleavage site) can dissociate, leaving a nucleic acid molecule having the topoisomerase covalently bound to the newly generated 3′ end.
In particular embodiments, the 5′ termini of the ends of the nucleotide sequences to be linked by a type IB topoisomerase according to a method of certain aspects of the invention contain complementary 5′ overhanging sequences, which can facilitate the initial association of the nucleotide sequences, including, if desired, in a predetermined directional orientation. Alternatively, the 5′ termini of the ends of the nucleotide sequences to be linked by a type IB topoisomerase according to a method of certain aspects of the invention contain complementary 5′ sequences wherein one of the sequences contains a 5′ overhanging sequence and the other nucleotide sequence contains a complementary sequence at a blunt end of a 5′ terminus, to facilitate the initial association of the nucleotide sequences through strand invasion, including, if desired, in a predetermined directional orientation (
In particular embodiments, the 3′ termini of the ends of the nucleotide sequences to be linked by a type IA topoisomerase according to a method of certain aspects of the invention contain complementary 3′ overhanging sequences, which can facilitate the initial association of the nucleotide sequences, including, if desired, in a predetermined directional orientation. Alternatively, the 3′ termini of the ends of the nucleotide sequences to be linked by a topoisomerase (e.g., a type IA or a type II topoisomerase) according to a method of certain aspects of the invention contain complementary 3′ sequences wherein one of the sequences contains a 3′ overhanging sequence and the other nucleotide sequence contains a complementary sequence at a blunt end of a 3′ terminus, to facilitate the initial association of the nucleotide sequences through strand invasion, including, if desired, in a predetermined directional orientation. The term “3′ overhang” or “3′ overhanging sequence” is used herein to refer to a strand of a nucleic acid molecule that extends in a 3′ direction beyond the terminus of the complementary strand of the nucleic acid molecule. Conveniently, a 3′ overhang can be produced upon cleavage by a type IA or type II topoisomerase.
The 3′ or 5′ overhanging sequences can have any sequence, though generally the sequences are selected such that they allow ligation of a predetermined end of one nucleic acid molecule to a predetermined end of a second nucleotide sequence according to a method of the invention. As such, while the 3′ or 5′ overhangs can be palindromic, they generally are not because nucleic acid molecules having palindromic overhangs can associate with each other, thus reducing the yield of a ds recombinant nucleic acid molecule covalently linked in both strands comprising two or more nucleic acid molecules in a predetermined orientation.
Any number of methods may be used to add topoisomerase cleavage sites to nucleic acid molecules and/or generate nucleic acid molecules to which topoisomerase is covalently bound. Examples of such methods are set out below in Example 8 and in U.S. Patent Publication No. 2003-0186233, the entire disclosure of which is incorporated herein by reference.
Suppressor tRNAs
Mutant tRNA molecules that recognize what are ordinarily stop codons suppress the termination of translation of an mRNA molecule and are termed suppressor tRNAs. Three codons are used by both eukaryotes and prokaryotes to signal the end of gene. When transcribed into mRNA, the codons have the following sequences: UAG (amber), UGA (opal) and UAA (ochre). Under most circumstances, the cell does not contain any tRNA molecules that recognize these codons. Thus, when a ribosome translating an mRNA reaches one of these codons, the ribosome stalls and falls of the RNA, terminating translation of the mRNA. The release of the ribosome from the mRNA is mediated by specific factors (see S. Mottagui-Tabar, Nucleic Acids Research 26(11), 2789, 1998). A gene with an in-frame stop codon (TAA, TAG, or TGA) will ordinarily encode a protein with a native carboxy terminus. However, suppressor tRNAs can result in the insertion of amino acids and continuation of translation past stop codons.
A number of such suppressor tRNAs have been found. Examples include, but are not limited to, the supE, supP, supD, supF and supZ suppressors, which suppress the termination of translation of the amber stop codon, supB, glT, supL, supN, supC and supM suppressors, which suppress the function of the ochre stop codon and glyT, trpT and Su-9 suppressors, which suppress the function of the opal stop codon. In general, suppressor tRNAs contain one or more mutations in the anti-codon loop of the tRNA that allows the tRNA to base pair with a codon that ordinarily functions as a stop codon. The mutant tRNA is charged with its cognate amino acid residue and the cognate amino acid residue is inserted into the translating polypeptide when the stop codon is encountered. For a more detailed discussion of suppressor tRNAs, the reader may consult Eggertsson, et al., (1988) Microbiological Review 52(3):354-374, and Engleerg-Kukla, et al. (1996) in Escherichia coli and Salmonella Cellular and Molecular Biology, Chapter 60, pps 909-921, Neidhardt, et al. eds., ASM Press, Washington, D.C.
Mutations that enhance the efficiency of termination suppressors, i.e., increase the read through of the stop codon, have been identified. These include, but are not limited to, mutations in the uar gene (also known as the prfA gene), mutations in the ups gene, mutations in the sueA, sueB and sueC genes, mutations in the rpsD (ramA) and rpsE (spcA) genes and mutations in the rplL gene.
Under ordinary circumstances, host cells would not be expected to be healthy if suppression of stop codons is too efficient. This is because of the thousands or tens of thousands of genes in a genome, a significant fraction will naturally have one of the three stop codons; complete read-through of these would result in a large number of aberrant proteins containing additional amino acids at their carboxy termini. If some level of suppressing tRNA is present, there is a race between the incorporation of the amino acid and the release of the ribosome. Higher levels of tRNA may lead to more read-through although other factors, such as the codon context, can influence the efficiency of suppression.
Organisms ordinarily have multiple genes for tRNAs. Combined with the redundancy of the genetic code (multiple codons for many of the amino acids), mutation of one tRNA gene to a suppressor tRNA status does not lead to high levels of suppression. The TAA stop codon is the strongest, and most difficult to suppress. The TGA is the weakest, and naturally (in E. coli) leaks to the extent of 3%. The TAG (amber) codon is relatively tight, with a read-through of ˜1% without suppression. In addition, the amber codon can be suppressed with efficiencies on the order of 50% with naturally occurring suppressor mutants. Suppression in some organisms (e.g., E. coli) may be enhanced when the nucleotide following the stop codon is an adenosine. Thus, the present invention contemplates nucleic acid molecules having a stop codon followed by an adenosine (e.g., having the sequence TAGA, TAAA, and/or TGAA).
Suppression has been studied for decades in bacteria and bacteriophages. In addition, suppression is known in yeast, flies, plants and other eukaryotic cells including mammalian cells. For example, Capone, et al. (Molecular and Cellular Biology 6(9):3059-3067, 1986) demonstrated that suppressor tRNAs derived from mammalian tRNAs could be used to suppress a stop codon in mammalian cells. A copy of the E. coli chloramphenicol acetyltransferase (cat) gene having a stop codon in place of the codon for serine 27 was transfected into mammalian cells along with a gene encoding a human serine tRNA that had been mutated to form an amber, ochre, or opal suppressor derivative of the gene. Successful expression of the cat gene was observed. An inducible mammalian amber suppressor has been used to suppress a mutation in the replicase gene of polio virus and cell lines expressing the suppressor were successfully used to propagate the mutated virus (Sedivy, et al., Cell 50: 379-389 (1987)). The context effects on the efficiency of suppression of stop codons by suppressor tRNAs has been shown to be different in mammalian cells as compared to E. coli (Phillips-Jones, et al., Molecular and Cellular Biology 15(12): 6593-6600 (1995), Martin, et al., Biochemical Society Transactions 21: (1993)) Since some human diseases are caused by nonsense mutations in essential genes, the potential of suppression for gene therapy has long been recognized (see Temple, et al., Nature 296(5857):537-40 (1982)). The suppression of single and double nonsense mutations introduced into the diphtheria toxin A-gene has been used as the basis of a binary system for toxin gene therapy (Robinson, et al., Human Gene Therapy 6:137-143 (1995)).
Use of Suppressor tRNAs to Conditionally Express Fusion Proteins
Because the methods used to create the nucleic acids of the invention are site specific, the orientation and/or reading frame of a nucleic acid sequence on a first nucleic acid molecule can be controlled with respect to the orientation and/or reading frame of a sequence on a second nucleic acid molecule when all or a portion of the molecules are joined in a recombination and/or topoisomerase-mediated reaction. This control makes the construction of fusions between sequences present on different nucleic acid molecules a simple matter.
In general terms, an open reading frame may be expressed in four forms: native at both amino and carboxy termini, modified at either end, or modified at both ends. The portion of a nucleic acid sequence encoding a polypeptide of interest may be referred to as an open reading frame (ORF). A nucleic acid sequence of interest comprising an ORF of interest may include the N-terminal methionine ATG codon, and a stop codon at the carboxy end, of the ORF, thus ATG-ORF-stop. Frequently, the nucleic acid molecule comprising the sequence of interest will include translation initiation sequences, tis, that may be located upstream of the ATG that allow expression of the gene, thus tis-ATG-ORF-stop. Constructs of this sort allow expression of an ORF as a protein that contains the same amino and carboxy amino acids as in the native, uncloned, protein. When such a construct is fused in-frame with an amino-terminal protein tag, e.g., GST, the tag will have its own tis, thus tis-ATG-tag-tis-ATG-ORF-stop, and the bases comprising the tis of the ORF will be translated into amino acids between the tag and the ORF. In addition, some level of translation initiation may be expected in the interior of the mRNA (i.e., at the ORF's ATG and not the tag's ATG) resulting in a certain amount of native protein expression contaminating the desired protein.
DNA (lower case): tis1-atg-tag-tis2-atg-orf-stop
RNA (lower case, italics): tis1-atg-tag-tis2-atg-orf-stop
Protein (upper case): ATG-TAG-TIS2-ATG-ORF (tis1 and stop are not translated)+ contaminating ATG-ORF (translation of ORF beginning at tis2).
Using the methods disclosed herein, one skilled in the art can construct a vector containing a nucleic acid sequence encoding a polypeptide having a detectable activity (e.g., β-lactamase activity) adjacent to a recombination site permitting the in frame fusion of a nucleic acid sequence encoding a polypeptide having a detectable activity (e.g., β-lactamase activity) to the C- and/or N-terminus of the ORF of interest.
Given the ability to rapidly create a number of clones in a variety of vectors, there is a need in the art to maximize the number of ways a single cloned ORF can be expressed without the need to manipulate the construct itself. The present invention meets this need by providing materials and methods for the controlled expression of a C- and/or N-terminal fusion to a target ORF using one or more suppressor tRNAs to suppress the termination of translation at a stop codon. Thus, the present invention provides materials and methods in which a gene construct is prepared flanked with recombination sites.
The construct may be prepared with a sequence coding for a stop codon at the C-terminus of the ORF encoding the protein of interest. In some embodiments, a stop codon can be located adjacent to the ORF, for example, within the recombination site flanking the gene or at or near the 3′ end of the sequence of interest before a recombination site. The target gene construct can be transferred through recombination to various vectors that can provide various C-terminal or N-terminal tags (e.g., GFP, GST, His Tag, GUS, etc.) to the ORF of interest. In a particular embodiment of the invention, an ORF encoding a polypeptide of interest may be inserted into a vector comprising a nucleic acid sequence encoding a polypeptide having β-lactamase activity. When the stop codon is located at the carboxy terminus of the ORF, expression of the ORF with a “native” carboxy end amino acid sequence occurs under non-suppressing conditions (i.e., when the suppressor tRNA is not expressed) while expression of the ORF as a carboxy fusion protein occurs under suppressing conditions. Those skilled in the art will recognize that any suppressors and any codons could be used in the practice of the present invention. Suppressors may insert any amino acid at the position corresponding to the stop codon, for example, Ala, Arg, Asn, Asp, Cys, Gln, Glu, Gly, His, Ile, Leu, Lys, Met, Phe, Pro, Ser, Thr, Trp, Tyr, or Val may be inserted. In some embodiments, serine may be inserted.
In some embodiments, the gene coding for the suppressing tRNA may be incorporated into the vector from which the target ORF is to be expressed. In other embodiments, the gene for the suppressor tRNA may be in the genome of the host cell. In still other embodiments, the gene for the suppressor may be located on a separate nucleic acid molecule (e.g., plasmid, virus, linear nucleic acid molecule, etc.) and provided in trans. In embodiments of this type, the vector containing the suppressor gene may be a recombinant adenoviral vector and cells may be transduced with the viral vector.
In some embodiments, the nucleic acid molecule of the invention may be introduced into host cells as a vector (e.g., a plasmid, virus, etc) or may be stably integrated into the genome of the host cells. Suppressor tRNAs may be introduced into these cells using any of the methods described above.
More than one copy of a suppressor tRNA may be provided in all of the embodiments described herein. For example, a host cell may be provided that contains multiple copies of a gene encoding the suppressor tRNA. Alternatively, multiple gene copies of the suppressor tRNA under the same or different promoters may be provided in the same vector background as the target ORF of interest. In some embodiments, multiple copies of a suppressor tRNA may be provided in a different vector than the one containing the target ORF of interest. In other embodiments, one or more copies of the suppressor tRNA gene may be provided on the vector containing the ORF for the protein of interest and/or on another vector and/or in the genome of the host cell or in combinations of the above. When more than one copy of a suppressor tRNA gene is provided, the genes may be expressed from the same or different promoters that may be the same or different as the promoter used to express the ORF encoding the protein of interest.
In some embodiments, two or more different suppressor tRNA genes may be provided. In embodiments of this type one or more of the individual suppressors may be provided in multiple copies and the number of copies of a particular suppressor tRNA gene may be the same or different as the number of copies of another suppressor tRNA gene. Each suppressor tRNA gene, independently of any other suppressor tRNA gene, may be provided on the vector used to express the ORF of interest and/or on a different vector and/or in the genome of the host cell. A given tRNA gene may be provided in more than one place in some embodiments. For example, a copy of the suppressor tRNA may be provided on the vector containing the ORF of interest while one or more additional copies may be provided on an additional vector and/or in the genome of the host cell. When more than one copy of a suppressor tRNA gene is provided, the genes may be expressed from the same or different promoters that may be the same or different as the promoter used to express the ORF encoding the protein of interest and may be the same or different as a promoter used to express a different tRNA gene.
In some embodiments of the present invention, the target ORF of interest and the gene expressing the suppressor tRNA may be controlled by the same promoter. In other embodiments, the target ORF of interest may be expressed from a different promoter than the suppressor tRNA. Those skilled in the art will appreciate that, under certain circumstances, it may be desirable to control the expression of the suppressor tRNA and/or the target ORF of interest using a regulatable promoter. For example, either the target ORF of interest and/or the gene expressing the suppressor tRNA may be controlled by a promoter such as the lac promoter or derivatives thereof such as the tac promoter. In some embodiments, both the target ORF of interest and the suppressor tRNA gene are expressed from the T7 RNA polymerase promoter and, optionally, are expressed as part of one RNA molecule. In embodiments of this type, the portion of the RNA corresponding to the suppressor tRNA is processed from the originally transcribed RNA molecule by cellular factors.
In some embodiments, the expression of the suppressor tRNA gene may be under the control of a different promoter from that of the ORF of interest. In some embodiments, it may be possible to express the suppressor gene before the expression of the target ORF. This would allow levels of suppressor to build up to a high level, before they are needed to allow expression of a fusion protein by suppression of a the stop codon. For example, in embodiments of the invention where the suppressor gene is controlled by a promoter inducible with IPTG, the target ORF is controlled by the T7 RNA polymerase promoter and the expression of the T7 RNA polymerase is controlled by a promoter inducible with an inducing signal other than IPTG, e.g., NaCl, one could turn on expression of the suppressor tRNA gene with IPTG prior to the induction of the T7 RNA polymerase gene and subsequent expression of the ORF of interest. In some embodiments, the expression of the suppressor tRNA might be induced about 15 minutes to about one hour before the induction of the T7 RNA polymerase gene. In one embodiment, the expression of the suppressor tRNA may be induced from about 15 minutes to about 30 minutes before induction of the T7 RNA polymerase gene. In some embodiments, the expression of the T7 RNA polymerase gene is under the control of an inducible promoter.
In additional embodiments, the expression of the target ORF of interest and the suppressor tRNA can be arranged in the form of a feedback loop. For example, the target ORF of interest may be placed under the control of the T7 RNA polymerase promoter while the suppressor gene is under the control of both the T7 promoter and the lac promoter. The T7 RNA polymerase gene itself is also under the control of both the T7 promoter and the lac promoter. In addition, the T7 RNA polymerase gene has an amber stop mutation replacing a normal tyrosine codon, e.g., the 28th codon (out of 883). No active T7 RNA polymerase can be made before levels of suppressor are high enough to give significant suppression. Then expression of the polymerase rapidly rises, because the T7 polymerase expresses the suppressor gene as well as itself. In other embodiments, only the suppressor gene is expressed from the T7 RNA polymerase promoter. Embodiments of this type would give a high level of suppressor without producing an excess amount of T7 RNA polymerase. In other embodiments, the T7 RNA polymerase gene has more than one amber stop mutation. This will require higher levels of suppressor before active T7 RNA polymerase is produced.
In some embodiments of the present invention it may be desirable to have more than one stop codon suppressible by more than one suppressor tRNA. A recombinant nucleic acid molecule may be constructed so as to permit the regulatable expression of N- and/or C-terminal fusions of a protein of interest from the same construct. A nucleic acid molecule may comprise a first tag sequence expressed from a promoter and may include a first stop codon in the same reading frame as the tag. The stop codon may be located anywhere in the tag sequence and in particular may be located at or near the C-terminal of the tag sequence. The stop codon may also be located in a recombination site or in an internal ribosome entry sequence (IRES). The nucleic acid molecule may also include a sequence of interest which may comprising a ORF of interest that includes a second stop codon. The first tag and the ORF of interest may be in the same reading frame although inclusion of a sequence that causes frame shifting to bring the first tag into the same reading frame as the ORF of interest is within the scope of the present invention. The second stop codon may be in the same reading frame as the ORF of interest and may be located at or near the end of the coding sequence for the ORF. The second stop codon may optionally be located within a recombination site located 3′ to the sequence of interest. The construct may also include a second tag sequence in the same reading frame as the ORF of interest and the second tag sequence may optionally include a third stop codon in the same reading frame as the second tag. A transcription terminator and/or a polyadenylation sequence may be included in the construct after the coding sequence of the second tag. The first, second and third stop codons may be the same or different. In some embodiments, all three stop codons are different. In embodiments where the first and the second stop codons are different, the same construct may be used to express an N-terminal fusion, a C-terminal fusion and the native protein by varying the expression of the appropriate suppressor tRNA. For example, to express the native protein, no suppressor tRNAs are expressed and protein translation is controlled by an appropriately located IRES. When an N-terminal fusion is desired, a suppressor tRNA that suppresses the first stop codon is expressed while a suppressor tRNA that suppresses the second stop codon is expressed in order to produce a C-terminal fusion. In some instances it may be desirable to express a doubly tagged protein of interest in which case suppressor tRNAs that suppress both the first and the second stop codons may be expressed.
The invention also relates to host cells comprising one or more of the nucleic acid molecules invention containing one or more nucleic acid sequences encoding a polypeptide having a detectable activity and/or one or more other sequences of interest (e.g., two, three, four, five, seven, ten, twelve, fifteen, twenty, thirty, fifty, etc.). Representative host cells that may be used according to this aspect of the invention include, but are not limited to, bacterial cells, yeast cells, plant cells and animal cells. In particular embodiments, bacterial host cells include Escherichia spp. cells (particularly E. coli cells and most particularly E. coli strains DH10B, Stb12, DH5α, DB3, DB3.1 (e.g., E. coli LIBRARY EFFICIENCY® DB3.1™ Competent Cells; Invitrogen Corporation, Carlsbad, Calif.), DB4, DB5, JDP682 and ccdA-over (see U.S. application Ser. No. 09/518,188, filed Mar. 2, 2000, and U.S. provisional Application No. 60/475,004, filed Jun. 3, 2003, by Louis Leong et al., entitled “Cells Resistant to Toxic Genes and Uses Thereof,” the disclosures of which are incorporated by reference herein in their entireties); Bacillus spp. cells (particularly B. subtilis and B. megaterium cells), Streptomyces spp. cells, Erwinia spp. cells, Klebsiella spp. cells, Serratia spp. cells (particularly S. marcessans cells), Pseudomonas spp. cells (particularly P. aeruginosa cells), and Salmonella spp. cells (particularly S. typhimurium and S. typhi cells). Suitable animal host cells include insect cells (most particularly Drosophila melanogaster cells, Spodoptera frugiperda Sf9 and Sf21 cells and Trichoplusa High-Five cells), nematode cells (particularly C. elegans cells), avian cells, amphibian cells (particularly Xenopus laevis cells), reptilian cells, and mammalian cells (most particularly NIH3T3, 293, CHO, COS, VERO, BHK and human cells). Suitable yeast host cells include Saccharomyces cerevisiae cells and Pichia pastoris cells. These and other suitable host cells are available commercially, for example, from Invitrogen Corporation, (Carlsbad, Calif.), American Type Culture Collection (Manassas, Va.), and Agricultural Research Culture Collection (NRRL; Peoria, Ill.).
Nucleic acid molecules to be used in the present invention may comprise one or more origins of replication (ORIs), and/or one or more selectable markers. In some embodiments, molecules may comprise two or more ORIs at least two of which are capable of functioning in different organisms (e.g., one in prokaryotes and one in eukaryotes). For example, a nucleic acid may have an ORI that functions in one or more prokaryotes (e.g., E. coli, Bacillus, etc.) and another that functions in one or more eukaryotes (e.g., yeast, insect, mammalian cells, etc.). Selectable markers may likewise be included in nucleic acid molecules of the invention to allow selection in different organisms. For example, a nucleic acid molecule may comprise multiple selectable markers, one or more of which functions in prokaryotes and one or more of which functions in eukaryotes.
Methods for introducing the nucleic acids molecules of the invention into the host cells described herein, to produce host cells comprising one or more of the nucleic acids molecules of the invention, will be familiar to those of ordinary skill in the art. For instance, the nucleic acid molecules of the invention may be introduced into host cells using well known techniques of infection, transduction, electroporation, transfection, and transformation. The nucleic acid molecules of the invention may be introduced alone or in conjunction with other nucleic acid molecules and/or vectors and/or proteins, peptides or RNAs. Alternatively, the nucleic acid molecules of the invention may be introduced into host cells as a precipitate, such as a calcium phosphate precipitate, or in a complex with a lipid. Electroporation also may be used to introduce the nucleic acid molecules of the invention into a host. Likewise, such molecules may be introduced into chemically competent cells such as E. coli. If the vector is a virus, it may be packaged in vitro or introduced into a packaging cell and the packaged virus may be transduced into cells. Thus nucleic acid molecules of the invention may contain and/or encode one or more packaging signal (e.g., viral packaging signals that direct the packaging of viral nucleic acid molecules). Hence, a wide variety of techniques suitable for introducing the nucleic acid molecules and/or vectors of the invention into cells in accordance with this aspect of the invention are well known and routine to those of skill in the art. Such techniques are reviewed at length, for example, in Sambrook, J., et al., Molecular Cloning, a Laboratory Manual, 2nd Ed., Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory Press, pp. 16.30-16.55 (1989), Watson, J. D., et al., Recombinant DNA, 2nd Ed., New York: W.H. Freeman and Co., pp. 213-234 (1992), and Winnacker, E.-L., From Genes to Clones, New York: VCH Publishers (1987), which are illustrative of the many laboratory manuals that detail these techniques and which are incorporated by reference herein in their entireties for their relevant disclosures.
In another aspect, the invention provides kits that may be used in conjunction with methods the invention. Kits according to this aspect of the invention may comprise one or more containers, which may contain one or more components selected from the group consisting of one or more nucleic acid molecules (e.g., one or more nucleic acid molecules comprising one or more nucleic acid sequence encoding a polypeptide having a detectable activity) of the invention, one or more primers, the molecules and/or compounds of the invention, one or more polymerases, one or more reverse transcriptases, one or more recombination proteins (or other enzymes for carrying out the methods of the invention), one or more topoisomerases, one or more buffers, one or more detergents, one or more restriction endonucleases, one or more nucleotides, one or more terminating agents (e.g., ddNTPs), one or more transfection reagents, pyrophosphatase, and the like. Kits of the invention may also comprise written instructions for carrying out one or more methods of the invention.
The present invention also provides kits that contain components useful for conveniently practicing the methods of the invention. In one embodiment, a kit of the invention contains a first nucleic acid molecule, which comprises a nucleic acid sequence encoding a polypeptide having a detectable activity, and contains one or more topoisomerase recognition sites and/or one or more covalently attached topoisomerase enzymes. Nucleic acid molecules according to this aspect of the invention may further comprise one or more recombination sites. In some embodiments, the nucleic acid molecule comprises a topoisomerase-activated nucleotide sequence. The topoisomerase-charged nucleic acid molecule may comprise a 5′ overhanging sequence at either or both ends and, the overhanging sequences may be the same or different. Optionally, each of the 5′ termini comprises a 5′ hydroxyl group.
In one embodiment, a kit of the invention contains a first nucleic acid molecule, which comprises a nucleic acid sequence encoding a polypeptide having a detectable activity, and contains one or more recombination sites. Nucleic acid molecules according to his aspect of the invention may further comprise one or more topoisomerase sites and/or topoisomerase enzymes.
In addition, the kit can contain at least a nucleotide sequence (or complement thereof) comprising a regulatory element, which can be an upstream or downstream regulatory element, or other element, and which contains a topoisomerase recognition site at one or both ends. In particular embodiments, kits of the invention contain a plurality of nucleic acid molecules, each comprising a different regulatory element or other element, for example, a sequence encoding a tag or other detectable molecule or a cell compartmentalization domain. The different elements can be different types of a particular regulatory element, for example, constitutive promoters, inducible promoters and tissue specific promoters, or can be different types of elements including, for example, transcriptional and translational regulatory elements, epitope tags, and the like. Such nucleic acid molecules can be topoisomerase-activated, and can contain 5′ overhangs or 3′ overhangs that facilitate operatively covalently linking the elements in a predetermined orientation, particularly such that a polypeptide such as a selectable marker is expressible in vitro or in one or more cell types.
The kit also can contain primers, including first and second primers, such that a primer pair comprising a first and second primer can be selected and used to amplify a desired ds recombinant nucleic acid molecule covalently linked in one or both strands, generated using components of the kit. For example, the primers can include first primers that are complementary to elements that generally are positioned at the 5′ end of a generated ds recombinant nucleic acid molecule, for example, a portion of a nucleic acid molecule comprising a promoter element, and second primers that are complementary to elements that generally are positioned at the 3′ end of a generated ds recombinant nucleic acid molecule, for example, a portion of a nucleic acid molecule comprising a transcription termination site or encoding an epitope tag. Depending on the elements selected from the kit for generating a ds recombinant nucleic acid molecule covalently linked in both strands, the appropriate first and second primers can be selected and used to amplify a full length functional construct.
In another embodiment, a kit of the invention contains a plurality of different elements, each of which can comprise one or more recombination sites and/or can be topoisomerase-activated at one or both ends, and each of which can contain a 5′-overhanging sequence or a 3′-overhanging sequence or a combination thereof. The 5′ or 3′ overhanging sequences can be unique to a particular element, or can be common to plurality of related elements, for example, to a plurality of different promoter element. In particular embodiments, the 5′ overhanging sequences of elements are designed such that one or more elements can be operatively covalently linked to provide a useful function, for example, an element comprising a Kozak sequence and an element comprising a translation start site can have complementary 5′ overhangs such that the elements can be operatively covalently linked according to a method of the invention.
The plurality of elements in the kit can comprise any elements, including transcription or translation regulatory elements; elements required for replication of a nucleotide sequence in a bacterial, insect, yeast, or mammalian host cell; elements comprising recognition sequences for site specific nucleic acid binding proteins such as restriction endonucleases or recombinases; elements encoding expressible products such as epitope tags or drug resistance genes; and the like. As such, a kit of the invention provides a convenient source of different elements that can be selected depending, for example, on the particular cells that a construct generated according to a method of the invention is to be introduced into or expressed in. The kit also can contain PCR primers, including first and second primers, which can be combined as described above to amplify a ds recombinant nucleic acid molecule covalently linked in one or both strands, generated using the elements of the kit. Optionally, the kit further contains a site specific topoisomerase in an amount useful for covalently linking in at least one strand, a first nucleic acid molecule comprising a topoisomerase recognition site to a second (or other) nucleic acid molecule, which can optionally be topoisomerase-activated nucleic acid molecules or nucleotide sequences that comprise a topoisomerase recognition site.
In still another embodiment, a kit of the invention contains a first nucleic acid molecule, which comprises a nucleic acid sequence encoding a polypeptide having a detectable activity, and contains a topoisomerase recognition site and/or a recombination site at each end; a first and second PCR primer pair, which can produce a first and second amplification products that can be covalently linked in one or both strands, to the first nucleic acid molecule in a predetermined orientation according to a method of the invention.
Kits of the invention may further comprise (1) instructions for performing one or more methods described herein and/or (2) a description of one or more compositions described herein. These instructions and/or descriptions may be in printed form. For example, these instructions and/or descriptions may be in the form of an insert which is present in kits of the invention.
It will be understood by one of ordinary skill in the relevant arts that other suitable modifications and adaptations to the methods and applications described herein are readily apparent from the description of the invention contained herein in view of information known to the ordinarily skilled artisan, and may be made without departing from the scope of the invention or any embodiment thereof. Having now described the present invention in detail, the same will be more clearly understood by reference to the following examples, which are included herewith for purposes of illustration only and are not intended to be limiting of the invention.
The present invention provides a highly efficient cloning strategy for the direct insertion of amplified promoter sequences (for example, using Taq polymerase) into a reporter vector. One non-limiting example of materials suitable for the practice of the invention may be obtained from Invitrogen Corporation, Carlsbad, Calif. under the trade name pGeneBLAzer™ TOPO® TA Expression Kits. In one aspect, promoter sequences can be inserted into a nucleic acid molecule upstream of the β-lactamase reporter gene. Resultant nucleic acid molecules may then be transfected into suitable host cells (e.g., mammalian cells) and assayed for promoter function and strength in vivo or in vitro. β-lactamase activity may be determined using any technique known to those skilled in the art, for example, using the GeneBLAzer™ In Vivo or In Vitro Detection Kit, available from Invitrogen Corporation, Carlsbad, Calif. In contrast to previously employed methods, no ligase, post-PCR procedures, or PCR primers containing specific sequences are required.
In some embodiments, suitable nucleic acid molecules for practicing the methods of the invention may be vectors (e.g., plasmid vectors such as pGeneBLAzer-TOPO™).
Materials and methods of the invention (e.g., GeneBLAzer™ Technology and the GeneBLAzer™ Detection System) may be used as described herein as a reporter of gene expression in mammalian cells. Materials and methods of the invention are suitable for use as a sensitive reporter of gene expression in living host cells (e.g., mammalian cells) using fluorescence microscopy. Materials and methods of the invention may provide a ratiometric readout that minimizes differences due to variability in cell number, substrate concentration, fluorescence intensity, and emission sensitivity. Materials and methods of the invention are compatible with a wide variety of in vivo and in vitro applications including microplate-based transcriptional assays and flow cytometry. Materials and methods of the invention provides flexible and simple assay development platforms for gene expression in host cells (e.g., mammalian cells). In particular, materials and methods of the invention may use a non-toxic substrate that allows continued cell culturing after quantitative analysis.
In a particular embodiment, methods of the invention may use one or more topoisomerase enzymes to join a nucleic acid sequence to be assayed for promoter activity to a nucleic acid sequence encoding a polypeptide having a detectable activity. A suitable example of a topoisomerase is topoisomerase I from Vaccinia virus, which binds to duplex DNA at specific sites and cleaves the phosphodiester backbone after 5′-CCCTT in one strand (see, Shuman, S. (1994) J. Biol. Chem. 269, 32678-32684). The energy from the broken phosphodiester backbone is conserved by formation of a covalent bond between the 3′ phosphate of the cleaved strand and a tyrosyl residue (Tyr-274) of topoisomerase I. The phospho-tyrosyl bond between the DNA and enzyme can subsequently be attacked by the 5′ hydroxyl of the original cleaved strand, reversing the reaction and releasing topoisomerase. TOPO® Cloning exploits this reaction to efficiently clone PCR products.
In a particular embodiment, the pGeneBLAzer-TOPO® vector is linearized and has single 3′ thymidine (T) overhangs for TA Cloning®. In embodiments of this type, topoisomerase I may be covalently bound to the vector (this is referred to as “activated vector”). As is known in the art, Taq polymerase has a nontemplate-dependent terminal transferase activity that adds a single deoxyadenosine (A) to the 3′ ends of PCR products. In a particular embodiment, a linearized vector may be supplied (e.g., as a component in a kit) and may have overhanging 3′ deoxythymidine (T) residues. Embodiments of this type may allow PCR products to ligate efficiently into the vector. Ligation of the vector with a PCR product containing 3′ A-overhangs is very efficient and occurs spontaneously within 5 minutes at room temperature. After the topoisomerase-mediated joining of the nucleic acid molecules, the resultant nucleic acid molecule may be introduced into a suitable host cell (e.g., transformed into chemically competent cells or electroporated directly into electrocompetent cells).
The materials and methods of the invention facilitate fluorescent detection of β-lactamase reporter activity in host cells (e.g., mammalian cells). In some embodiments, materials of the invention may comprise a β-lactamase reporter gene, bla(M), a truncated form of the E. coli bla gene. When fused to promoter sequences (e.g., in the pGeneBLAzer-TOPO® vector), the bla(M) gene functions as a reporter of promoter activity in host cells (e.g., mammalian cells).
Materials and methods of the of the invention may also comprise one or more fluorescence resonance energy transfer (FRET)-enabled substrates (e.g., CCF2) to facilitate fluorescence detection of β-lactamase reporter activity. In the absence or presence of β-lactamase reporter activity, cells loaded with the CCF2 substrate fluoresce green or blue, respectively. Comparing the ratio of blue to green fluorescence in a population of live cells or in a cell extract prepared from a sample to a negative control provides a means to quantitate gene expression.
In some embodiments, a β-lactamase for use in the present invention may be the product encoded by the ampicillin resistance gene (bla), which is the bacterial enzyme that hydrolyzes penicillins and cephalosporins. The bla gene is present in many cloning vectors and allows ampicillin selection in E. coli. β-lactamase is not found in mammalian cells.
In some embodiments, materials and methods of the invention may use a modified bla gene as a reporter in mammalian cells. One example is a bla gene derived from the E. coli TEM-1 gene present in many cloning vectors (see, Zlokarnik, et al. (1998) Science 279, 84-88), which has been modified in that 72 nucleotides encoding the first 24 amino acids of β-lactamase were deleted from the N-terminal region of the gene. These 24 amino acids comprise the bacterial periplasmic signal sequence, and deleting this region allows cytoplasmic expression of β-lactamase in mammalian cells. The amino acid at position 24 was mutated from His to Asp to create an optimal Kozak sequence for improved translation initiation. As used herein, this modified reporter gene is named bla(M) and the amino acid sequence is provided in
Methods of the invention may comprise designing PCR primers to amplify a desired nucleic acid sequence to be assayed as for promoter activity; amplifying the desired nucleic acid sequence; cloning the nucleic acid sequence into a vector of the invention (e.g., pGeneBLAzer-TOPO®). Methods may further entail transforming the topoisomerase-mediated cloning reaction into competent cells (e.g., One Shot® TOP10 E. coli, Invitrogen Corporation, Carlsbad, Calif.) and selecting for transformants on LB agar plates containing 100 μg/ml ampicillin. Transformants can be screened for the presence and orientation of the nucleic acid sequence to be assayed for promoter activity using standard techniques, for example, by restriction digestion, PCR, or sequencing. A plasmid having the correct nucleic acid sequence in the correct orientation may be purified for transfection. The purified plasmid may be introduced into a suitable host cell. A stable cell line containing the plasmid may be isolated. Transformed host cells may be assayed for β-lactamase activity, for example, using the appropriate GeneBLAzer™ Detection Kit.
In particular embodiments, materials and methods of the invention may be used to analyze one or more of tissue and cell-specific promoter function, transcriptional enhancers in a known promoter, and/or deletions within a promoter. One skilled in the art will appreciate that when analyzing promoters in a reporter vector, it is important to realize that sequences within the native gene can influence regulation of its own promoter. In addition, sequences within the reporter gene can also affect transcription from the promoter under study. It is recommended that any observations of transcriptional control of the fusion gene be verified by comparison with expression of the native gene expressed from the same promoter. Techniques well known in the art (e.g., Si mapping) can be used to confirm that the subcloned promoter initiates transcription at the correct site. For more information about Si mapping, see Ausubel, et al. (1994) Current Protocols in Molecular Biology, pages 4.6.1 to 4.6.13, New York: Greene Publishing Associates and Wiley-Interscience. Since initiation of translation in eukaryotes occurs at the first available AUG codon, it is important that there are no AUG codons between the start of transcription and the AUG of the reporter gene.
The selection of suitable primers for use in the amplification of a sequence of interest to be assayed for promoter activity is routine in the art. Unique restriction sites may be included in the 5′ and 3′ primers to excise the fragment or facilitate analysis once it is TOPO® Cloned. Primers for the amplification of a sequence of interest should not be 5′-phosphorylated. Phosphates will inhibit topoisomerase I and the synthesized PCR product will not ligate into the pGeneBLAzer-TOPO® vector.
Any suitable DNA polymerase or combination of DNA polymerases may be used to amplify the sequence of interest. For example, mixtures of Taq polymerase and a proofreading polymerase (e.g., Pfu DNA polymerase) may be used. When mixtures are used, Taq may be used in excess of a 10:1 ratio to ensure the presence of 3′ A-overhangs on the PCR product. One suitable DNA polymerase for use in methods of the invention is Platinum® Taq DNA Polymerase High Fidelity available from Invitrogen Corporation, Carlsbad, Calif. If mixtures are used that do not have enough Taq polymerase or a proofreading polymerase is used without Taq polymerase, 3′ A-overhangs can be added after amplification. One suitable method for adding 3′-A overhangs is to add Taq DNA polymerase to the amplification reaction mixture. For example, 0.7-1 unit of Taq polymerase may be added to each tube and then the tubes may be incubated under suitable conditions to allow addition of 3′-A by Taq polymerase. One non-limiting example of suitable conditions is to add Taq polymerase to the tube containing the amplification reaction and to incubate at 72° C. for 8-10 minutes without cycling the temperature. Typically, it is not necessary to purify the amplification product or change buffers prior to the addition of Taq polymerase.
One skilled in the art can select suitable amplification conditions for a sequence of interest using routine experimentation. One example of a suitable set of amplification conditions follows. A 50 μl PCR reaction may be set up, for example, containing 10-100 ng DNA Template, 5 μl of 10×PCR Buffer, 0.5 μl of 50 mM dNTPs, 100-200 ng of each primer, sterile water can be added to a final volume of 49 μl, and 1 μl of Taq Polymerase at a concentration of 1 unit/μl can be added.
As will be appreciated by those skilled in the art, these conditions may be varied. For example, less DNA may be used if plasmid DNA is used as a template and more DNA may be used if genomic DNA is used as a template. Selection of suitable cycling parameters (e.g., time and temperature of annealing and extension reactions) are routine in the art and may be adjusted for any specific primers and template.
A 7 to 30 minute extension at 72° C. after the last cycle may be used to ensure that all PCR products are full length and 3′ adenylated. The amplification product may be checked, for example, by agarose gel electrophoresis. Conditions may adjusted to produce a single, discrete band on an agarose gel. If samples are to be stored (e.g., overnight) before proceeding with TOPO® Cloning, samples may be extracted with phenol-chloroform to remove the polymerases. After phenol-chloroform extraction, the DNA may be precipitated with ethanol and resuspended in TE buffer to the starting volume of the amplification reaction.
Optionally, if the amplification reaction does not produce a single discrete band, the amplification product may be purified, for example, from an agarose gel prior to insertion into nucleic acid molecule of the invention. When an amplification product is to be purified, nuclease contamination and long exposure to UV light should be avoided. Alternatively, the amplification conditions may be varied to eliminate multiple bands and smearing as is known in the art (see, for example, Innis, et al. (1990) PCR Protocols: A Guide to Methods and Applications, Academic Press, San Diego, Calif.) Commercially available materials may be used to optimize the amplification reaction, for example, The PCR Optimizer™ Kit (Catalog no. K1220-01) is available from Invitrogen Corporation, Carlsbad, Calif.
In some embodiments, salt may be included in a topoisomerase reaction to join a nucleic acid molecule having a sequence of interest and a nucleic acid molecule having a nucleic acid sequence encoding a polypeptide having a detectable activity. For example, including salt (200 mM NaCl, 10 mM MgCl2) in the TOPO® Cloning reaction increases the number of transformants 2- to 3-fold. In the presence of salt, incubation times of greater than 5 minutes can also increase the number of transformants. This is in contrast to experiments without salt where the number of transformants decreases as the incubation time increases beyond 5 minutes. Without wishing to be bound by theory, including salt allows for longer incubation times because it prevents topoisomerase I from rebinding and potentially nicking the DNA after ligating the PCR product and dissociating from the DNA. The result is more intact molecules, leading to higher transformation efficiencies.
One skilled in the art will appreciate that the amount of salt that may be added to a topoisomerase reaction may vary depending on the method used to introduced the topoisomerase joined nucleic acid molecules into a host cell. For TOPO® Cloning and transformation into chemically competent E. coli, adding sodium chloride and magnesium chloride to a final concentration of 200 mM NaCl, 10 mM MgCl2 in the TOPO® Cloning reaction may increase the number of colonies over time. A salt solution (e.g., 1.2 M NaCl; 0.06 M MgCl2) can be used to adjust the TOPO® Cloning reaction to the recommended concentration of NaCl and MgCl2. For transformation of electrocompetent E. coli, the amount of salt in the TOPO® Cloning reaction must be reduced to 50 mM NaCl, 2.5 mM MgCl2 to prevent arcing. For example, the salt solution can be diluted 4-fold with sterile water to prepare a 300 mM NaCl, 15 mM MgCl2 solution for convenient addition to the TOPO® Cloning reaction.
Suitable conditions for topoisomerase-mediated joining of nucleic acid molecules are known to those skilled in the art. Non-limiting examples of suitable conditions follow. When the joined nucleic acid molecules are to be introduced into a competent host cell by transformation, a suitable set of conditions is a 6 μl reaction volume containing 0.5 to 4 μl of amplification product, 1 μl of the a 1.2 M NaCl; 0.06 M MgCl2 salt solution, sterile water to a final volume of 5 μl, and 1 μl of topoisomerase charged vector. For electroporation, 1 μl of a 1:4 dilution of the 1.2 M NaCl; 0.06 M MgCl2 may be used. The reagents may be added and gently mixed and incubated for 5 minutes at room temperature. For most applications, 5 minutes will yield sufficient colonies for analysis. The length of the TOPO® Cloning reaction can be varied from 30 seconds to 30 minutes. For routine subcloning of PCR products, 30 seconds may be sufficient. For large PCR products (>1 kb) or if TOPO® Cloning a pool of PCR products, increasing the reaction time will yield more colonies. After incubation at room temperature, the reaction mixture may be placed on ice and the joined nucleic acid molecules may be introduced into a suitable host cell using standard techniques. Optionally, the TOPO® Cloning reaction can be stored at −20° C. overnight.
Other factors that are known to those skilled in the art may impact the efficiency with which a nucleic acid molecule having a nucleic acid sequence to be assayed for promoter activity is joined with a nucleic acid molecule having a nucleic acid sequence encoding a polypeptide having a detectable activity. For example, the pH of the amplification reaction may affect the amount of amplification product produced. If the pH of the PCR reaction is too high, the pH of the PCR amplification reaction may be adjusted with 1 M Tris-HCl, pH 8. Another factor is incomplete extension during PCR. This may be adjusted by including a final extension step of 7 to 30 minutes during PCR. Longer PCR products will need a longer extension time. Note that Taq polymerase is less efficient at adding a nontemplate 3′ A next to another A. Taq is most efficient at adding a nontemplate 3′ A next to a C. Primers may be designed so that they contain a 5′ G instead of a 5′ T (see, Brownstein, et al. (1996) BioTechniques 20, 1004-1010). When cloning large inserts (>3 kb), it may be desirable to gel-purify the insert. The amount of PCR product may be adjusted by concentrating or diluting the PCR product as needed. Up to 4 μl of the PCR reaction may be added to the TOPO® Cloning reaction. If false positives are observed, it may be desirable to gel purify the PCR product. The size of promoter sequences cloned can impact the efficiency. For large plasmids, electroporation to transform into E. coli may provide an increased number of colonies. Electrocompetent TOP10 cells are commercially available from Invitrogen Corporation, Carlsbad, Calif.
One skilled in the art will appreciate that the above-described protocol can be varied. For example, the amount of time spent on various steps can be varied. For example, the TOPO® Cloning reaction may be incubated for only 30 seconds instead of 5 minutes. When TOPO® Cloning large PCR products, toxic genes, or cloning a pool of PCR products, it may be desirable to produce more transformants to obtain the desired clones. To increase the number of colonies the salt-supplemented TOPO® Cloning reaction may be incubated for longer time (e.g., for 20 to 30 minutes instead of 5 minutes). Increasing the incubation time of the salt-supplemented TOPO® Cloning reaction allows more molecules to ligate, increasing the transformation efficiency. Addition of salt appears to prevent topoisomerase from rebinding and nicking the DNA after it has ligated the PCR product and dissociated from the DNA. To clone dilute PCR products, it may be desirable to increase the amount of the PCR product used, incubate the TOPO® Cloning reaction for 20 to 30 minutes, and/or concentrate the PCR product by precipitation.
Any protocol used to introduce nucleic acid molecules into host cells known to those skilled in the art may be used. Chemically competent cells may be made using standard techniques or commercially available cells may be used. An example of a suitable protocol for introducing nucleic acid molecules into commercially available competent cells is as follows. 2 μl of the TOPO® Cloning reaction from above may be added to a vial of One Shot® TOP10 Chemically Competent E. coli (Invitrogen Corporation, Carlsbad, Calif.) and mixed gently. The cells should not be mixed by pipetting up and down. The nucleic acid molecule: cell mixture may be incubated on ice for 5 to 30 minutes. Longer incubations on ice seem to have a minimal effect on transformation efficiency. The length of the incubation may be varied. The mixture may be heat shocked for 30 seconds at 42° C. without shaking. After heat shock, the mixture should be immediately transferred to ice. 250 μl of room temperature S.O.C. medium may be added. The tube may be tightly capped and shaken horizontally (200 rpm) at 37° C. for 1 hour. 25-200 μl from each transformation may be spread on a pre-warmed selective plate and incubated overnight at 37° C. Two different volumes (e.g., 20 μl and 200 μl) can be plated to ensure that at least one plate will have well-spaced colonies. An efficient TOPO® Cloning reaction will produce hundreds of colonies. Pick ˜10 colonies for analysis.
Any protocol used to introduce nucleic acid molecules into host cells known to those skilled in the art may be used. Electrocompetent cells may be made using standard techniques or commercially available cells may be used. An example of a suitable protocol for introducing nucleic acid molecules into electrocompetent cells is as follows. 2 μl of the TOPO® Cloning reaction described above may be added to 50 μl of electrocompetent E. coli and mixed gently. The cells should not be mixed by pipetting up and down. The formation of bubbles should be avoided. The mixture of DNA and electrocompetent cells can be transferred into a 0.1 cm cuvette. Electroporate samples using standard protocols and settings. 250 μl of room temperature S.O.C. medium may be added immediately. The solution can be transferred to a 15 ml snap-cap tube (i.e. Falcon) and shaken for at least 1 hour at 37° C. to allow expression of the antibiotic resistance marker. 10-50 μl from each transformation can be spread on a pre-warmed selective plates and incubated overnight at 37° C. To ensure even spreading of small volumes, add 20 μl of S.O.C. Medium. Two different volumes may be plated to ensure that at least one plate will have well-spaced colonies. An efficient TOPO® Cloning reaction will produce hundreds of colonies. Pick ˜10 colonies for analysis.
Individual colonies may be picked and overnight cultures grown (e.g., 3-5 mL cultures in LB medium containing 100 μg/mL ampicillin). Plasmids may be isolated using standard techniques. Analyze transformants for the presence of the sequence of interest to be assayed for promoter activity using any technique known in the art (e.g., restriction digests, sequencing, PCR, etc.). For example, the sequence of the pGeneBLAzer™ TOPO® vector is provided above. Primers can be designed from the sequence provided to sequence or PCR amplify a sequence of interest inserted into the vector to verify the presence of the sequence of interest in the selected clones.
Once a desired nucleic acid molecule has been produced in which a sequence of interest to be assayed for promoter activity is operably joined to a sequence encoding a polypeptide having a detectable activity, the desired nucleic acid molecule, which may be a plasmid, may be introduced into a suitable host cell (e.g., a mammalian cell). Plasmid DNA for transfection into eukaryotic cells must be very clean and free from phenol and sodium chloride. Contaminants will kill the cells and salt will interfere with lipid complexing decreasing transfection efficiency. Plasmid DNA (up to 200 μg) may be isolated using the S.N.A.P.™ MidiPrep Kit (Invitrogen Corporation, Carlsbad, Calif., Catalog no. K1910-01) or CsCl gradient centrifugation.
For analysis of promoter activity of a sequence of interest, positive and negative controls may be included to evaluate expression and detection β-lactamase. A negative control can be either a mock transfection or a pGeneBLAzer-TOPO® construct containing non-promoter DNA sequences (i.e. stuffer DNA).
For a positive control, the pGeneBLAzer™/UbC plasmid described above may be used. In this vector, the human ubiquitin C (UbC) promoter (see, Nenoi, et al. (1996) Gene 175, 179-185) controls expression of the β-lactamase reporter gene. This plasmid may be propagated by transformation into a recA, endA E. coli strain such as TOP10, DH5α, or equivalent. Transformants can be selected on LB agar plates containing 100 μg/ml ampicillin. A glycerol stock of a transformant containing plasmid may be prepared for long-term storage.
Nucleic acid molecules may be introduced into host cells using any technique known to those skilled in the art. Transfection protocols may be determined empirically or may be obtained from original references or the supplier of the cell line. Factors that may influence the transfection efficiency of a host cell include, but are not limited to, medium requirements, timing of passaging of cells, and the dilution of the cells when passaged. Further information is provided in Ausubel, (1994) Current Protocols in Molecular Biology. Suitable transfection methods for include calcium phosphate (see, Chen, C., and Okayama, H. (1987) Mol. Cell. Biol. 7, 2745-2752, Wigler, et al. (1977) Cell 11, 223-232), lipid-mediated (see, Feigner, et al. (1989) Proc. West. Pharmacol. Soc. 32, 115-121; and Feigner, P. L. and Ringold, G. M. (1989) Nature 337, 387-388), and electroporation (see, Chu, et al. (1987) Nucleic Acids Res. 15, 1311-1326; and Shigekawa, K., and Dower, W. J. (1988) BioTechniques 6, 742-751). One suitable transfection reagent is Lipofectamine™ 2000 (Invitrogen Corporation, Carlsbad, Calif. Catalog no. 11668-027).
In some embodiments, nucleic acid molecules produced using methods of the invention may be used to generate stable cell lines comprising the nucleic acid molecules. For example, nucleic acid molecules of the invention may comprise a selectable marker that may be used to select for cells containing the nucleic acid molecule of the invention. One example is the pGeneBLAzer-TOPO® vector that contains the neomycin resistance gene to allow selection of stable cell lines using Geneticin®. To create stable cell lines, transfect the nucleic acid molecule of the invention into the host cell line (e.g., mammalian cell line) of choice and select for foci using Geneticin®. Geneticin® blocks protein synthesis in mammalian cells by interfering with ribosomal function. It is an aminoglycoside, similar in structure to neomycin, gentamycin, and kanamycin. Expression in mammalian cells of the bacterial aminoglycoside phosphotransferase gene (APH), derived from Tn5, results in detoxification of Geneticin® (see, Southern, P. J., and Berg, P. (1982) J. Molec. Appl. Gen. 1, 327-339).
Geneticin® is commercially available (e.g., from Invitrogen Corporation, Carlsbad, Calif.). A stock of Geneticin® may be prepared (e.g., 50 mg/ml in buffer such as 100 mM HEPES, pH 7.3). Sufficient stock solution may be added to bring the concentration in the medium to about 100 to about 1000 μg/ml of Geneticin® in complete growth medium. Varying concentrations of Geneticin® may be tested on particular cell lines to determine the concentration that kills the particular cell line (i.e., a kill curve). Cells differ in their susceptibility to Geneticin®. Cells will divide once or twice in the presence of lethal doses of Geneticin®, so the effects of the drug take several days to become apparent. Complete selection can take from 2 to 4 weeks of growth in selective medium.
Once an appropriate Geneticin® concentration has been determined for a particular cell line, a stable cell line comprising an nucleic acid molecule of the invention may be prepared. For example, a cell line of interest may be transfected with a nucleic acid molecule of the invention using any transfection method known to those in the art. 24 hours after transfection, the cells may be washed and fresh growth medium added. 48 hours after transfection, the cells may be split into fresh growth medium such that they are no more than 25% confluent. If the cells are too dense, the antibiotic will not kill the cells. Antibiotics work best on actively dividing cells. The cells may be incubated at 37° C. for 2-3 hours until they have attached to the culture dish. The growth medium may be removed and replaced with fresh growth medium containing the Geneticin® at the pre-determined concentration required the particular cell line. The cells may be fed with selective media every 3-4 days until Geneticin®-resistant colonies can be identified. Multiple (e.g., five or more) Geneticin®-resistant colonies can be picked and expanded to assay.
Any suitable assay may be used to detect the activity of the polypeptide having a detectable activity. One suitable assay is described below for the case when the polypeptide has β-lactamase activity.
In some embodiments, polypeptides having a detectable activity according to the present invention may have a β-lactamase activity. β-lactamase activity may be detected using any technique known to those skilled in the art. Kits for the detection of β-lactamase activity are commercially available, for example, GeneBLAzer™ Detection Kits from Invitrogen Corporation, Carlsbad, Calif.
Materials and methods of the invention facilitate fluorescent detection of β-lactamase reporter activity in host cells (e.g., mammalian cells). In one aspect, materials of the invention may include one or more polypeptides having β-lactamase activity as described above. Such polypeptides can be used as reporters of promoter activity or gene expression in mammalian cells, respectively. Materials of the invention may also include one or more fluorescence resonance energy transfer (FRET)-enabled substrates (e.g., CCF2), which facilitate fluorescent detection of β-lactamase reporter activity. In the absence or presence of β-lactamase reporter activity, cells loaded with the CCF2 substrate fluoresce green or blue, respectively. Comparing the ratio of blue to green fluorescence in a population of live cells or in a cell extract of a sample to a negative control provides a means to quantitate gene expression.
In one embodiment of the invention, methods of the invention may employ one or more substrates to detect β-lactamase activity. One example of a suitable substrate for use in methods of the invention is CCF2. CCF2 consists of a cephalosporin core linked to two fluorophores, 7-hydroxycoumarin and fluorescein. In the absence of β-lactamase reporter activity, the substrate molecule remains intact. Excitation of the coumarin at 409 nm results in fluorescence resonance energy transfer (FRET) to the fluorescein moiety. This energy transfer causes the fluorescein to emit a green fluorescence signal with an emission peak of 520 nm. In the presence of β-lactamase reporter activity, the CCF2 substrate is cleaved, disrupting FRET. In this case, excitation of the coumarin at 409 nm results in emission of a blue fluorescence signal with an emission peak of 447 nm. In a population of cells loaded with CCF2 substrate, those that fluoresce blue contain β-lactamase reporter activity while those that fluoresce green do not.
Two derivatives of CCF2 have been developed to enable use of the fluorescent substrate for in vivo or in vitro applications. CCF2-FA may be used for the in vitro detection of β-lactamase activity while CCF2-AM may be used for in vivo detection of β-lactamase activity. CCF2-FA is the free acid form of the CCF2 substrate. This free acid form is water soluble, making it suitable for direct addition to cell lysates. CCF2-AM is a hydrophobic, membrane-permeable, esterified form of the CCF2 substrate. This esterified form is non-toxic, lipophilic and readily enters the cell. Once inside the cell, the CCF2-AM is converted into CCF2.
When added to mammalian cells, the lipophilic, esterified CCF2-AM substrate enters the cell via diffusion, where it is cleaved by endogenous cytoplasmic esterases and rapidly converted into its negatively charged form, CCF2 (see
In one aspect, the present invention provides methods of detecting β-lactamase activity in a lysate prepared from a cell. Such methods may entail preparing a cell lysate from cells of interest using a method that preserves the enzymatic activity of β-lactamase, contacting the lysate with a fluorescent substrate and detecting a change in the fluorescence. A stock of fluorescent substrate (e.g., 100 μM CCF2-FA) can be prepared and the appropriate amount of CCF2-FA can be added to the cell lysate. CCF2-FA fluorescence signal may be detected using a fluorescence plate reader or fluorometer.
In another aspect, the present invention provides methods of detecting β-lactamase activity in a living cell. Such methods may entail introducing into the cells a fluorescence substrate for β-lactamase and detecting a change in the fluorescence of the substrate. Detection of the fluorescence signal may be by any means known in the art (e.g., fluorescence microscopy, ratiometric imaging, fluorescence plate reader, FACS).
A nucleic acid molecule of the invention may be prepared and introduced into a host cell as described above. To perform an in vitro assay for β-lactamase activity in a cell lysate, any suitable method of preparing a lysate may be use. A suitable method is one in which the enzymatic activity of β-lactamase is preserved. An example of a suitable protocol is provided below.
Adherent cells may be harvested by dissociating cells with an EDTA-containing buffer using standard methods (e.g. Versene). Cells may then be counted using a cell counter or a hemacytometer and centrifuged. The cell pellet may be washed twice with HBSS or HBS and resuspended in Hank's Balanced Salt Solution (HBSS) or hepes buffered saline (HBS) to a density of 1×107 cells/ml in a microcentrifuge tube. Trypsin-EDTA should not be used to dissociate the cells as over trypsinizing cells may reduce β-lactamase activity by causing cell lysis and proteolysis. For suspension cells, an aliquot may be counted using a cell counter or a hemacytometer. Cells may be harvested by centrifugation and resuspend in HBSS or HBS to a density of 1×107 cells/ml in a microcentrifuge tube.
Cells prepared as described may be frozen in liquid nitrogen or a dry ice/ethanol bath. The tube may then be transferred to a 30° C. water bath until cells are thawed. To prevent degradation, avoid excessive incubation at 30° C. The cells may be frozen and thawed and additional two times making a total of three freeze thaw cycles.
The cells may then be centrifuge the sample in a microcentrifuge at +4° C. at maximum speed to pellet cell debris. The supernatant may be transferred to a sterile microcentrifuge tube. The cell lysate may be stored at −20° C. or at −80° C. Other suitable methods of preparing a cell lysate are known to those skilled in the art. For example, cell lysates can be prepared using sonication or a gentle detergent such as 1% NP-40, 1% IGEPAL CA-630 (Sigma, Catalog no. 1-3021) or 0.5% CHAPS, if desired. For high-throughput applications, cell lysates may be prepared using one of the detergents suggested above. Cells may be lysed directly in the tissue culture well.
A stock solution of 100 μM CCF2-FA may be prepared in Hank's Balanced Salt Solution (HBSS) or HEPES Buffer Saline (HBS). Other phosphate-based buffers such as Phosphate-Buffered Saline (PBS) are also suitable. Aliquot desired volumes into cryovials and freeze quickly by placing the vials on dry ice or in liquid nitrogen. This minimizes freeze/thaw cycles during use. Once the solutions are frozen, transfer the cryovials to a −20° C. freezer. Store the solutions protected from light. When stored under these conditions, the aqueous CCF2-FA stock solution is stable for at least one month.
A suitable protocol for use in a 96 well plate format is as follows. An aliquot of a cell lysate is added to a well of a 96-well plate. To each well containing sample, CCF2-FA stock solution may be added to obtain a final concentration of 10 μM (10-fold dilution). For example, add 10 μl of CCF2-FA to 90 μl of cell lysate (total volume=100 μl). Proceed to read the fluorescence signal in a fluorescence plate reader or fluorometer. Although β-lactamase cleaves the CCF2 substrate rapidly, longer incubation times may be required to optimize the fluorescence signal when low levels of the enzyme are present in the cell lysate. For example, the fluorescence signal can be read every 15 minutes for 1 hour.
To detect β-lactamase reporter activity in live cells, the CCF2-AM substrate may be used. CCF2-AM is the membrane-permeable, esterified form of CCF2, and is recommended for in vivo use because it is lipophilic and readily enters the cell. Once cells are “loaded” with CCF2-AM, CCF2 fluorescence signal may be quantified using a variety of methods.
A number of factors can influence the degree of cell loading, and consequently, the success of detection. These factors include: the cell type or cell line used; the density of cells at the time of loading; the temperature at which the cells are loaded; the degree to which the cell line retains the CCF2-AM substrate; and the loading protocol used.
Any suitable cell line may be used in the practice of the methods of the invention. For example, any mammalian cell line or cell type of choice may be used to express a β-lactamase reporter construct for detection using methods of the invention. This includes cell lines that grow in suspension or as adherent monolayers. Cell lines may vary significantly in their rate and ability to load and retain the CCF2-AM substrate. A suitable general protocol is provided below. One skilled in the art can optimize the protocol far any particular cell line by varying one or more of the factors described above.
Suspension cells are typically loaded at a density of 1-2×106 cells/ml. Adherent cells load with CCF2-AM substrate most efficiently when they are 60-80% confluent at the time of loading. In contrast, confluent cells load poorly. For analysis of gene expression from a stable cell line, cells may be plated such that they will be 60-80% confluent at the time of loading. For transient analysis of gene expression, cells may be transfected using Lipofectamine™ 2000 Reagent available from Invitrogen Corporation, Carlsbad, Calif. (Catalog no. 11668-027) as recommended by the manufacturer (i.e. 90% confluence for 4-6 hours). Cells may then be incubated cells at 37° C. overnight, then trypsinized and re-plated such that the transfected cells are 50-60% confluent. The cells may then be incubated overnight at 37° C., and loaded the next day.
The rate at which cells load with CCF2-AM substrate is affected by temperature. Generally, increasing the temperature (e.g. from room temperature to 37° C.) will increase the loading rate. However, increasing the temperature also increases the rate at which the substrate is exported from the cell, which may result in lower overall steady-state uptake of CCF2-AM. Cells may be loaded at room temperature.
Cells may be loaded for one hour. Cell lines vary in their ability to load and retain the CCF2-AM substrate. For example, lymphoma cells tend to load in 15-30 minutes, while most adherent cells load well in 30 minutes to 1 hour at room temperature. Generally, fluorescence signal is detectable by 15 minutes after loading and increases steadily for about 60 minutes. Longer incubation times may further increase the intensity of the fluorescence signal, but the increase in intensity is smaller than that observed in the first hour. Depending on the cell line and the application, the CCF2-AM loading time can be varied to optimize the fluorescence signal. One skilled in the art can readily optimize loading time using routine experimentation. For example, cell loading may be visualized using a fluorescence microscope (e.g. take a reading every 15 minutes for up to 2 hours) to determining how quickly the cells fluoresce green. Alternatively, loading may be monitored using a bottom-read fluorescence plate reader (e.g. Gemini-EM Fluorescence Microtiter Plate Reader, Molecular Devices or CytoFluor® 4000 Fluorescence Plate Reader, PerSeptive Biosystems).
Two loading protocols are provided below to facilitate cell loading of CCF2-AM, a General Loading Protocol and an Enhanced Loading Protocol. For most cell lines, the General Loading Protocol is recommended and results in efficient cell loading and a highly detectable CCF2-AM fluorescence signal. In some cell lines, using the General Loading Protocol results in a weak fluorescence signal. These cell lines are generally those that possess active anion transport, resulting in export of the substrate (see examples below). For these cell lines, cells may be loaded using the Enhanced Loading Protocol. Depending on the nature of the cell line, the loading protocol can be varied. Examples of cells that may be loaded using the General Loading Protocol include, but are not limited to, HEK293, COS-7, and Jurkat. Examples of cells that may be loaded using the Enhanced Loading Protocol include, but are not limited to, CHO-K1, CV-1, ME-180, and HepG2.
Once cells have been loaded with the CCF2-AM substrate, a variety of methods can be used to analyze the fluorescence signal including, but not limited to visual inspection of fluorescent cells using fluorescence microscopy, quantitative analysis of blue and green fluorescence by ratiometric imaging using a fluorescence microscope, quantitative analysis of blue and green fluorescence using a fluorescence plate reader, fluorescence-activated cell sorting (FACS) to isolate cells expressing β-lactamase.
A 1 mM stock solution of CCF2-AM in anhydrous DMSO is called Solution A. Solution A can be stored at −20° C., desiccated and protected from light. When stored under these conditions, Solution A is stable for at least one month. Before each use, let the frozen Solution A warm to room temperature and remove the desired amount of reagent. Immediately recap the vial to reduce moisture uptake and return to −20° C. storage. Once thawed, Solution A may appear slightly yellow. This color change is normal and does not affect the performance of the reagent.
In some embodiments, the present invention provides methods of detecting reporter activity in a cell by loading the cell with a fluorescent substrate and detecting a change in the fluorescence of the substrate. For example, methods of the invention may be used to detect β-lactamase reporter activity in a cell line of interest by loading the cells with the fluorescent CCF2-AM substrate and evaluating the difference in blue and green signal intensity compared to a negative control (cells with no β-lactamase reporter activity). Fluorescent substrate may be loaded into the cells with a 6×CCF2-AM Loading Solution using the General Loading Protocol.
In some embodiments, β-lactamase reporter activity may be detected by introducing a fluorescent substrate for β-lactamase activity into one or more cells, and evaluating blue and/or green fluorescence intensity. For example, the fluorescent CCF2-AM substrate may be introduced into cells and the difference in blue and green signal intensity may be evaluated, for example, compared to a negative control (cells with no β-lactamase reporter activity). In some embodiments, the cells may be adherent cells. In other embodiments, the cells may be suspension cells.
In some methods of the invention, after evaluating blue and/or green fluorescence intensity, the cells may be further cultured. Optionally, cells with a desired activity or activity level (e.g., expressing β-lactamase, expressing β-lactamase at a high level, or not expressing β-lactamase) may be separated from cells not having the desired activity or activity level (e.g., by FACS) and cells having desired activity and/or activity levels may be further cultured. In embodiments of this type, sterility may be maintained throughout the experiment, for example, by performing all manipulations within a tissue-culture hood and preparing solutions using sterile reagents.
In some methods of the invention, a fluorescent substrate may be introduced into one or more cells. For example, 6 μl of Solution A may be added to 54 μl of Solution B (100 mg/ml Pluronic®-F127 surfactant in DMSO and 0.1% acetic acid) and vortexed to mix thoroughly. If Solution B is stored at cooler temperatures, a white precipitate may form or the solution may freeze. Warm and mix the solution at 37° C. until the precipitate dissolves. To the mixture, 940 μl of Solution C (24% (w/v) PEG 400, 18% (v/v) TR40 in water) or 940 μl of HBSS can be added to the combined Solutions A and B (60 μl volume) to obtain a final volume of 1 ml. The combined solutions may be vortexed to mix thoroughly. The combined solutions should be used within two hours of preparation as the substrate degrades over time in aqueous solution. This solution is referred to as 6×CCF2-AM Loading Solution.
Solution C is added to reduce non-specific fluorescence due to substrate that has not entered the cell. The presence of Solution C will interfere with the fluorescence signal if fluorescence signal is to be determined using a top-read fluorescence plate reader or by fluorescence-activated-cell sorting (FACS). In embodiments, using these two techniques, 940 μl of HBSS or PBS (Ca2+- and Mg2+-free) may be substituted for Solution C. After loading, remove the loading solution and wash the cells with HBSS. Replace with an equal volume of HBSS before taking a reading (if using a fluorescence plate reader) or prepare cells for flow cytometry (if performing FACS). Reading fluorescence signal from a bottom-read fluorescence plate reader provides the best sensitivity.
The following conditions may be used in connection with methods of the invention. When cells to be used are grown in tissue culture plates, any size tissue culture plate may be used (e.g., 96-well format). Tissue culture plates should be selected to be compatible with the detection instrument to be used. When 96-well plates are to be used, black-walled, clear bottom 96-well plates may be used. Adherent cells may be 60-80% confluent at the time of loading and suspension cells may be loaded at a density of 1-2×106 cells/ml. Cells may be loaded at room temperature. Cells may be loaded for varying amounts of time, for example, from about 10 minutes to about 3 hours, from about 20 minutes to about 2 hours, from about 30 minutes to 1.5 hours, or about 1 hour. Cells may be loaded in HBSS or HBS. Cells may also be loaded in serum-containing media, however, CCF2-AM may hydrolyze during prolonged exposure to serum. This may affect the rate of CCF2-AM loading.
For methods involving loading adherent cells, the following protocol for introducing fluorescent substrate into cells may be use. Cells may be plated in any tissue culture format of choice. Methods may include the use of a negative control (no cells), an untransfected control, and/or an uninduced control to determine the background blue and green fluorescence. Methods of the invention may entail removing the growth medium from the cells and adding the appropriate amount of HBSS to each well and adding a solution comprising the fluorescent substrate. Optionally, cells may be washed one or more times with HBBS before adding HBBS and substrate. Typically, the amount of HBBS added to the cells is greater than the amount of solution comprising substrate added. For example, 5 parts HBBS may be added for 1 part solution comprising substrate may be added to the cells. Examples of suitable amounts of solution comprising substrate and EBBS for various tissue culture dishes are as follows: for a 96-well plate 20 μl substrate and 100 μl HBBS; for a 48-well plate 40 μl substrate and 200 μl HBBS; for a 24-well plate 100 μl substrate and 500 μl HBBS; for a 12-well plate 150 substrate and 750 μl HBBS; and for a 6-well plate 250 μl substrate and 1250 μl HBBS. The final solution comprising HBBS and substrate may contain from about 100 μM substrate to about 5 mM substrate, from about 250 μM substrate to about 2.5 mM substrate, from about 0.5 mM substrate to about 2 mM substrate, or about 1 mM substrate. After substrate and HBBS have been added, plates may be covered to prevent the solution from evaporating. Plates may be incubated for a suitable time at a suitable temperature. Suitable times are from about 5 minutes to about 5 hours, from about 10 minutes to about 4 hours, from about 20 minutes to about 3 hours, from about 30 to about 2.5 hours, from about 45 minutes to about 2 hours, or about 1 hour. A suitable temperature is one from about 4° C. to about 42° C., from about 10° C. to about 37° C., from about 15° C. to about 30° C., or about room temperature. During incubation, cells may be protected from light. As will be appreciated by those skilled in the art, extending the incubation time may increase the fluorescence signal, but may also increase the background. An optimum time may be determined using routine experimentation. After the cells are loaded, fluorescence may be determined using any technique know in the art. Alternatively, cells may be removed from the loading solution, washed and cultured in any appropriate medium until fluorescence is to be determined.
Methods of the invention may entail introducing a fluorescent substrate into suspension cells. Methods may include the use of a negative control (no cells), an untransfected control, and/or an uninduced control to determine the background blue and green fluorescence. Methods of the invention may entail pelleting a suitable number of cells (e.g., 1-2×105 cells) by centrifugation for each suspension culture to be tested. The pelleted cells may be washed one or more times with a suitable medium, for example, HBSS, and then may be resuspended in a suitable volume of a suitable medium (e.g., 100 μl of HBSS). A solution comprising a fluorescent substrate may be added to the re-suspended cells, for example, to a 100 μl sample, 20 μl of the 6×CCF2-AM Loading Solution may be loaded to obtain a final concentration of 1×. Cells in loading solution may be transferred to a black-walled, clear bottom 96-well tissue culture plate. The plate may be covered to prevent the solution from evaporating. Concentrations of fluorescent substrate, incubation times and temperatures may be the same for suspension cells as those set forth above for adherent cells. During incubation, cells may be protected from the light. An optimum time may be determined using routine experimentation. After the cells are loaded, fluorescence may be determined using any technique know in the art. Alternatively, cells may be removed from the loading solution, washed and cultured in any appropriate medium until fluorescence is to be determined. During the incubation, cells will settle to the bottom of the well. If a bottom-read fluorescence plate reader is to be used to determine fluorescence, the plate should be handled gently as the cells must remain at the bottom of each well for accurate detection to occur. The bottom of the plate should not be touched.
After loading cells (adherent or suspension) with the substrate, cells may be inspected visually (e.g., in a fluorescence microscope) to qualitatively assess the fluorescence signal. If the blue and green fluorescence signal is detectable, the cells may be further processed to quantify the reporter activity and/or to select cells with the desired activity and/or activity level. For example, β-lactamase reporter activity may be quantified in live cells using a suitable technique (e.g., a fluorescence plate reader or ratiometric imaging with a fluorescence microscope). If a fluorescence plate reader is used to detect fluorescence signal in whole cells, note that optimal sensitivity is obtained with a bottom-read fluorescence plate reader. Alternatively, cell lysates can be prepared and used to measure β-lactamase reporter activity using a fluorescence plate reader. In some embodiments, FACS may be used to select cells based on their β-lactamase reporter activity.
As will be appreciated in the art, some cell lines take up fluorescent substrate better than other cell lines. To use methods of the invention with cell lines that take up less substrate than desired, methods of the invention may be modified to enhance substrate uptake. For example, for cells that display weak fluorescence signal (i.e. poor substrate retention) by visual inspection on a fluorescence microscope after being loaded as described above, a different loading solution (e.g., 6×CCF2-AM Enhanced Loading Solution) may be used. Cell lines that typically exhibit an increased fluorescence signal after being loaded with the 6×CCF2-AM Enhanced Loading Solution may be those that possess active ion transport mechanisms including, but not limited to, CHO-K1, CV-1, ME-180, and HepG2.
To enhance substrate uptake, cells may be incubated in a solution comprising a higher concentration of substrate (e.g., CCF2-AM). Solutions may also comprise a non-specific inhibitor of anion transport (e.g., probenecid, see DiVirgilio, et al., (1988) J. Immunol. 140, 915-920). Probenecid (p-[Dipropylsulfamoyl]benzoic acid) is available from Sigma (Catalog no. P-8761). Although the presence of probenecid can increase the amount of substrate retained in the cell, it may be toxic to some cell types. If toxicity is observed upon using loading solutions containing probenecid, omit the probenecid.
A probenecid stock solution may be prepared. For example, a 500 mM stock solution may be prepared by dissolving the appropriate amount of probenecid in 0.5 M NaOH. To prepare a 250 mM stock solution (100×), equal volumes of 500 mM stock solution and 100 mM phosphate buffer pH 8.0 may be mixed and the pH of the resulting 250 mM solution may be adjusted to pH 8.0 with 1 M HCl or 1 M NaOH. Aliquots of the 250 mM probenecid stock solution (100×) may be placed in 1 ml microcentrifuge tubes and stored at −20° C. The solution is stable for at least 4 months.
One suitable solution for enhanced uptake of substrate into cells (e.g., 6×CCF2-AM Enhanced Loading Solution) may be prepared using the following protocol. 12 μl of Solution A may be added to 48 μl of Solution B and vortex. If Solution B is stored at cooler temperatures, a white precipitate may form or the solution may freeze. Warm and mix the solution at 37° C. until the precipitate dissolves. Optionally, 60 μl of probenecid 250 mM stock solution can be added to the combined Solutions A and B (total volume=120 μl). 880 μl of Solution C (940 μl if probenecid is omitted) may be added to the loading buffer to obtain a final volume of 1 ml and vortexed to mix.
Enhanced loading solutions should be used within two hours of preparation as the substrate degrades over time in aqueous solution. Discard any unused solution.
In some embodiments, methods of the invention may entail the use of an enhanced loading solution for the introduction of a fluorescent substrate into a cell. In some embodiments, the cells to be loaded using an enhanced loading solution may be adherent cells. Adherent cells may be plated in any tissue culture format of choice. Methods of the invention may include a negative control (no cells), an uninduced control, and/or an untransfected control to determine the background blue and green fluorescence. Methods of the invention may entail removing the growth medium from the cells and washing the cells once with HBSS. An appropriate amount of HBSS may be added to each well. An appropriate amount of an enhanced loading solution (e.g., 6×CCF2-AM Enhanced Loading Solution in a 6-fold dilution) may be added to the well to obtain a suitable final concentration of substrate (e.g., 2 μM CCF2-AM). The plate may be covered to prevent the solution from evaporating. Incubate the cells at a suitable temperature for a suitable time protected from light. Suitable reagent volumes for tissue culture plate type and times and temperatures of incubation include those set out above for loading adherent cells with a fluorescent substrate. Extending the incubation time may increase the fluorescence signal, but may also increase the background. After incubation, fluorescence signal may be detected using the method of choice. Alternatively, the enhanced loading medium may be removed and replaced with fresh, growth medium (optionally containing 1% probenecid stock) or HBSS (optionally containing 1% probenecid stock) and cultured until fluorescence is detected.
In some embodiments, methods of the invention may comprise the use of an enhanced loading solution to load a fluorescent substrate into a cell. Methods of the invention may include a negative control (no cells), an uninduced control, and/or an untransfected control to determine the background blue and green fluorescence. Methods may comprise pelleting 1-2×105 cells by centrifugation for each suspension culture to be assayed. The cell pellet may be washed once with HBSS, then resuspended in 100 μl of HBSS. 20 μl of an enhanced loading solution (e.g., 6×CCF2-AM Enhanced Loading Solution) may be added to 100 μl of cells in buffer to obtain a final concentration of 1× enhanced loading solution. A 1× enhanced loading solution may comprise a greater concentration of fluorescent substrate than other loading solutions (e.g., 2 μM CCF2-AM). Cells in enhanced loading solution may be transferred to a black-walled, clear bottom 96-well tissue culture plate. The plate may be covered to prevent the solution from evaporating. Suitable times and temperatures of incubation include those set out above for loading adherent cells with a fluorescent substrate. Extending the incubation time may increase the fluorescence signal, but may also increase the background. After incubation, fluorescence signal may be detected using the method of choice. Alternatively, the enhanced loading medium may be removed and replaced with fresh, growth medium (optionally containing 1% probenecid stock) or HBSS (optionally containing 1% probenecid stock) and cultured until fluorescence is detected.
Once the cells (adherent or suspension) have been loaded with fluorescent substrate using any on the methods described herein, the fluorescence signal of the substrate (e.g., CCF2) and its β-lactamase-catalyzed hydrolysis product may be detected in cells using any type of fluorescence microscope with a long-pass dichroic mirror to separate excitation and emission light. The dichroic mirror should be matched to the excitation filter to maximally block the excitation light around 405 nm, yet allow good transmission of the emitted light.
Use of the best filter sets will ensure that the optimal regions of the β-lactamase spectra are excited and passed (emitted). To visually inspect the cells, a long-pass filter passing blue and green fluorescence light may be used so that it is possible to visually identify whether the cells are fluorescing blue or green. Suitable filters sets are commercially available, for example, from Chroma Technologies, Rockingham, Vt. or Omega Optical, Brattleboro, Vt. as specified below. FITC filters should not be used. Most FITC filters block emission of blue light so all cells (even those that contain β-lactamase) will appear green. As will be appreciated by one skilled in the art, when the polypeptide having a detectable activity has a β-lactamase activity and the fluorescent substrate used is CCF2 or a derivative thereof, wild-type cells that do not contain the bla(M) reporter gene and possess no β-lactamase activity will emit a green fluorescence signal, while those that contain the bla(M) reporter gene and are expressing β-lactamase will emit a blue fluorescence signal.
Methods of the invention may optionally comprise taking photographs of the cells. A color camera that is compatible with the microscope may be used to photograph the cells. Suitable cameras include digital cameras or cameras using a high sensitivity film, such as 400 ASA or greater.
Methods of the invention may comprise monitoring a detectable activity (e.g., β-lactamase activity) in single cells over time. Such methods may comprise the use of microscopic imaging and ratiometric analysis. For methods comprising microscope-based ratiometric analysis, the blue and green fluorescence emissions are analyzed separately by filtering the emitted light through two emission filters, passing either blue or green fluorescence (analogous to using a fluorescence plate reader). By calculating the ratio of blue to green fluorescence intensities, it is possible to numerically analyze β-lactamase activity. To perform ratiometric analysis, a filter set containing separate blue and green emission filters may be used. Suitable filter sets are commercially available from, for example, Chroma Technologies or Omega Optical as specified below.
Those skilled in the art will appreciate that, as with other fluorescent dyes, photo-bleaching the dye-loaded cells may be avoided. The CCF2 substrate is particularly sensitive to continuous illumination through a high magnification, high numerical aperture objective with UV or any other wavelength of light that can excite the dye. Continuous excitation of the dye can cause the acceptor fluorophore to be bleached (destroyed) with loss of FRET and appearance of donor fluorescence. This effect is progressive and nonreversible.
To reduce photo-bleaching, limit exposure of cells to excitation light by analyzing fluorescence signal for a few seconds at a time. Alternatively, use a lower magnification objective to reduce exposure of the substrate to light.
In some methods of the invention, detectable activity (e.g., β-lactamase activity) may be detected in cells using a fluorescence plate reader. Methods include, but are not limited to, measuring the fluorescence intensity in cell lysates containing fluorescent substrate (e.g., CCF2-FA); measuring the fluorescence intensity in live cells containing fluorescent substrate (e.g., CCF2-AM-loaded cells); and/or lysing the fluorescent-substrate-loaded cells (e.g., CCF2-AM-loaded cells) and measuring fluorescence intensity in cell lysates. The last method may provide better sensitivity if using a top-read fluorescence plate reader.
Any fluorescence plate reader may be used to practice one or more of the methods of the invention. In some embodiments, a bottom-read fluorescence plate reader may be used. Such readers are well know in the art and are commercially available (e.g. Gemini-EM Fluorescence Microtiter Plate Reader, Molecular Devices, CytoFluor® 4000 Fluorescence Plate Reader, PerSeptive Biosystems, or Safire Microplate Reader, Tecan). Top-read fluorescence plate readers (e.g. Gemini-XS Fluorescence Microtiter Plate Reader, Molecular Devices) can be used, however, lower sensitivity may be observed and extra manipulation steps are required before fluorescence signal can be measured in live cells.
Use the optimal filter set to detect ratiometric blue and green readout. Filter sets are included with some fluorescence plate readers, while others require that filters be obtained separately. Filters may be obtained separately, for example, from Chroma Technologies. One suitable filter set is
In the practice of methods of the invention, cells may be plated in any size tissue culture format of choice. One skilled in the art will appreciate the necessity of ensuring that the fluorescence plate reader to be used can accommodate the plate format selected.
In methods that comprise assaying for β-lactamase activity in a 96-well format, cells may be plated in a black-walled, clear-bottom microplate with low autofluorescence (Costar, Catalog no. #3603). Using a black-walled microplate blocks any signal from adjoining wells during reading. For larger-sized tissue culture formats, use of clear tissue culture plates is acceptable.
Those skilled in the art are aware that some plates/plate readers exhibit edge effects that may affect data. If edge effects are noticed, consider the plate layout when setting up the assay.
The bottom of the microtiter plate should not be touched nor should dust be allowed to cover the tissue culture surface. Fingerprints and dust can autofluoresce, introducing well-to-well variability in replicate wells.
Methods of the invention will typically include negative controls (e.g., loading buffer with no cells, cells with no β-lactamase activity, etc.) to determine the background blue and green fluorescence.
Methods of the invention may be practiced using a top-read fluorescence plate reader. In methods involving the quantitating of a fluorescent substrate (e.g., CCF2-AM) fluorescence signal in live cells using a top-read fluorescence plate reader, the dyes from Solution C in the 6×CCF2-AM Loading Solution will interfere with the fluorescence signal. In addition, some components of cell culture media may also interfere with the fluorescence signal. Thus, in methods of this type, the loading solution (e.g., the 6×CCF2-AM Loading Solution) and any cell culture media should be removed from the cells prior to determining fluorescence. For example, cells may be loaded as described above. After loading, the loading solution may be removed and the cells may be washed (e.g., with HBSS). An appropriate amount of HBSS may then be added to the well and the fluorescence signal determined using the top-read fluorescence plate reader. In some embodiments, for example, those in which the cells are not going to be cultured after fluorescence determination, cells may be lysed and then the fluorescence signal determined in the cell lysate as described above. In embodiments where the cells are to be cultured after determination of the fluorescence signal, the HBSS may be removed from the cells and replaced with an appropriate amount of fresh, complete growth media. The cells may then be incubated under appropriate conditions.
In some methods of the invention, it may be desirable to calculate a ratio of blue and green fluorescence intensities. Such a ratio may be calculated by dividing the 460 nm emission (blue channel) reading by the 530 nm emission (green channel) reading. Background fluorescence obtained at each wavelength may be subtracted from the observed emission before the ratio is calculated. Background may be determined by reading one or more of the negative controls (e.g., no cells). Thus, a ratio may be calculated as follows:
The ratio obtained from experimental samples may be compared to the ratio obtained from the appropriate negative controls. One skilled in the art will appreciate that background values are highly dependent on instrument specific factors and on the length of time the lamp in the instrument has been lit. Thus, methods of the invention may comprise determining a background value on each read.
In some methods of the invention, cells may be sorted by FACS after loading with a fluorescent substrate. Any flow cytometer may be used to detect fluorescent-substrate-loaded cells (e.g., CCF2-AM-loaded cells) by flow cytometry. A Krypton laser with violet excitation (407 nm, 413 nm, or multiline violet 407-415 nm) at 60 mW may be used in practice of methods of this type. The flow cytometer may be equipped with the proper optical filters to detect the fluorescence signal from the substrate. When the substrate is CCF2, the fluorescence signal may be detected using HQ460/50m (blue) and HQ535/40m (green) bandpass filters separated by a 490 nm dichroic mirror. Selection of other filter sets suitable for the detection of signals from other fluorescent substrates may be accomplished by one skilled in the art using routine experimentation.
Methods of the invention may comprise aligning and optimizing the instrument to be used. Methods may also entail running a negative control sample (e.g., untransfected or uninduced cells) and a positive control sample to adjust PMT levels and compensation values for optimal separation of the blue and green fluorescence signals. A suitable positive control may be cells expressing the activity to be assayed loaded with a suitable substrate (e.g., cells expressing β-lactamase loaded with CCF2-AM). Other condition for determining fluorescence and sorting cells expressing the desired activity and/or level of activity can be determined by those skilled in the art using routine experimentation.
In methods of the invention that involve sorting of the cells after loading, cells may be loaded as described above except that the loading solution should not contain Solution C. Instead of Solution C the loading buffer may comprise any suitable buffer or medium that does not interfere with the fluorescence detection, for example, HBSS. Cells to be sorted according to the methods of the invention may be suspended in a sorting buffer. Suitable sorting buffers include calcium- and magnesium-free HBSS (Invitrogen Corporation, Carlsbad, Calif., Catalog no. 14175-095) containing 25 mM HEPES (pH 7.3) and 0.1% BSA. In some embodiments, cells to be sorted may be suspended in serum-free medium buffered with 25 mM HEPES (pH 7.3) and 0.1% BSA. This may be useful if cells do not remain sufficiently viable other sorting buffers. Typically, cells are not sorted in tissue culture medium as the buffering capacity is weak and can cause the sample pH to increase in air.
When methods of the invention involve sorting adherent cells, after loading, cells may be removed cells from the tissue culture surface and washed once with a suitable sorting buffer (e.g., calcium- and magnesium-free HBSS). Cells may then be resuspend in sorting buffer at a density of 3−5×106 cells/ml. Cells may be in a single cell suspension.
When methods of the invention involve sorting suspension cells, the cells may be loaded as described above. After loading, cells may be washed with a suitable sorting buffer (e.g., calcium- and magnesium-free HBSS), and resuspended in sorting buffer at a density of 5-10×106 cells/ml.
In methods of the invention that entail cell sorting, cells should be in a single cell suspension during sorting. Formation of aggregates (a major problem with adherent cells) can result in subobtimal sorting due to clogging of the flow cytometer and potential contamination of the sample with unwanted cells. Thus methods of the invention may entail preventing aggregation of cells. Cell aggregation may be prevented by removing divalent metal ions from solutions. Cell aggregation may be prevented by performing all washes with Ca2+- and Mg2+-free solutions, and/or resuspending cells in Ca2+- and Mg2+-free buffers. When methods of the invention involve the use of serum-containing solutions (e.g., if adding serum is added to the cell suspension to preserve cell viability), methods of the invention may entail dialyzing the serum before use to remove Ca2+ and other divalent cations.
Methods of the invention may be optimized using routine experimentation for use with cell types and fluorescent substrates known to those skilled in the art. Factors that may be considered during optimization of the methods disclosed herein may vary with the initial results observed.
In some initial in vitro experiments, a weak fluorescence signal may be observed. This may be the result of low β-lactamase expression. One skilled in the art may consider one or more of the following to optimize the reaction conditions: i) increasing the incubation time of the cell lysate with the fluorescent substrate (e.g., CCF2-FA); ii) re-assessing transfection conditions; and iii) using a different transfection reagent (e.g., Lipofectamine™ 2000 Invitrogen Corporation, Carlsbad, Calif.). A weak fluorescence signal may also result from adherent cells that were dissociated using trypsin-EDTA when preparing a lysate. One skilled in the art may consider using a different dissociation method as over-trypsinizing cells may affect fluorescence signal by causing cell lysis and proteolysis. Versene may be use to dissociate cells. Weak fluorescence signal may also be caused by inefficient cell loading. One skilled in the art might consider in vitro detection of activity. For in vitro detection of β-lactamase, CCF2-FA may be used.
In some initial in vitro experiments, no fluorescence signal may be observed. This may be a result of degradation of the fluorescent substrate. For example, CCF2-FA substrate or stock solution may have been exposed to light during storage or may not have been stored at −20° C. One skilled in the art can readily optimize storage conditions of the substrate, for example, by storing CCF2-FA stock solutions protected from light and at −20° C. Another factor is the method used to prepare the cell lysate, which may have been prepared using a method that destroys the activity of the β-lactamase enzyme. One skilled in the art can adjust the methods used to prepare cell lysates to preserve the activity of the β-lactamase enzyme.
In some initial in vitro experiments, well-to-well variability in replicate wells (most notable when using top-read fluorescence plate readers) may be observed. This may occur if bubbles are present in the cell lysates and may be avoided by carefully transferring cell lysates to a new tissue culture plate, taking care not to introduce bubbles. Variability may also be caused if the bottom of the microtiter plate is touched. The bottom of the microtiter plate should not be touched as fingerprints can autofluoresce. Variability may also be caused when the microtiter plate is covered with dust or lint. Since dust can autofluoresce the bottom and top surface of the microtiter plate should be kept free of dust.
In some initial in vivo experiments, all cells may fluoresce green. This may be caused by poor transfection efficiency. One skilled in the art may consider re-assess transfection conditions and/or using a different transfection reagent (e.g., Lipofectamine™ 2000 Invitrogen Corporation, Carlsbad, Calif.). All cell may fluoresce green if a FITC filter set or other improper filter set is used. One skilled in the art can select a suitable filter set, for example, a filter set that allows both blue (460 nm) and green (520 nm) visualization.
In some initial in vivo experiments, a weak fluorescence signal may be observed. This may be caused by poor substrate retention and corrected by using the enhanced loading methods described herein. Weak fluorescence may be observed if the cells are too dense and may be corrected by plating cells such that they will be 60-80% confluent at the time of loading. Weak fluorescence may be caused by low β-lactamase expression. One skilled in the art might consider i) increasing cell loading time; ii) using the enhanced loading methods described herein; or iii) re-assessing transfection conditions. Weak fluorescence can be caused by loading cell at 37° C. and can be corrected by adjusting the loading temperature (e.g., loading cells at room temperature) Weak fluorescence may be observed if cells were loaded in serum-containing media and may be corrected by loading cells in HBSS or HBS. Weak fluorescence may also be observed if a top-read fluorescence plate reader is used in the presence of media or Solution C and can be corrected by omitting these components or washing the cells to remove them prior to reading.
In some initial in vivo experiments, a hazy background or difficulty visualizing fluorescing cells under the microscope may be observed. This may be caused if cells loaded in the absence of Solution C and may be corrected by adding Solution C to the 6×CCF2-AM Loading Solution.
In some initial in vivo experiments, no fluorescence signal is observed. This may occur if the loading solution is degraded. The loading solution should be used with two hours of making it. This may also be caused by degradation of the fluorescent substrate and corrected by proper storage of the substrate. For example, Solution A should be stored at −20° C., desiccated and protected from light.
In some initial in vivo experiments, cells may detach (in sheets) from the surface of the well. This may be a result of the cell line not being an adherent cell line and may be corrected by plating cells on Matrigel-treated wells. This may also be caused by the cells being sensitive to the surfactant (e.g., from Solution B in the 6×CCF2-AM Loading Solution) and may be corrected by reducing the loading time (e.g. 30 to 45 minutes).
In some initial in vivo experiments, cells exhibit toxicity when loaded using the enhanced loading methods described herein. This may be caused by the probenecid is present in the loading solution and may be corrected by preparing the enhanced loading solution without probenecid and/or loading cells for less time (e.g. 30 to 45 minutes).
In some embodiments, the present invention provides nucleic acid molecules comprising a nucleic acid sequence encoding a polypeptide having a detectable activity. Such nucleic acid molecules may also comprise one or more of features including, but not limited to, recombination sites. One non-limiting example of a nucleic acid molecule of the invention is pcDNA™6.2/GeneBLAzer™-DEST. Nucleic acid molecules of the invention may be used to facilitate in vivo or in vitro detection of β-lactamase reporter activity in cells (e.g., mammalian cells) using a fluorescent substrate. Methods of the invention provide a highly sensitive and accurate method to quantitate gene expression in cells (e.g., mammalian cells).
According to one aspect, nucleic acid molecules of the invention may comprise one or more of the following features: one or more promoters (e.g., human cytomegalovirus immediate-early (CMV) promoter/enhancer for high-level expression in a wide range of mammalian cells, SV40 early promoter, etc.); one or more nucleic acid sequence encoding a polypeptide having a detectable activity (e.g., a nucleic acid sequence encoding β-lactamase bla(M) reporter gene for C-terminal (pcDNA™6.2/cGeneBLAzer™-DEST) or N-terminal (pcDNA™6.2/nGeneBLAzer™-DEST) fusion to the gene of interest); one or more recombination sites (e.g., attR1 and attR2, downstream of the CMV promoter for recombinational cloning of the gene of interest from an entry clone); one or more selectable markers (e.g., the chloramphenicol resistance gene, the blasticidin resistance gene, the spectinomycin resistance gene, the ampicillin resistance gene, any one or more of which may be located between the recombination sites (e.g., attR sites) for counterselection); one or more negative selection markers (e.g., the ccdB gene, which may be located between the two attR sites for negative selection); one or more tag sequences (e.g., the V5 epitope tag for detection using Anti-V5 antibodies); one or more polyadenylation signals (e.g., the Herpes Simplex Virus thymidine kinase polyadenylation signal for proper termination and processing of the recombinant transcript); one or more sequences that permit recovery of single strands (e.g., the f1 intergenic region for production of single-strand DNA in F plasmid-containing E. coli); and one or more origin of replication (e.g., the pUC origin, the SV40 early promoter and origin for expression, which may permit stable propagation of the plasmid in mammalian hosts expressing the SV40 large T antigen, etc.).
A map of pcDNA™6.2/cGeneBLAzer™-DEST and its DNA sequence are provided as
In general, methods of the invention may comprise inserting a sequence of interest into a first nucleic acid molecule of the invention, performing one or more recombination reactions with at least a second nucleic acid molecule of the invention to produce a third nucleic acid molecule of the invention and introducing the third nucleic acid molecule of the invention into one or more host cells. Methods may also include selecting a cell that comprises a nucleic acid molecule of the invention (e.g., a stable cell line). Suitable recombination sites are known to those skilled in the art. Nucleic acid molecules comprising such recombination sites and recombination proteins capable of causing recombination between such sites are commercially available, for example, from Invitrogen Corporation, Carlsbad, Calif. under the trade name of G
Methods of the invention may permit the detection and quantification of gene expression in cells (e.g., mammalian cells). Materials and methods of the invention are suitable for use as a sensitive reporter of gene expression in living mammalian cells using fluorescence microscopy. Materials and methods of the invention provide a ratiometric readout to minimize differences due to variability in cell number, substrate concentration, light intensity, and emission sensitivity. Materials and methods of the invention are compatible with a wide variety of in vivo and in vitro applications including microplate-based transcriptional assays and flow cytometry. Materials and methods of the invention provide a flexible and simple assay development platform for gene expression in cells (e.g., mammalian cells). Materials and methods of the invention typically use a non-toxic substrate that allows continued cell culturing after quantitation analysis.
To join a nucleic acid sequence encoding a polypeptide of interest with a nucleic acid sequence encoding a polypeptide having a detectable activity, a nucleic acid molecule may be constructed in which a sequence encoding a polypeptide of interest is located between two recombination sites that do not recombine with each other. Examples of suitable nucleic acid molecules includes entry vectors available from Invitrogen Corporation, Carlsbad, Calif. Many entry vectors including pENTR/D-TOPO® (Catalog no. K2400-20) are available from Invitrogen to facilitate generation of entry clones.
In some methods of the invention, a fusion protein may be produced. Fusion proteins may be constructed such that one or more stop codons are present in the nucleotide sequence encoding the fusion protein. In some embodiments of the invention such stop codons may be suppressed, for example, by providing a suppressor tRNA that recognizes one or more of the stop codons. Systems to provide such suppressor tRNAs are commercially available, for example, the Tag-On-Demand™ System which allows expression of both native and C-terminally-tagged recombinant protein from the same expression construct is commercially available from Invitrogen Corporation, Carlsbad, Calif.
The Tag-On-Demand™ System is based on stop suppression technology originally developed by RajBhandary and colleagues (see Capone, et al. (1985) EMBO J. 4, 213-221) and comprises a recombinant adenovirus expressing a tRNAser suppressor. When an expression vector encoding a gene of interest with the TAG (amber stop) codon is transfected into mammalian cells, the stop codon will be translated as serine, allowing translation to continue and resulting in production of a C-terminally-tagged fusion protein. For more information, refer to The Tag-On-Demand™ Suppressor Supernatant manual, which is specifically incorporated herein by reference.
In some embodiments, it may be desirable to express a human or mouse gene of interest. Nucleic acid molecules comprising a nucleic acid sequence encoding various human or mouse polypeptides are commercially available, for example, Ultimate™ Human ORF (hORF) or Ultimate™ Mouse ORF (mORF) Clones are available from Invitrogen Corporation, Carlsbad, Calif. Such clones may be fully-sequenced clones provided in a G
In some embodiments, methods of the invention may entail expressing one or more polypeptides of interest from one or more nucleic acid molecules of the invention (e.g., from pcDNA™6.2/cGeneBLAzer™-DEST). A nucleic acid sequence encoding the polypeptide of interest will typically contain a Kozak translation initiation sequence with an ATG initiation codon for proper initiation of translation (see, Kozak, M. (1987) Nucleic Acids Res. 15, 8125-8148, Kozak, M. (1991) J. Cell Biology 115, 887-903, and Kozak, M. (1990) Proc. Natl. Acad. Sci. USA 87, 8301-8305). An example of a Kozak consensus sequence is provided below. The ATG initiation codon is shown underlined.
(G/A)NNATGG
Other sequences are possible, but the G or A at position −3 and the G at position +4 are the most critical for function (shown in bold).
Nucleic acid molecules of the invention (e.g., pcDNA™6.2/cGeneBLAzer™-DEST) may allow expression of recombinant proteins containing a C-terminal β-lactamase reporter. In some embodiments, nucleic acid molecules of the invention may be used to express both a native and a C-terminal fusion protein from the same construct (e.g., by suppression of a stop codon to produce the fusion protein). In embodiments were it is desired to include the β-lactamase reporter fused to a polypeptide of interest, the nucleic acid sequence encoding the polypeptide of interest should contain a Kozak initiation sequence, should not contain a stop codon, and should be in frame with the bla(M) reporter gene after recombination. In embodiments where it is desired to express a native and a C-terminal-fused polypeptide from the same construct (e.g., by suppressing a stop codon), the nucleic acid sequence encoding the polypeptide of interest should contain a Kozak initiation sequence, should contain a stop codon (e.g., TAG), and should be in frame with the bla(M) reporter gene after recombination.
In some embodiments of the invention, materials and methods of the invention may be used to produce a fusion protein in which a polypeptide of interest is fused with a β-lactamase reporter on the N-terminus. Such fusion polypepes may also comprise a tag sequence on the C-terminus. For example, pcDNA™6.2/nGeneBLAzer™-DEST allows expression of recombinant proteins containing an N-terminal β-lactamase reporter and a C-terminal V5 epitope tag, if desired, and contains an ATG initiation codon within the context of a Kozak consensus sequence. This vector may be used in conjunction with the Tag-On-Demand™ System. In embodiments where it is desired to include the β-lactamase reporter, the nucleic acid sequence encoding a polypeptide of interest should not contain a Kozak initiation sequence and should be in frame with the bla(M) reporter gene after recombination. In embodiments where it is desired to include the V5 epitope tag, the sequence encoding a polypeptide of interest should not contain a stop codon and should be in frame with the V5 epitope after recombination. In embodiments where it is desired to include the V5 epitope for use with a suppressor tRNA (e.g., in the Tag-On-Demand™ System), the nucleic acid sequence encoding the polypeptide of interest should contain a stop codon recognized by the suppressor tRNA (e.g., TAG for Tag-On-Demand™), and should be in frame with the V5 epitope after recombination. In embodiments where it is desired to express an N-terminal fusion protein with a native C-terminus, for example to not include the V5 epitope tag when using pcDNA™6.2/nGeneBLAzer™-DEST, the sequence encoding a polypeptide of interest should contain a stop codon.
In general, methods of the invention may comprise performing an LR recombination reaction using the attL-containing entry clone and the attR-containing pcDNA™6.2/GeneBLAzer™-DEST vector; transform the reaction mixture into a suitable E. coli host; and selecting for expression clones.
Some of the nucleic acid molecules of the invention may comprise one or more selectable markers that permit selection against hosts comprising nucleic acid molecules containing the marker. For example, pcDNA™6.2/GeneBLAzer™-DEST vectors contain the ccdB gene. These vectors can be propagated using Library Efficiency® DB3.1™ Competent Cells (Invitrogen Corporation, Carlsbad, Calif., Catalog no. 11782-018). The DB3.1™ E. coli strain is resistant to CcdB effects and can support the propagation of plasmids containing the ccdB gene. General E. coli cloning strains including TOP 10 or DH5α can not be used for propagation and maintenance of the pcDNA™6.2/GeneBLAzer™-DEST vectors as these strains are sensitive to CcdB effects.
The recombination region of the expression clone resulting from pcDNA™6.2/cGeneBLAzer™-DEST×entry clone is shown in
The recombination region of the expression clone resulting from pcDNA™6.2/nGeneBLAzer™-DEST×entry clone is shown in
A nucleic acid molecule containing a nucleic acid sequence encoding a polypeptide of interest located between to recombination sites, (e.g., an entry clone containing a gene of interest between two attR sites), a recombination reaction can be performed (e.g., an LR reaction) between the entry clone and the pcDNA™6.2/GeneBLAzer™-DEST vector, and the reaction mixture can be transformed into a suitable E. coli host to select for an expression clone. A positive control may be included in the experiment, such as pENTR™-gus positive control supplied with the LR C
Some nucleic acid molecules of the invention may contain the EM7 promoter and the Blasticidin resistance gene (e.g., pcDNA™6.2/GeneBLAzer™-DEST vectors). The blasticidin resistance gene allows for selection of E. coli transformants using Blasticidin. For selection, use Low Salt LB agar plates containing 100 μg/ml Blasticidin. For Blasticidin to be active, the salt concentration of the medium must remain low (<90 mM) and the pH must be 7.0. Blasticidin is commercially available, for example, from Invitrogen Corporation, Carlsbad, Calif.
In some embodiments, methods of the invention may be practiced using one or more of the following materials: purified plasmid DNA of an entry clone (50-150 ng/μl in TE, pH 8.0); pcDNA™6.2/cGeneBLAzer™-DEST or pcDNA™6.2/nGeneBLAzer™-DEST vector (150 ng/μl in TE, pH 8.0); LR C
One suitable protocol for carrying out methods of the invention may entail adding the following components to 1.5 ml microcentrifuge tubes at room temperature and mixing.
To include a negative control, a second sample reaction may be prepared omitting the LR C
Methods of the invention may entail removing the LR CLONASE™ enzyme mix from −80° C. and thawing on ice (˜2 minutes); vortexing the LR C
Typically, if E. coli cells with a transformation efficiency of 1×108 cfu/μg are used, the LR reaction should give >5000 colonies if the entire transformation is plated.
The ccdB gene mutates at a very low frequency, resulting in a very low number of false positives. True expression clones will be ampicillin-resistant and chloramphenicol-sensitive. Transformants containing a plasmid with a mutated ccdB gene will be both ampicillin- and chloramphenicol-resistant. To check your putative expression clone, test for growth on LB plates containing 30 μg/ml chloramphenicol. A true expression clone will not grow in the presence of chloramphenicol.
In some embodiments, a nucleic acid molecule comprising a nucleic acid sequence encoding a polypeptide of interest fused to a polypeptide having a detectable activity may be sequenced to ensure that the coding regions of the polypeptide of interest and the polypeptide having a detectable activity are in the same reading frame. For example, to confirm that sequence encoding a polypeptide of interest is in frame with the bla(M) reporter gene, the expression construct may be sequenced. Sequencing primers may be designed such that a forward primer hybridizes within the 3′ end of the sequence encoding a polypeptide of interest to sequence through the attB2 site and the 5′ region of the bla(M) reporter gene for a C-terminal fusion. A reverse primer that hybridizes within the bla(M) reporter gene cannot be used as any primer that hybridizes within the bla(M) reporter gene will also hybridize within the ampicillin resistance gene on the plasmid, contaminating the results. Thus, only the sense strand of an expression construct can be sequenced. The T7 Promoter primer may be used to sequence through the attB 1 site and into the 5′ region of the sequence encoding a polypeptide of interest. Refer to
N-terminal fusion proteins prepared according to one aspect of the invention can be sequenced to confirm that the sequence encoding a polypeptide of interest is in frame with the sequence encoding the bla(M) reporter gene or the V5 epitope tag. Sequencing primers may be designed such that a reverse primer hybridizes within the 5′ end of the sequence encoding the polypeptide of interest to sequence through the attB1 site and the 3′ region of the sequence encoding the bla(M) reporter gene. Forward primers that hybridize within the bla(M) reporter gene cannot be used as any primer that hybridizes within the β-lactamase reporter gene will also hybridize within the ampicillin resistance gene, contaminating the results. Thus, only the anti-sense strand of the expression construct can be sequenced. The TK polyA Reverse primer to sequence can be used to sequence through the attB2 site and into the V5 epitope.
Nucleic acid molecules of the invention may be introduced into host cells (e.g., mammalian cells). For example, nucleic acid molecules in which a nucleic acid sequence encoding a polypeptide of interest is joined to a nucleic acid sequence encoding a polypeptide having a detectable activity such that a fusion polypeptide comprising all or a portion of both polypeptides can be expressed may be introduced into a host cell. Positive control vectors (e.g., pcDNA™6.2/cGeneBLAzer™-GW/lacZ or pcDNA™6.2/nGeneBLAzer™-GW/lacZ) and a mock transfection (negative control) may be included in experiments to evaluate results.
Once expression clone have been generated, plasmid DNA may be isolated for transfection. Plasmid DNA for transfection into eukaryotic cells must be very clean and free from phenol and sodium chloride. Contaminants will kill the cells, and salt will interfere with lipid complexing, decreasing transfection efficiency. Suitable plasmid DNA can be prepared using the S.N.A.P.™ MiniPrep Kit (Invitrogen Corporation, Carlsbad, Calif. 10-15 μg DNA, Catalog no. K1900-01), the S.N.A.P.™ MidiPrep Kit (Invitrogen Corporation, Carlsbad, Calif. 10-200 μg DNA, Catalog no. K1910-01), or CsCl gradient centrifugation.
pcDNA™6.2/cGeneBLAzer™-GW/lacZ or pcDNA™6.2/nGeneBLAzer™-GW/lacZ can be used as positive control vectors for mammalian cell transfection and expression.
Cells may be transfected with the nucleic acid molecules of the invention using any technique known in the art, for example, those described in the preceding example.
Nucleic acid molecules of the invention (e.g., the pcDNA™6.2/GeneBLAzer™-DEST vectors) may contain the Blasticidin resistance gene to allow selection of stable cell lines. To create stable cell lines, transfect the construct into the cell line of choice (e.g., mammalian cell line of choice) and select for foci using Blasticidin.
Nucleic acid molecules of the invention (e.g., pcDNA™6.2/GeneBLAzer™-DEST constructs) may be linearized before transfection. While linearizing the vector may not improve the efficiency of transfection, it increases the chances that the vector does not integrate in a way that disrupts elements necessary for expression in host cells. To linearize the construct, cut at a unique site that is not located within a critical element or within the sequence encoding the polypeptide of interest.
To successfully generate a stable cell line expressing a polypeptide of interest, determine the minimum concentration of Blasticidin required to kill the untransfected host cell line by performing a kill curve experiment. Typically, concentrations ranging from 2.5 to 10 μg/ml Blasticidin are sufficient to kill most untransfected mammalian cell lines. Blasticidin is available separately from Invitrogen Corporation, Carlsbad, Calif. (Catalog no. R210-01). To perform a kill curve experiment, plate cells at approximately 25% confluence. Prepare a set of 6 plates. On the following day, replace the growth medium with fresh growth medium containing varying concentrations of Blasticidin (e.g. 0, 1, 3, 5, 7.5, and 10 μg/ml Blasticidin). Replenish the selective media every 3-4 days, and observe the percentage of surviving cells. Count the number of viable cells at regular intervals to determine the appropriate concentration of Blasticidin that prevents growth within 10-14 days after addition of Blasticidin.
Once the appropriate Blasticidin concentration to use for selection has been determined, stable cell lines can be prepared expressing polypeptides encoded by nucleic acid sequences present on nucleic acid molecules of the invention (e.g., pcDNA™6.2/GeneBLAzer™-DEST constructs).
Methods of preparing a stable cell may comprise transfecting a host cell (e.g., a mammalian cell line of interest) with one or more nucleic acid molecules of the invention (e.g., pcDNA™6.2/cGeneBLAzer™-DEST or pcDNA™6.2/nGeneBLAzer™-DEST expression constructs) using a transfection method of choice. Such methods may further include 24 hours after transfection, washing the cells and adding fresh growth medium; 48 hours after transfection, splitting the cells into fresh growth medium such that they are no more than 25% confluent; incubating the cells at 37° C. for 2-3 hours until they have attached to the culture dish; removing the growth medium and replacing with fresh growth medium containing Blasticidin at the predetermined concentration required for the cell line; feeding the cells with selective media every 3-4 days until Blasticidin-resistant colonies can be identified; and picking at least 5 Blasticidin-resistant colonies and expanding them to assay for recombinant protein expression. Cells should be plated at the indicated degree of confluence. If the cells are too dense, the antibiotic will not kill the cells. Antibiotics work best on actively dividing cells.
Methods of the invention may comprise detecting the presence or absence of a fusion protein by detecting one or more detectable activity. When the detectable activity is β-lactamase reporter activity, it may be detected in vivo or in vitro as described in the preceding example. Fusion polypeptides of the invention may also comprise a tag sequence that may be detected. For example, a polypeptide expressed from a pcDNA™6.2/nGeneBLAzer™-DEST expression construct that contains a sequence encoding a polypeptide of interest fused to the V5 epitope tag may be detected by Western blot analysis using Anti-V5 Antibodies. Suitable antibodies are commercially available, for example, from Invitrogen Corporation, Carlsbad, Calif. Any one of Anti-V5 Antibody (Catalog no. R960-25), Anti-V5-HRP Antibody (Catalog no. R961-25), or Anti-V5-AP Antibody (Catalog no. R962-25) can be used to detect the V5 epitope. In addition, the Positope™ Control Protein (Invitrogen Corporation, Carlsbad, Calif. Catalog no. R900-50) is available for use as a positive control for detection of fusion proteins containing a V5 epitope. The ready-to-use WesternBreeze® Chromogenic Kits and WesternBreeze® Chemiluminescent Kits are available from Invitrogen Corporation, Carlsbad, Calif. to facilitate detection of antibodies by colorimetric or chemiluminescent methods.
Expression of a protein fused to the β-lactamase reporter and/or to the V5 epitope tag will increase the size of the recombinant protein. Below are listed the increase in the molecular weight of a recombinant protein that can be expected from a particular fusion. Note that the expected sizes take into account any additional amino acids between the gene of interest and the fusion peptide.
If lacZ expressing vectors (e.g., pcDNA™6.2/cGeneBLAzer™-GW/lacZ or pcDNA™6.2/nGeneBLAzer™-GW/lacZ) are used as a positive control vectors, β-galactosidase expression can be assayed using techniques well known in the art. For example, β-galactosidase activity may be assayed by Western blot analysis or activity assay (see, Miller, J. H. (1972). Experiments in Molecular Genetics (Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory). Commercially available antibodies and assays may be used. For example, Invitrogen Corporation, Carlsbad, Calif. offers β-Gal Antiserum, the β-Gal Assay Kit, and the β-Gal Staining Kit for fast and easy detection of β-galactosidase expression.
The β-lactamase gene, coupled with the CCF2 or CCF4 substrate, is an excellent reporter system for promoter studies in mammalian cells. A “promoterless” β-lactamase vector (pGeneBlazer,
The β-lactamase reporter system is very versatile, allowing quantitative analyses in either live cells or in cell lysates (making it superior to luciferase or β-galactosidase assays), and the enzymatic nature of β-lactamase makes it more sensitive than GFP (less than 100 molecules of β-lactamase protein per cell are required for detection by eye). Live single cells can be analyzed with the cell-permeable CCF2-AM (or CCF4-AM, described below)) substrate either a) visually (expressing cells fluoresce blue, non-expressing cells fluoresce green), b) quantitatively (on a fluorescence microplate reader) or c) by FACS analysis (including the ability to quantitatively sort expressing cells from non-expressing cells). Alternatively, the CCF2-FA (free acid) form of the substrate can be used directly in traditional cell lysates and quantitated with a fluorescence microplate reader. In all cases, the fact that both the uncatalyzed substrate and the catalyzed product are fluorescent (green and blue, respectively) allows all data to be ratiometric and reported as a blue/green ratio. This automatically minimizes interference from variations in cell size, probe concentration, excitation intensity and emission sensitivity (Zlokarnik et. al. 1998). Maximum excitation of CCF substrates is 409 nm. Green emission is 520 nm and blue emission is 447 nm.
There are currently two versions of the substrate available: CCF2 and CCF4. Functionally both are similar, emitting green fluorescence prior to catalysis by β-lactamase and emitting blue fluorescence after. CCF4 may be more stable in aqueous solution, making it more attractive to large volume high-throughput users. However, for ordinary use CCF2 and CCF4 are indistinguishable.
CCF2 comes in two different forms: CCF2-AM and CCF2-FA. CCF2-AM is the ester form of the substrate, which is hydrophobic and capable of crossing live cell membranes—allowing it to be used in vivo. Once inside the cell, the endogenous cellular esterases remove the ester groups from CCF2-AM making it charged and hydrophilic. This causes the substrate to be trapped inside the cell and results in cells “loading” with more and more substrate over time, increasing the sensitivity of the assay without requiring higher concentrations of substrate. CCF2-FA is the free acid form of the substrate. This is essentially CCF2-AM with the ester groups removed, making it water soluble and appropriate for adding directly to cell lysates for enzymatic studies.
Examples are provided of TOPO-cloning three known mammalian promoters and quantitating their expression levels in whole live cells and in cell lysates.
Materials and Methods:
Cloning β-Lactamase Gene
The β-lactamase gene was generated from the ampR gene in pCMV/myc/nuc, with PCR forward primer 5′-CACCATGGACCCAGAAACGCTGGTGAAAG-3′ and PCR reverse primer 5′-CGATTACTTACCAATGCTTAATCAGTGAGG-3′. PCR amplified product was cloned into pCR-Blunt TOPO vector (Invitrogen Corporation, Carlsbad, Calif.) and sequence confirmed.
Generate pGeneBlazer Vector
The β-lactamase gene was released from pCR-Blunt with EcoRI and EcoRV digestion. Vector backbone was generated from pGlow template (Invitrogen Corporation, Carlsbad, Calif.) with EcoRI and XmaI digestion (to remove GFP and BGHpA). TKpA was generated from pcDNA3.2 (Invitrogen Corporation, Carlsbad, Calif.) with PmeI and XmaI. Expected size fragments from these digestion were purified from 1.2% E-Gel. The purified fragments were ligated and transformed into TOP 10 cells and plated on LB/Amp plates. The cloning junctions were sequence confirmed. The final vector is called pGeneBlazer (
TOPO Charging
Bi-directional TOPO Charging at EcoRI was performed using published protocols (see Heyman, et al. Genome Research 9:383-392 (1999).
Comparison of the Cloning Efficiency of UbC Promoter Vs. 750 bp Test Insert
The UbC promoter was amplified from pUb6/V5HisB (Invitrogen Corporation, Carlsbad, Calif.) template with forward primer 5′-GACGGATCGGGAGATCTGG-3′ and reverse primer 5′-GGTACCAAGCTTCGTCTAAC-3′ (expected size: 1241 bp). The PCR conditions were the same for UbC and the test insert.
For Test Insert, 100 ng Template was Used for PCR
PCR conditions were as follows: 94° C. 2 min (1 cycle); 94° C. 30 sec->55° C. 30 sec->72° C. 60 sec (25 cycles); 72° C. 2 min (1 cycle); and 4° C.
TOPO Cloning reactions contained the following components: PCR product 1 μl; Salt solution 1 μl; TOPO charged Vector: 1 μl, and dH2O: 3 μl.
Two μl of the cloning products were transformed into TOP 10, and 10 μl were plated on LB/Amp plate. As controls, we also transformed PCR products without cloning to check the background from original template.
Cloning CMV, CMV/TetO, and UbC Promoters
CMV, CMV/TetO and UbC promoters were generated by PCR. PCR conditions for the promoters were as following:
PCR reactions were performed as follows: 94° C. 4 min (1 cycle); 94° C. 30 sec->55° C. 30 sec->68° C. 90 sec (30 cycles); 68° C. 10 min (1 cycle); and 4° C. hold.
One microliter of unpurified PCR products was used for TOPO cloning and transformed into TOP 10, plated on LB/Amp plates.
Transfection and Expression in Mammalian Cells
pGeneBlazer/CMV, pGeneBlazer/CMVTetO, pGeneBlazer/UbC were transfected into GripTite 293 cells using the “rapid” 96-well transfection protocol (Lipofectamine2000 Product Manual, Invitrogen Corporation, Carlsbad, Calif.). Briefly, 320 ng of each DNA was diluted into 25 μl OPTI-MEM I in 96-well cell culture plates with black wall and clear bottom (Costar, cat No. 3603). For each well, 0.6 μl of Lipofectamine 2000 was diluted into 25 μl OPTI-MEM I medium and incubated at room temperature for 5 min, then added to the diluted DNA in each well, mixed gently, and incubated at room temperature for 20 min to allow DNA-lipid complexes to form. A GripTite 293 cell suspension was prepared (8.5×105 cells/ml) and 100 μl of cell suspension was added (8.5×104 cells/well) to each of the wells containing the DNA-LF2000 Reagent complexes and mixed gently. The plates were incubated at 37° C., 10% CO2 incubator for 24 hr.
Detection of β-Lactamase Activity
Solution A (1 mM CCF4-AM in dry DMSO) was prepared according to the manufacturer's protocol (PanVera). One ml of 6×CCF4-AM loading solution was prepared by adding 6 μl of Solution A to 60 μl of Solution B (100 mg/ml Pluronic-F127 in DMSO containing 0.1% Acetic Acid) followed by vortexing. Then this combined solution was added to 934 μl Solution C with vortexing, for a final volume of 1 ml. The cells were washed with HBSS, then 100 μl HBSS was added to each well. 20 μl of 6× loading solution was added to the 100 μl of cells in buffer. Cells were incubated at room temperature, protected from light, for 60 minutes (for CCF2-AM) or 90 minutes (for CCF4-AM). Cells were observed under Fluorescence Microscopy equipped with β-lactamase filter (e.g., Omega Filters #XF106-2 excitation: 400DF15, dichroic 420DCLP, emission: 435ALP, or Chroma Filters #41031 excitation: HQ405/20x, dichroic: 425DCXR, emission: HQ430LP) and photographed. Exact excitation of CCF substrates is 409 nm, green emission is 520 nm and blue emission is 447 nm.
After photography, cells were rinsed with PBS and lysed with 60 μl of Tropix lysis solution (0.1 M KCl, 0.2% Triton X-100), fluorescence was measured on a Gemini-XS Fluorescence Microtiter Plate Reader (Molecular Devices) at excitation: 405±10 nm, emission (blue): 460±20 nm, emission (green): 530±15 nm. Cells can also be lysed with 1% NP-40 or 1% IGEPAL CA-630 (Sigma # I-3021) or 0.5% CHAPS or sonicated or freeze/thaw with equivalent results.
The following volumes may be used with the indicated tissue culture plates:
Other volumes may also be used as indicated elsewhere herein.
Activity of β-lactamase can also be measured directly in pre-made cell lysates. For this, CCF2-FA is recommended since it is already de-esterified and readily soluble in aqueous solution. CCF2-FA should be used at a final concentration of 10 μM in lysates. A more detailed protocol for lysate experiments with CCF2-FA can be obtained directly from PanVera.
Results and Discussion:
The β-lactamase gene, when used in mammalian cells, has the first 23 amino acids removed from the bacterial ampicillin gene. This deletes the periplasmic secretion signal without affecting the enzymatic activity. After cloning and sequencing, we identified a silent single point mutation (nucleotide 54 of the ORF, where “A” of the ATG start codon is nucleotide #1) in vectors of the invention that carry a β-lactamase gene derived from Invitrogen's ampR gene. This single nucleotide polymorphism does not change the amino acid sequence.
TOPO Charging and Promoter Cloning
Bi-directional TOPO charging was performed at the EcoRI site. The standard 750 bp “test insert” was PCR amplified with Taq polymerase, as was the UbC promoter. The results of TOPO cloning these two inserts are shown in below. Approximately >95% vectors contained insert.
Expression clones for each promoter (pGeneBlazer/CMV, pGeneBlazer/CMVTetO or pGeneBlazer/UbC) were successfully generated by Topo cloning PCR products of CMV, CMVTetO or UbC. Platinum Hi-Fi was the PCR enzyme used for these reactions. Taq amplification gives higher Topo cloning numbers but has no proof-reading.
Expression and Analysis in Mammalian Cells
GripTite 293 cells were transiently transfected with each of the three promoter expression clones and β-lactamase activity was detected with the CCF4-AM substrate using both fluorescence microscopy and microplate reader quantitation (note that CCF2-AM and CCF4-AM perform equally in these experiments). As controls, the promoterless pGeneBlazer parent vector (supercoiled, no promoter cloned) and promoterless pGlow (Invitrogen Corporation, Carlsbad, Calif., supercoiled, no promoter cloned) were also transfected. Live transfected cells were loaded with CCF4-AM for ninety minutes and fluorescent photographs were taken under the microscope (
Quantification of promoter strength was performed by lysing the CCF4-loaded transfected cells (from
Some β-lactamase activity was observed in cells transfected with the promoterless pGeneBlazer control (compared to the pGlow control, see
The β-lactamase gene, coupled with the CCF2 substrate, is an excellent reporter and detection system for protein expression in mammalian cells (Whitney et al. (1998) Nat. Biotechnol. 16:1329-33; and Zlokarnik, et al. (1998) Science 279:84-88). Destination vectors have been developed for expressing either N- or C-terminal fusions of the β-lactamase ORF with your protein of interest in mammalian cells. These vectors are analogous to the popular mammalian N- and C-terminal GFP fusion vector products except that they are built in the pcDNA6.2 backbone (CMV expression, tk polyA, blasticidin resistance). These new vectors are called pcDNA6.2/nGeneBlazer-DEST and pcDNA6.2/cGeneBlazer-DEST, for N- and C-term β-lactamase fusions, respectively.
The β-lactamase reporter system is very versatile, allowing quantitative analyses in either live cells or in cell lysates (making it superior to luciferase or β-galactosidase assays), and the enzymatic nature of β-lactamase makes it more sensitive than GFP (less than 100 molecules of β-lactamase protein per cell are required for detection by eye; Zlokarnik et. al. 1998). Live single cells can be analyzed with the cell-permeable CCF2-AM substrate (or CCF4-AM, see below) either a) visually (expressing cells fluoresce blue, non-expressing cells fluoresce green), b) quantitatively (on a fluorescence microplate reader) or c) by FACS analysis (including the ability to quantitatively sort expressing cells from non-expressing cells). Alternatively, the CCF2-FA (free acid, see below) form of the substrate can be used directly in traditional cell lysates and quantitated with a fluorescence microplate reader. In all cases, the fact that both the uncatalyzed substrate and the catalyzed product are fluorescent (green and blue, respectively) allows all data to be ratiometric and reported as a blue/green ratio. This automatically minimizes interference from variations in cell size, probe concentration, excitation intensity and emission sensitivity (Zlokarnik et. al. 1998). Maximum excitation of CCF substrates is 409 nm. Green emission is 520 nm and blue emission is 447 nm.
There are currently two versions of the substrate available: CCF2 and CCF4. Functionally both are similar, emitting green fluorescence prior to catalysis by β-lactamase and emitting blue fluorescence after. CCF4 may be more stable in aqueous solution, making it more attractive to large volume high-throughput users. For most applications, however, CCF2 and CCF4 are indistinguishable.
CCF2 comes in two different forms: CCF2-AM and CCF2-FA. CCF2-AM is the ester form of the substrate, which is hydrophobic and capable of crossing live cell membranes—allowing it to be used in vivo. Once inside the cell, the endogenous cellular esterases remove the ester groups from CCF2-AM making it charged and hydrophilic. This causes the substrate to be trapped inside the cell and results in cells “loading” with more and more substrate over time, increasing the sensitivity of the assay without requiring higher concentrations of substrate. CCF2-FA is the free acid form of the substrate. This is essentially CCF2-AM with the ester groups removed, making it water soluble and appropriate for adding directly to cell lysates for enzymatic studies.
Examples are provided of G
Materials and Methods:
Destination Vector Cloning:
Construction of pcDNA6.2/V5-2/FLS-1 (intermediate vector).
The 4685 bp SnaBI/Age I fragment from pcDNA6.2-DEST (Invitrogen Corporation, Carlsbad, Calif.) was ligated with the 455 bp SnaBI/AgeI fragment from pcDNA3.1V5HisA (Invitrogen Corporation, Carlsbad, Calif.) to generate pcDNA6.2-MCS. A 143 bp HindIII/AgeI fragment was removed from pcDNA6.2-MCS and replaced with the synthetic V5-2/FLS-1 polylinker to create pcDNA6.2/V5-2/FLS-1. The sequences of the oligonucleotides forming the V5-2/FLS-1 polylinker were: 5′ AGCTGAGCGCTGTTAACGGGAAGCCTATCCCTAACCC TCTCCTCGGTCTCGATTCTACGCGTA 3′ (sense strand) (SEQ ID NO:121) and 5′ CCGGTACGCGTAGAATCGAGACCGAGGAGAGGGTTAG GGATAGGCTTCCCGTTAACAGCGCTC 3′ (complementary strand) (SEQ ID NO:122). Clones of pcDNA6.2/V5-2/FLS-1 were verified by restriction endonuclease digestion patterns and DNA sequencing analysis.
Construction of pcDNA6.2/nGeneBlazer-DEST
The frame B G
Construction of pcDNA6.2/cGeneBlazer-DEST
The frame B G
Creation of Expression Control Vectors
pcDNA6.2/nGeneBlazer-GW/lacZ was generated by standard G
Both DEST vectors were assayed to measure colony output and to detect ccdB mutants and plasmid contamination.
Expression and Analysis:
GripTite 293, CHO or COS-7 cells were plated in 24-well plates and transiently transfected using Lipofectamine 2000, following the manufacturer's recommended protocol (Invitrogen Corporation, Carlsbad, Calif.). 48 hours post transfection, cells were either 1) labeled with CCF4-AM to detect β-lactamase activity (see protocol below), 2) fixed and stained for β-galactosidase expression using the Beta-galactosidase Staining Kit (Invitrogen Corporation, Carlsbad, Calif.), 3) harvested for Tropix β-galactosidase activity assay (PE Biosystems), or 4) harvested for anti-lacZ western blotting (4-12% NuPage Bis-Tris gel and W
In vivo β-lactamase detection using CCF4-AM was performed as follows. Twenty-four hours post transfection, cells were trypsinized and re-plated into black-walled clear-bottom 96-well plates (Costar #3603) at 4.5×104 cells/well in 100 μl complete media. The following day, cells were loaded by adding 20 μl 6×CCF4-AM loading solution into each well (wells already contain 100 μl complete media and cells, final volume was 120 μl) and incubating for 90 minutes at room temperature. One ml of 6×CCF4-AM loading solution was prepared by adding 12 μl of Solution A (1 mM, CCF4-AM in dry DMSO) to 60 μl of Solution B (100 mg/ml Pluronic-F127 in DMSO containing 0.1% Acetic Acid) followed by vortexing. Then this combined solution was added to 934 μl Solution C with vortexing, for a final volume of 1 ml (final CCF4-AM concentration was 12 μM in the 6× stock, 2 μM final on cells). After 90 minutes loading at room temperature, cells were observed under fluorescence microscopy equipped with β-lactamase filters (e.g., Omega Filters #XF106-2 excitation: 400DF15, dichroic 420DCLP, emission: 435ALP, or Chroma Filters #41031 excitation: HQ405/20x, dichroic: 425DCXR, emission: HQ430LP) and photographed. Exact excitation of CCF substrates is 409 nm, green emission is 520 nm and blue emission is 447 nm.
Results and Discussion:
Destination Vector QC
Vectors pcDNA6.2/nGeneBlazer-DEST and pcDNA6.2/cGeneBlazer-DEST were assayed for colony output and ccdB mutations.
The ccdB assay yielded the following results.
Expression and Analysis in Mammalian Cells
GripTite 293 cells (Invitrogen Corporation, Carlsbad, Calif.) were transiently transfected with each of the fusion controls (pcDNA6.2/nGeneBlazer-GW/lacZ and pcDNA6.2/cGeneBlazer-GW/lacZ), which express the β-lactamase ORF fused to either the N- or C-terminus of the lacZ ORF. Forty-eight hours post transfection, cells were loaded with CCF4-AM (see Materials and Methods) and photographed under fluorescence microscopy (
COS-7 cells were also transiently transfected with each of the fusion expression controls. Forty-eight hours post transfection, cells were lysed and analyzed by either anti-lacZ western blotting (
Compatibility with Tag-on-Demand
The C-terminal GeneBlazer vector (pcDNA6.2/cGeneBlazer-DEST) is compatible with Tag-On-Demand provided that the G
The N-terminal GeneBlazer vector will always express a fusion protein (β-lac/ORF). Fusion to the C-terminal V5 antibody epitope tag requires an ORF with no stop codon. If the ORF contains a TAG stop codon, Tag-On-Demand can be used to express a β-lac/ORF/V5 fusion protein. This may be useful if no convenient antibodies are available for the ORF.
Mammalian GeneBlazer vectors encode the β-lactamase gene for expression and other analyses. The construction of pENTR/GeneBlazer™, a G
Materials and Methods
Cloning of pENTR/GeneBlazer
The β-lactamase gene was amplified using the PCR primers b1β and b2βTAGA and pUC19 as the template. This PCR amplified fragment was reacted with pDONR221 (Invitrogen Corporation, Carlsbad, Calif.) in a BP C
Creation of Expression Control Vectors
pcDNA6.2/FRT/V5-2-GW/GeneBlazer was generated by standard G
Expression and Analysis:
GripTite 293 cells were plated in 24-well plates and transiently transfected using Lipofectamine 2000, following the manufacturer's recommended protocol (Invitrogen Corporation, Carlsbad, Calif.). Twenty-four hours post transfection, cells were trypsinized and re-plated into black-walled clear-bottom 96-well plates (Costar #3603) at 3×105 cells/well in 100 μl complete media. The following day, cells were loaded by adding 20 μl 6×CCF4-AM loading solution into each well (wells already contain 100 μl complete media and cells, final volume was 120 μl) and incubating for 90 minutes at room temperature. One milliliter of 6×CCF4-AM loading solution was prepared by adding 12 μl of Solution A (1 mM CCF4-AM in dry DMSO) to 60 μl of Solution B (100 mg/ml Pluronic-F127 in DMSO containing 0.1% Acetic Acid) followed by vortexing. Then this combined solution was added to 940 μl Solution C with vortexing, for a final volume of 1 ml (final CCF4-AM concentration was 12 μM in the 6× stock, 2 μM final on cells). After 90 minutes loading at room temperature, cells were observed under fluorescence microscopy equipped with β-lactamase filters (e.g., Omega Filters #XF106-2 excitation: 400DF15, dichroic 420DCLP, emission: 435ALP or Chroma Filters #41031 excitation: HQ405/20x, dichroic: 425DCXR, emission: HQ430LP) and photographed. Exact excitation of CCF substrates is 409 nm, green emission is 520 nm and blue emission is 447 nm.
Cells were photographed under fluorescence microscopy in the presence of the loading dye. After the photographs were taken, the loading solution was aspirated from the wells and the cells were washed one time with PBS. After the wash, 70 μl 1×PBS was added to all wells and the plate was read on a Molecular Devices Spectra Max Gemini XS plate reader at excitation: 405 nm, emission (blue): 460 nm, emission (green): 530 nm. Subsequent to the whole cell read on the plate reader, the PBS was aspirated and replaced with 70 μL Tropix lysis buffer (0.1 M KCl, 0.2% Triton X-100). The plate was allowed to sit for 5 minutes at room temperature, at which time the plate was again read on the plate reader at excitation: 405 nm, emission (blue): 460 nm, emission (green): 530 nm.
Results and Discussion
To create the expression vector pcDNA6.2/FRT/V5-2/GW-GeneBlazer, an LR reaction was performed with pENTR/GeneBlazer™×pcDNA6.2/FRT/V5-2/DEST. The reaction was transformed into TOP10 cells and plated on LB/Amp plates. 2.5×105 colonies were obtained/per reaction. 10 colonies were screened by restriction analyses and 100% were found to be correctly recombined confirming that the att sites in pENTR/GeneBlazer™ are fully functional.
For expression analyses, GripTite 293 cells were transiently transfected with pcDNA6.2/FRT/V5-2-GW/GeneBlazer, alongside previously tested pcDNA6.2/nGeneBlazer-GW/lacZ and pcDNA6.2/cGeneBlazer-GW/lacZ. Forty-eight hours post transfection, cells were loaded with CCF4-AM and photographed under fluorescence microscopy (
Conclusion
Sequence analyses confirmed the fidelity of pENTR/GeneBlazer™. The Entry clone is compatible with G
Introduction
The β-lactamase gene, coupled with the CCF2 substrate, is an excellent reporter and detection system for protein expression in mammalian cells (Whitney et al. (1998) Nat. Biotechnol. 16:1329-33; and Zlokarnik, et al. (1998) Science 279:84-88). Destination vectors have been developed for expressing either N- or C-terminal fusions of the β-lactamase ORF with a gene of interest in mammalian cells. These vectors are built in the pcDNA6.2 backbone (CMV expression, tk polyA, blasticidin resistance) and are called pcDNA6.2/nGeneBlazer-DEST and pcDNA6.2/cGeneBlazer-DEST, for N- and C-term β-lactamase fusions, respectively. To extend the cloning options, these vectors have been converted to topoisomerase charged vectors which will allow for quick directional cloning of PCR products.
Examples are provided of the construction of vectors in which: 1) the foreground to background colony count ratio from a Topo cloning reaction is 10 to 1 or better, 2) the Topo cloning efficiency is greater than 90% for presence and directionality of insert, 3) the cloned insert performs predictably in a BP C
Materials and Methods
Construction of pENTR Spec-ccdB D-Topo
The Spectinomycin and ccdB genes were amplified with the primers SC1 and SC2 using the vector pDEST6-R4R3-aadA (Invitrogen Corporation, Carlsbad, Calif.) as template. SC1 5′ CACCGACATTTTTGTTTAAACTT TGGTACCTGGATCCTTT-3′ (SEQ ID NO:129), SC2 5′ GACATTTTTGTTTAAACT TTGGTACCTGGATCCTTTAATTATTTGCCGACTACCTTGGT 3′ (SEQ ID NO:130). The PCR amplified fragment was Topo cloned into pENTR D-TOPO to generate pENTR Spec/ccdB. Clones were verified by restriction endonuclease digestion and DNA sequencing analysis.
Construction of pcDNA6.2/nGeneBlazer-GW/D.3 and pcDNA6.2/cGeneBlazer-GW/D.3
pENTR Spec/ccdB linearized with HpaI was reacted with either pcDNA6.2/nGeneBlazer-DEST linearized with EcoRI or pcDNA6.2/cGeneBlazer-DEST linearized with EcoRI in an LR reaction. A 2 μl aliquot of the LR reaction was transformed into DB3.1 cells and plated onto LB-Amp-Spec plates (Amp 100 μg/ml, Spec 100 μg/ml, Spectinomycin Sigma catalog number S-4014). The resulting clones, pcDNA6.2/nGeneBlazer-GW/D.3 and pcDNA6.2/cGeneBlazer-GW/D.3, were verified by restriction endonuclease digestion and DNA sequencing analysis.
BaeI Topo Adaptation Protocol
Twenty micrograms of either pcDNA6.2/nGeneBlazer-GW/D.3 or pcDNA6.2/cGeneBlazer-GW/D.3 were digested with 100 Units of BaeI (NEB, lot #2) in a final volume of 250 μl. Any other restriction enzyme known in the art may be als be used, for example, a Type II restriction enzyme such as a Type IIs restriction enzyme. The reaction was carried out in 1× NEBuffer 2 with 100 μg/ml of BSA and 20 μM S-adenosylmethionine at 37° C. for 6 hours. The BaeI digest was terminated with the addition of 250 μl of Phenol/Chloroform (Invitrogen, Cat. #15593-031) and mixed vigorously. The organic and aqueous phases were separated by centrifugation at 14,000×g at 4° C. for 5 minutes. The aqueous (top) layer was transferred to a new tube and 25 μl of 3M sodium acetate (pH 5.2) was added and mixed. This was followed by 625 μl of 100% ethanol and incubated in ice for 5 minutes. Precipitated DNA was harvested by centrifugation at 14,000×g for 5 minutes at 4° C. The DNA pellet was washed with 500 μl of 70% ethanol, harvested by centrifugation at 14,000×g for 5 minutes at 22° C. The pellet was allowed to dry and then resuspended in 100 μl of TE. The DNA concentration was determined by its optical density at 260 nm.
The sequences of the oligos used for Topo-charging are provided in
For the Topo-charging reaction, 5 μg of BaeI linearized DNA was mixed with 1.5 μg of Topo-D70 Annealing oligo and 5 μg of Vaccinia DNA Topoisomerase in 1× NEBuffer #1 at a final volume of 50 μl. The reaction was incubated at 37° C. for 15 minutes. Then terminated with the addition of 5 μl of 10× Stop Buffer. The Topo charged vector was purified by gel electrophoresis (see, Heyman, et al. Genome Research 9:383-392 (1999)).
NotI/AscI Adaptation Protocol
Eighty micrograms of either pcDNA6.2/nGeneBlazer-GW/D.3 or pcDNA6.2/cGeneBlazer-GW/D.3 was digested with 480 units of NotI (NEB, lot #49) in 400 μl of 1× NEBuffer #3 with 100 μg/ml of BSA (NEB) at 37° C. for 3 hours. This was followed by a phenol/chloroform extraction, DNA precipitation with sodium acetate and ethanol, and resuspension in 100 μl of water. The AscI digest was then performed with 480 units of AscI (NEB, lot#10) in 480 μl of 1× NEBuffer #4 at 37° C. for 3 hours. This was followed by a phenol/chloroform extraction, DNA precipitation with sodium acetate and ethanol, and resuspension in 50 μl of water. To this resuspended DNA the following oligonucleotides were added, Topo D-90 (30 μg), Topo D-74 (14 μg), Topo D-75 (30 μg) and Topo D-76 (9 μg).
Ligation of the oligonucleotides to the NotI/AscI digested vector was performed in 150 μl of 1× Invitrogen T4 DNA ligase buffer with 20 U of Invitrogen T4 DNA ligase. The ligation reaction was performed at 14° C. for 16 hours. This was followed by a phenol/chloroform extraction, DNA precipitation with sodium acetate and ethanol, and resuspension in 175 μl of TE as described above. Excess oligonucleotides were removed with 3 sodium acetate/isopropanol precipitations and the final DNA pellet was resuspended in 42 μl of TE. The concentration of the final DNA solution was determined by agarose gel electrophoresis, ethidium bromide staining and estimation with a predetermined DNA mass ladder.
For the Topo-charging reaction, 5 μg of adapted DNA was mixed with 1.5 μg of Topo-D70 annealing oligo and 5 μg of Vaccinia DNA Topoisomerase in 1× NEBuffer #1 at a final volume of 50 μl. The reaction was incubated at 37° C. for 15 minutes. The reaction was terminated with the addition of 5 μl of 10× Stop Buffer. The Topo charged vector was purified by the Topo-vector Gel Purification protocol.
Topo Adaptation Efficiency Assay
The standard 750 bp D-Topo PCR product was used to assess the cloning efficiency of the Topo-charged β-lactamase fusion vectors. Twenty nanograms of PCR product was reacted with 1 μl of the Topo-charged vector in a final reaction volume of 6 μl. Two microliters of the reaction was used to transform 50 μl TOP10 cells and the number of colonies resulting from this transformation reaction counted. As a control reaction a similar reaction was performed without the PCR product added.
TOPO Cloning of the CAT Gene
For TOPO cloning into Topoisomerase-charged pcDNA6.2/nGeneBlazer-GW/D.3, the CAT gene was amplified with the primers CATcacc and CATantiNS using pDEST6 as the PCR template. For TOPO cloning into Topoisomerase charged pcDNA6.2/cGeneBlazer-GW/D.3 the CAT gene was amplified with the primers CATcacc and CATantiS using pDEST6 as the PCR template. CATcacc 5′ CACCATGGAGAAAAAAATC ACTGG 3′, CATantiNS 5′ CTACGCCCCGCCCTGCCACTCAT 3′, CATantiS 5′ CGCCCCGCCCTGCCACTCAT 3′. Standard Topo cloning reactions were performed with the PCR amplified CAT ORFs.
BP Reactions with pcDNA6.2/nGeneBlazer-TopoCAT and pcDNA6.2/cGeneBlazer-TopoCAT
Both CAT expression vectors were digested with BglII prior to their use in a BP reaction. After a 3 hour incubation with BglII the digestion reaction was incubated at 80° C. for 90 minutes to inactivate the BglII enzyme. The BP reaction was performed with 150 ng of pDONR221, 50 ng of either pcDNA6.2/nGeneBlazer-TopoCAT or pcDNA6.2/cGeneBlazer-TopoCAT, 4 μl of BP C
Expression analysis of pcDNA6.2/nGeneBlazer-TopoCAT and pcDNA6.2/cGeneBlazer-TopoCAT by in vivo β-lactamase activity detection
A total of four miniprep cultures of independently isolated clones were used to inoculate 100 mL midipreps denoted pcDNA6.2/nGeneBlazed/dTOPO/CAT #32, pcDNA6.2/nGeneBlazer/dTOPO/CAT #36, pcDNA6.2/cGeneBlazer/dTOPO/CAT #38, and pcDNA6.2/cGeneBlazer/dTOPO/CAT #48. DNAs were isolated using the S.N.A.P. Midiprep kit (Invitrogen Corporation, Carlsbad, Calif.).
GripTite 293 cells were plated in 24-well plates and transiently transfected using Lipofectamine 2000, following the manufacturer's recommended protocol (Invitrogen Corporation, Carlsbad, Calif.). Forty-eight hours post transfection, cells were labeled with CCF4-AM to detect β-lactamase activity.
In vivo β-lactamase detection using CCF4-AM was performed as follows. Twenty-four hours post transfection, cells were trypsinized and re-plated into black-walled clear-bottom 96-well plates (Costar #3603) at 3×105 cells/well in 100 μl complete media. The following day, cells were treated by addition of 20 μl 6×CCF4-AM loading solution to each well (wells already contain 100 μl complete media and cells, final volume was 120 μl) and incubation for 90 minutes at room temperature. One milliliter of 6×CCF4-AM loading solution was prepared by adding 12 μl of Solution A (1 mM CCF4-AM in dry DMSO) to 60 μl of Solution B (100 mg/ml Pluronic-F127 in DMSO containing 0.1% Acetic Acid) followed by vortexing. This combined solution was added to 940 μl Solution C with vortexing, for a final volume of 1 ml (final CCF4-AM concentration was 12 μM in the 6× stock, 2 μM final on cells). After 90 minutes loading at room temperature, cells were observed under fluorescence microscopy equipped with β-lactamase filter (excitation: HQ405/20x, dichroic mirror: 425 DCXR, emission: HQ435LP; Omega Filters #XF106-2) and photographed. Exact excitation of CCF substrates is 409 nm, green emission is 520 nm and blue emission is 447 nm.
Cells were photographed under fluorescence microscopy in the presence of the loading dye. β-lactamase activity from the expressed fusion proteins was readily detectable as blue fluorescent cells. After the photographs were taken, the loading solution was aspirated from the wells and the cells washed once with PBS. After the wash, 100 μl 1×PBS was added to all wells and the plate was read on a Molecular Devices Spectra Max Gemini XS plate reader (405±10 nm, emission (blue): 460±20 nm, emission (green): 530±15 nm). Subsequent to the whole cell read on the plate reader, the PBS was aspirated and replaced with 70 μl Tropix lysis buffer. The plate was allowed to sit for 5 minutes at room temperature, at which time the plate was again read on the plate reader.
Expression analysis of pcDNA6.2/nGeneBlazer-TopoCAT and pcDNA6.2/cGeneBlazer-TopoCAT by immuno-detection of β-lactamase-CAT fusions
COS-7 cells were seeded in 24-well format at a density of 8×104 cells/well. COS-7 cells were plated with 500 μl of DMEM containing 10% FBS, 4 mM L-glutamine, and 0.1 mM non-essential amino acids. The following day the media was aspirated and fresh media was added prior to transfection.
The following are the vectors that were transfected in duplicate: pcDNA6.2/nGeneBlazed/dTOPO/CAT #32 pcDNA6.2/nGeneBlazer/dTOPO/CAT #36 pcDNA6.2/cGeneBlazer/dTOPO/CAT #38 pcDNA6.2/cGeneBlazer/dTOPO/CAT #48 pcDNA6/CAT (unfused CAT control) pcDNA/GW-53/CAT (N-terminally fused GFP-CAT control) pcDNA5/FRT/CAT/V5-His (C-terminally fused V5-His-CAT control)
Transfection cocktails were made with each of the vectors as follows:
In addition to the above listed plasmids 100 ng of pcDNA5/FRT/Luciferase was co-transfected with each of the above listed plasmids as an internal control for determining transfection efficiency. Lipofectamine 2000 was added to the OPTI-MEM and allowed to equilibrate for 5 minutes at room temperature. Each of the DNAs was added to a separate tube of OPTI-MEM. Duplicates were not set up as a master mix, but rather, individually. After the 5-minute incubation, 50 μl of the LF2K in OPTI-MEM was added to each tube containing DNA and allowed to complex for 20 minutes at room temperature. Upon completion of the incubation, 100 μl of lipid/DNA complex was added to each well. Twenty-four hours after transfection, the media was aspirated from the wells, and the cells from each well were lysed with 100 μl of 1×IGE PAL CA-630 lysis buffer (Sigma) with Complete Protease Inhibitor (Roche, 50× in H2O) and Pepstatin (Roche, 1000× in EtOH). Lysates were harvested into 1.5 ml eppendorf tubes and centrifuged for 2 minutes at maximum speed. Cleared lysates were transferred to new tubes. During assays, lysates were kept on ice and then stored at −80° C.
Protein Assay
In a 96 well U-bottom flexible polyvinyl chloride plate (Falcon Cat. No. 35-3911) cell lysates were diluted 1:10 in H2O (9 μL of H2O and 1 μL of lysate). In duplicate, 10 μl of BSA standard curve was added to the plate (1000 μg/ml serial diluted 1:2 down to 15.625 μg/ml). One hundred and ninety microliters Bradford reagent were added to the μl of diluted lysates and standard curve (1:5 dilution of BioRad Protein Assay Solution Cat. No. 500-0006, 1 ml Solution and 4 ml H2O). Using the plate reader and SoftMaxPro software, the endpoint wavelength was read at 595 and reduced numbers were displayed using the 4-parameter fit for the graph.
Western Blotting and Immuno-Detection Analysis
Samples run on the western blot gel included 15 μg of lysate, 4 μl of 4× NuPage Sample Buffer containing 0.4 μl volume of 2-Mercaptoethanol, and H2O to 20 μl. Samples were heated at 70° C. for 10 minutes (with vortexing and centrifugation throughout) prior to loading 20 μl on a 4-12% NuPage Bis-Tris gel. The following controls were also added to the gel: 5 μl of Magic Mark, and 10 μl of See Blue Plus 2. 1× NuPage MOPS SDS Sample Running Buffer was used. Five hundred microliters of NuPage Antioxidant was added to the sample running buffer in the “inner core”. The gel was run for approximately 50 minutes at 200 volts.
NuPage Transfer Buffer was prepared with 20% methanol. One milliliter of Antioxidant was added to 1 liter of 1× NuPage Transfer Buffer. PVDF membranes were wetted in methanol, rinsed with H2O, and then equilibrated in Transfer Buffer. Proteins from the gels were transferred to PVDF membrane for 90 minutes at 40 volts. Procedures from the NuPage Bis-Tris gel package insert were followed.
Following transfer, membranes were washed twice with 20 ml of H2O and blocked for 30 minutes with the blocking solution in the anti-rabbit Western Breeze Chemiluminescent Kit. Diluted anti-CAT antibody (Sigma) to 10 μg/ml in primary antibody diluent for PVDF membranes from the anti-rabbit Western Breeze Chemiluminescent Kit. All the procedures recommended in the Western Breeze Chemiluminescent Kit were followed.
Results and Discussion
Construction of pENTR Spec-ccdB D-Topo
The Spectinomycin-ccdB cassette within pENTR Spec-ccdB D-Topo allows for Topo adaptation of G
The Spec-ccdB cassette allows for Topo adaptation with the NotI/AscI sites to generate D-Topo, Blunt-Topo or TA Topo vectors however the BaeI sites are designed specifically to generate D-Topo vectors. The cassette is also movable to any Destination vector using a LR C
Construction of pcDNA6.2/nGeneBlazer-GW/D.3 and pcDNA6.2/cGeneBlazer-GW/D.3
pcDNA6.2/nGeneBlazer-GW/D.3 and pcDNA6.2/cGeneBlazer-GW/D.3 were constructed by moving the spec-ccdB cassette into either pcDNA6.2/nGeneBlazer-DEST or pcDNA6.2/cGeneBlazer-DEST using a LR C
The DTopo 750 bp PCR amplified fragment was used to assess the Topo cloning efficiency of the Topo-adapted vectors. Background colony numbers were generated from reactions containing no PCR product. The transformation competency of the TOP10 cells was determined to be 1010 cfu/ug.
Topo Adaptation Efficiency Assay
Plasmid DNA of 10 colonies from each of the Topo reactions described above were isolated to determine the presence and the orientation of the cloned 750 bp fragment. All clones isolated demonstrate that the 750 bp PCR amplified fragment was cloned and in the correct orientation except for one clone, which showed a clone bearing no insert. DNA sequence analysis confirmed that the junctions of the Topo cloned DNA ends were the predicted sequences.
Cloning efficiency of Topo vectors adapted with the Bad Topo adaptation protocol was assessed. The 750 bp fragment was Topo cloned into Topo charged pcDNA6.2/cGeneBlazer-GW/D.3 and plasmid DNA isolated from 10 of the colonies generated was digested with AvaI and showed the predicted digestion profile. The AvaI digest of plasmid DNA from positive clones will yield 3.9 kb and 2.7 kb DNA fragments. The 750 bp fragment was Topo cloned into Topo charged pcDNA6.2/nGeneBlazer-GW/D.3 and plasmid DNA isolated from 10 of the colonies generated was digested with AvaI. The AvaI digest of plasmid DNA from positive clones will yield 4.7 kb and 1.8 kb DNA fragments. All clones analyzed showed the predicted digestion profile.
Cloning efficiency of Topo vectors adapted with the NotI/AscI Topo adaptation protocol was assessed. The 750 bp fragment was Topo cloned into Topo charged pcDNA6.2/cGeneBlazer-GW/D.3 and plasmid DNA isolated from 10 of the colonies generated was digested with AvaI. The AvaI digest of plasmid DNA from positive clones will yield 3.9 kb and 2.7 kb DNA fragments. All clones analyzed showed the predicted digestion profile. The 750 bp fragment was Topo cloned into Topo charged pcDNA6.2/nGeneBlazer-GW/D.3 and plasmid DNA isolated from 10 of the colonies generated was digested with AvaI. The AvaI digest of plasmid DNA from positive clones will yield 4.7 kb and 1.8 kb DNA fragments. All but one of the clones showed the predicted digestion profile.
BP Reactions with pcDNA6.2/nGeneBlazer-TopoCAT and pcDNA6.2/cGeneBlazer-TopoCAT
The G
BP reaction were conducted with pDONR221 and pcDNA6.2/nGeneBlazer-TopoCAT or pcDNA6.2/cGeneBlazer-TopoCAT. Total colonies generated from BP reactions with CAT-β-lactamase fusion expression clones and pDONR221 were determined. The colony numbers are averages from 2 independent reactions. Plasmid DNA of 4 colonies from each of the BP reactions were digested with BsrGI. The BsrGI digestion of pENTR-CAT will yield 2.5 kb and 0.7 kb DNA fragments. All clones tested showed the correct digestion pattern.
Expression Analysis of pcDNA6.2/nGeneBlazer-Topo CAT and pcDNA6.2/cGeneBlazer-TopoCAT
The expression data of pcDNA6.2/nGeneBlazer-TopoCAT and pcDNA6.2/cGeneBlazer-TopoCAT is shown in
GripTite 293 cell lines demonstrating β-lactamase expression were prepared and digital images were prepared and are shown in
Expression of CAT in GeneBlazer dTOPO plasmids was assessed by Western blot and the results are shown in
In conclusion, the Topo-charged pcDNA6.2/nGeneBlazer-GW/D.3 and pcDNA6.2/cGeneBlazer-GW/D.3 have met the key performance criteria. The Topo cloning efficiency with respect to the foreground and background colony numbers was greater than 90%, the cloning of an insert with directionality was shown to be 95% and the resulting clones from the Topo reaction were active in a BP reaction and produced β-lactamase fusion proteins with β-lactamase activities comparable to β-lactamase fusion proteins cloned by G
Summary
Four new pET based vectors were constructed that carry the His6 purification and L
Introduction
Expression of recombinant proteins plays an important role in analyzing gene regulation, structure and function. As more genome sequence data becomes available for an ever-growing list of organisms, a major challenge will be to rapidly clone and express multiple genes across several expression platforms. Additionally, sufficient quantities of proteins will be required for meaningful analysis. Finally, a rapid detection method for) determining recombinant protein expression would be highly desirable. By combining the high-yield bacterial pET expression system, the state of the art G
The L
The sequence Cys-Cys-Pro-Gly-Cys-Cys was shown to give the complex much more stability and increased affinity (Adams, S. R., Campbell, R. E., Groww, L. A., Martin, B. R., Walkup, G. K., Tao, Y., Llopis, J., Tsein, R. Y. J. (2002) Am. Chem. Soc., 124: 6063-6076). The sequence Ala-Gly-Gly was added to the N-terminus and Gly-Gly-Gly to the C-terminus to avoid any interference with the surrounding motifs and to better present the epitope when generating antibodies against the tag. The DNA sequence encoding the L
The optimized L
Four new pET based Destination and d-TOPO™ vectors, referred to as pET160-DEST, pET161-DEST, pET160/D-TOPO™, and pET161/D-TOPO™, were constructed that contained the L
Materials and Methods
Bacterial Strains and Growth Conditions.
The Escherichia coli strains TOP10, DH5alpha, and DB3.1 were used for cloning while BL21 Star [F− ompT hsdSB (rB−mB−) gal dcm rne131 (DE3)] was used for gene expression. Standard media and growth conditions were used for E. coli (growth at 37° C. in LB). Ampicillin was used at 100 μg/ml in plates and media. Chloramphenicol was used at 10 μg/ml in plates and media. Kanamycin was used at 25 μg/ml in plates and media.
Construction of pET160/L
The vector was constructed by mutagenesis of pET-DEST151 (
The two primers were mixed together with the pET-DEST151 template and the fragment was amplified by PCR. The PCR product was cloned into pCR2.1 (Invitrogen Corp., Carlsbad, Calif., cat no. K2000-01). After sequence verification, the pCR2.1/F
Construction of pET161/L
The vector was constructed by cassette mutagenesis of pET-DEST42 (Invitrogen Corp., Carlsbad, Calif., cat no. 12276-010). Two primers were synthesized that when annealed created an oligo containing the L
The reaction was placed in a thermocycler and run through 5 cycles of 96° C. for two minutes, 55° C. for 1 minute, and 72° C. for 1 minute. The product was cloned into pCR2.1. A positive clone was sequence verified and digested with BstBI and AgeI. The purified fragment was ligated into BstBI and AgeI digested pET-DEST42 to create the pET-DEST42/F
The pET-DEST42/F
The translational enhancer was added by digesting the pET-DEST42/151/F
TOPO™ Adaptation of pET160/L
The vectors were prepared with the Qiagen Mega Prep kit from 500 ml LB with chloramphenicol. The pET160/L
TOPO™ Charging of pET160/D-TOPO™ and pET161/D-TOPO™.
The pET160 and 161 D-TOPO vectors were TOPO adapted essentially as follows:
Final Vector Formulation: 10 ng/μl plasmid DNA in:
50% glycerol
100 μg/ml BSA
30 μM bromophenol blue
Procedure:
NotI/AscI Digest
100 μg of supercoiled DNA was digested with NotI using 6 Units/μg of DNA at a final vector concentration of 0.25 μg/ml. The mixture was then incubated in a 37° C. incubator for 3 hours with occasional mixing/spinning. The mixture was then extracted with ½ volume phenol/chloroform followed by precipitation with 1/10 volume 3M Sodium Acetate and 2× volume room temperature Ethanol. The pellet was then washed with 80% Ethanol. The pellet was then resuspended in nuclease-free water to a DNA concentration of 1 μg/μl and 1 μg was run on a 0.8% agarose gel to verify 100% digestion. Once complete digestion with NotI was confirmed, the linear DNA was digested with AscI as described above for NotI. Following AscI digestion and purification, the pellet was resuspended in nuclease-free water to a DNA concentration of 1 μg/μl.
Adaptor Ligation/Purification
Unless other wise stated, the following methods were performed at room temperature. With a final volume of 200 quantities of the following components were calculated and added in the order listed below:
The tube was inverted, spun briefly, and incubated at 12° C. overnight. The solution was then extracted with 1 volume of phenol chloroform and precipitated with 1/10 volume of 3M Sodium acetate and 2× volume Ethanol. The pellet was washed with 80% Ethanol and then resuspended in TE Buffer to a DNA concentration of 1 μg/μl. 1/10 volume 3M Sodium acetate and 0.7 volume Isopropanol was added at room temperature and the solution was mixed. The solution was then spun at high speed for 1 minute and the supernatant removed. The pellet was then resuspended in TE Buffer and twice reprecipitated as described above for a total of 2 isopropanol precipitations to ensure that excess adaptors were removed. The final pellet was then washed with 80% Ethanol. The pellet was then resuspended in TE Buffer to a DNA concentration of 1 μg/μl.
Topoisomerase Reaction and Gel Purification.
Unless other wise stated, the following methods were performed at room temperature. A 0.9% agarose gel containing a 1 mm thick comb was prepared. The comb was removed and a fresh solution of 1×TAE buffer was added to the reservoirs up to the top edges of the gel without allowing the buffer to touch the top of the gel or enter the wells.
TopoD-70 was added to the solution of linear DNA to a concentration of 0.325 μg/μg of linear DNA.
2.375 μl of 10×NEB Restriction Buffer #1 was then added per μg of linear DNA and the solution was mixed well.
The DNA concentration was adjusted to 0.042 μg/μl with Medical Irrigation water. Vaccinia Topoisomerase I enzyme was then added to a concentration of 1 μg/μg of linear DNA. The mixture was then incubated at 37° C. for 15 minutes with mixing once in the middle of the incubation. After 15 minutes, the reaction was stopped by adding 2.5 μl of 10× Stop Buffer per μg of linear DNA and brief mixing. The mixture was then spun and then the supernatant was collected.
The total volume of reaction was run on an agarose gel at 70 volts for 15 minutes until the bromophenol blue dye ran down about ½ inch into the gel. While the gel was running, a new sterile container was chilled on ice. The voltage was reversed and the gel was run backwards for 90 seconds, and then the power supply was turned off. The solution was removed from the wells and transferred to the pre-chilled container. 2× Wash Buffer (blue) was then added to the well and allowed to sit in the well for 1 minute.
The wells were then vigorously rinsed with the 2× Wash Buffer (blue) to resuspend any DNA trapped at the edges of the well and then transferred to the pre-chilled container. An equal volume of Glycerol Mix was added to the pre-chilled container and the solution was mixed gently by inversion to avoid the formation of bubbles. The solution was then spun and stored at −20° C. for 2 weeks or less, or at −80° C. for long term storage.
The prepared vectors were tested essentially as follows. Briefly the 750 bp BSD PCR Control was amplified using Pfu DNA Polymerase (Stratagene, La Jolla, Calif. 92037, cat. no. 600153). One microliter of the PCR reaction was used in a 6 μl directional TOPO™ reaction. Two microliters of the TOPO™ reaction were transformed into Top10 chemically competent cells. After a one hour incubation in 300 μl SOC shaking at 37° C., 100 μl was plated on LB/AMP plates. Colonies were counted to determine cloning efficiency and minipreps were checked by restriction analysis to determine percent of directional clones.
LR Recombination of Entry Clones with pET160-DEST and pET161-DEST.
Fusion protein expression constructs were generated using the pENTR kinase vectors. Kinase entry clones were obtained from the Ultimate ORF Collection. Constructs containing a stop codon and were used in the LR reaction with pET 160-DEST. A pENTR-CAT construct, which is similar to the vectors of cat. nos. 12562-013 and 12562-039 sold by Invitrogen Corp, Carlsbad, Calif., containing a stop codon was also used to generate the G
D-TOPO™ Reaction with pET160/D-TOPO™ and pET161/D-TOPO™
Primers were designed to clone the CAT gene into the pET/D-TOPO™ vectors.
The forward primers contained C/ACC/ATG sequence enabling directional cloning and an initiation codon. The dTOPO™CAT-STOP reverse primers had a TAG stop for cloning into the N-terminal vector. The dTOPO™CAT-NS reverse primer did not contain a stop codon and allowed for translation of the C-terminal fusion. PCR products were amplified using the appropriate primers and 2.5 U Pfu Polymerase (Stratagene) in the 1×Pfu Buffer with 50 μM dNTP's for 25 cycles.
The PCR product was directionally TOPO™ cloned into the prepared pET-DEST160 D-TOPO™ vectors which were used to transform into DH5alpha cells and plated on plates containing LB agar plates containing ampicillin. Colonies were screened by DNA miniprep and restriction digests. A positive clone from each was transformed into BL21 Star cells for expression testing and are the positive control vectors for the kits.
BP Recombination of Expression Clones with pDONR201
The pET160/CAT vector and pET161/Kinase C8 were used in BP reactions with pDONR201 (Invitrogen Corp, Carlsbad, Calif., cat. nos. 11798-014 and 11821-014) to regenerate entry clones. One hundred nanograms of each vector was linearized with XbaI for 1 hour at 37° C. The plasmid was gel purified and used in a 20 μl BP reaction with 300 ng pDONR201 (pET160 construct) and pDONR221 (pET161 construct) (Invitrogen Corp, Carlsbad, Calif., cat. nos. 12535-019 and 12536-017), 4 μl BP CLONASE™ Enzyme Mix (Invitrogen Corp, Carlsbad, Calif., cat. no. 11789-021), 1× Reaction Buffer and TE. After incubation at 25° C. for 1 hour, 2 μl of Proteinase K solution was added and incubated for 10 minutes at 37° C. One microliter of the reaction was used to transform DH5alpha competent cells and they were plated on LB agar plates containing 50 μg/ml kanamycin. Minipreps were performed on the resulting colonies and restriction analysis confirmed the fidelity of the recombination reactions.
Expression of Fusion Proteins in pET160-DEST and pET161-DEST.
The pET-DEST vectors carrying expression proteins were introduced into BL21 Star cells. Four ml LB ampicillin were innoculated with 20 μl of an overnight culture or with five colonies from an overnight plate. Cells were grown to A600=0.4 and induced in 1 mM IPTG for three hours at 37° C. Cells (1 ml) were harvested by centrifugation, and resuspended in 0.1 ml of 1× Running Buffer. Cell lysates were prepared by equilibrating 10 μl of cell suspension to 50 mM F
Detection of Epitope Tags by Immunoblotting.
The mouse-anti-H isG or mouse-anti-His C antibody (Invitrogen Corp., cat. nos. R94025 and R93025) was used to detect epitope tags by immunoblotting (1:5000 dilution). After SDS/PAGE separation, proteins were blotted to nitrocellulose, and detected using the W
Purification of Recombinant Proteins by ProBond Metal Affinity Chromatography.
BL21 Star cells were transformed with pET160-GW/Kinase H45 (BC007462) or with pET161-GW/CAT. From a single colony, cells were grown overnight at 37° C., and inoculated 1/100 into 250 ml LB ampicillin. Cells were induced with 1 mM IPTG at A600=0.4. After a 3 hour induction at 37° C., cells were pelleted by centrifugation and lysed as described in the ProBond manual (Invitrogen Corp, Carlsbad, Calif., cat. no. K850-01) for denatured purification conditions at a 5× scale. The lysate (40 ml) was loaded onto a prepared ProBond (20 ml) column, and the column was gently agitated for 30 minutes to allow for binding. The resin was allowed to settle and the supernatant was aspirated off. The column was washed with Denaturing Binding Buffer by gentle mixing for 2 minutes. The resin was allowed to settle, the supernatant aspirated off, and the procedure repeated 1 more time. The column was washed twice with Denaturing Wash Buffer pH 6.0 of the ProBond kit and twice with Denaturing Wash Buffer pH 5.3. Protein was eluted by adding 10 ml Denaturing Elution Buffer of the ProBond kit. Two ml fractions were collected and monitored by S
Cleavage of MBP Produced by pET160-DEST by TEV Protease.
BL21 Star cells were transformed with pET160-GW/MBP. From a single colony, cells were grown overnight in LB ampicillin at 37° C., and inoculated 1/100 in 50 ml LB ampicillin. Cells were induced with 1 mM IPTG at A600=0.4. After a 3 hour induction. Cells were pelleted by centrifugation and were lysed as described in the ProBond manual for native purification conditions. The lysate (8 ml) was loaded onto a prepared native ProBond (4 ml) column, and the column was gently agitated for 20 minutes to allow for binding. The resin was allowed to settle and the supernatant was aspirated off. The column was washed with 8 ml of Native Wash Buffer by gentle mixing for 2 minutes. The resin was allowed to settle, the supernatant aspirated off and the procedure repeated 3 more times. The column was clamped in a vertical position and the cap snapped off the lower end. Protein was eluted by adding 8 ml Native Elution Buffer. One ml fractions were collected and monitored. The native substrate was used for digestion with TEV protease (Invitrogen Corp, Carlsbad, Calif., cat. no. 10127-017).
Partially purified MBP was digested with TEV protease. Approximately 250 ng of protein isolated under native conditions was digested with 5 and 10 Units of TEV in 1×TEV Buffer for 3 hours at 37° C. Digested substrates were analyzed by SDS-PAGE (Novex, Tris-Glycine 4-20%).
In-Gel Detection of Protein in Lysates and Purified Proteins.
Protein lysates and purified protein samples were heated to 95-100° C. for 3 minutes in 1× Lammeli Sample Buffer (Lammeli, V. K. 1970. Theor. Appl. Genet. 85:882-888) supplemented with 25 μM F
G
A 96-well plate containing 92 Ultimate ORF Kinase entry clones was used to generate expression clones and proteins in a high-throughput format. The remaining 4 wells were controls. A 96 LR cross of pENTR Kinase clones into pET160-DEST was directly transformed into BL21 Star cells and 25 μl of the transformation was used to inoculate 750 μl of LB ampicillin in a deep well 96-well plate. Overnight seed cultures were diluted 1:40 in fresh LB ampicillin (1.5 ml) and grown at 37° C. to induction at A600=0.336 with 1 mM IPTG for 3 hours. Whole cell lysates were analyzed by SDS/PAGE as described above.
Results and Discussion
L×R Cloning and Expression Testing.
To demonstrate high-level expression from pET160-DEST, the vector was used in eight L×R reactions with pENTR-Kinases A1-H1 from the 96-well kinase plate. Positive clones were identified and transformed into BL21 Star cells for expression testing. The expression from lysates was seen in the S
To test expression from pET161-DEST (the C-terminal L
When expressing non-E. coli genes, the kinases C8 and D2 both expressed significantly better from pET161-DEST and pET161-DEST (ATG) compared to the parental plasmid (data not shown). In fact, the kinases could not be detected by F
The dTOPO™ (directional TOPO) Reaction and Expression Clone Induction
Both the pET-DEST/L
The CAT PCR product was directionally TOPO™ cloned into pET160/D-TOPO™. A positive clone was expressed in BL21 Star and compared to the pET160-GW/CAT construct. The cell lysate was detected by in-gel fluorescence, S
The BP Cloning Reaction
The functionality of the attB1 and attB2 sites of the pET160-GW/lacZ vector and pET161-GW/Kinase C8 were tested in BP reactions with pDONR201 or pDONR221 to regenerate entry clones. The BP reaction pET160-GW/lacZ into pDONR201 gave 171 cfu for the entire transformation in DH5alpha chemically competent cells. Five of the six colonies screened by restriction digest were positive for the correct recombination. The (−) control gave 0 cfu for the entire transformation. The BP reaction of pET161-GW/Kinase C8 into pDONR221 resulted in approximately 1000 colonies and gave 6/9 positive for the correct recombination. The (−) control gave 42 cfu for the entire transformation. These results indicate that the attB sites of both vectors are functioning properly and can easily generate the desired entry clones.
Functionality of His Tags in pET160 and pET161.
Both the H isG and C-terminal His antibodies recognize the His epitopes encoded by their respective vectors (data not shown). To verify that the His6 tags functioned properly as purification epitopes, the pET161-GW/CAT and the pET160-GW/Kinase H5 (BC007462) construct were expressed in BL21 Star cells. The lysates were purified by Probond column using denaturing conditions and fractions from the lysate, washes and elution were analyzed (
Functional Testing of TEV Protease Site in pET160.
To verify the recognition and proteolysis of the TEV cleavage site in the pET160 vector, the gene for Maltose Binding Protein (MBP) was crossed into pET160-DEST, expressed from BL21 Star and purified using ProBond nickel-chelating resin under native conditions. Approximately 250 ng of the partially purified protein was used in the reaction with TEV protease using standard conditions. In brief, MBP expression product was digested with either 5 or 10 Units of TEV protease for 3 hour digestion at 37° C. The digestion products we then analyzed by SDS-PAGE and compared against separate lanes which contained S
High Throughput Cloning, Expression, and in-Gel Detection of the Control 96-Well Kinase Plate.
To demonstrate the utility of pET160-DEST in a high-throughput format, the vector was crossed with pENTR Human Kinase clones, which were stored in the individual wells of a 96-well plate, and then transformed directly into BL21 STAR cells for overnight growth. Wells G2, A5, F5, B6, G7, and F11 had little or no growth in the overnight cultures. After dilution into fresh media and growth at 37° C., the cultures were induced for 3 hours and lysates prepared from each well. The samples were reacted with F
Conclusions
We have validated the utility of G
Protein expression monitoring was greatly facilitated by in-gel detection of proteins containing the L
In a protein BLAST database homology search, it was observed that the L
The pET160/L
Introduction
L
Protocol for in vivo labeling of transfected mammalian cells is provided below.
Materials And Methods
Materials:
Preparation of 20 mM Disperse Blue Stock Solution:
Weigh 593 mg of Disperse Blue 3 powder (50 g, MW=296.32). Add 100 mL of dry DMSO to the Disperse Blue powder and mixed thoroughly by vortexing to dissolve. Pass solution through a 0.2 um filter.
To qualify the 20 mM Disperse Blue 3 stock solution, prepare 25 mL of 50% ethanol in water. Place 10 mL of the 50% ethanol solution in each of two 15 mL polypropylene tubes. Add 16.875 μl of the filtered 20 mM Disperse Blue 3 test sample prepared above to the first tube. This solution should be 3.375×10−5 M. Add 16.875 μl of 20 mM Disperse Blue 3 stock solution to the second tube. This solution is 3.375×10−5 M. Vortex each tube thoroughly. Using a spectrophotometer with a 1 cm path length, measure the absorbance of the diluted Disperse Blue 3 solutions at 638 nm, 593 nm and 256 nm wavelengths. Use quartz cuvettes and blank the instrument at each of these wavelengths with the extra 50% ethanol prepared above. Table 6 below provides the extinction coefficients for each wavelength and the range of absorbance values that should be obtained at each wavelength. These values will be used to evaluate the dye content of the test sample of Disperse Blue 3.
If the absorbance values of the Disperse Blue 3 do not fall within the range of expected absorbance values, repeat the qualification procedure described above.
If the absorbance values obtained for the test sample of Disperse Blue 3 fall below the expected absorbance range, this indicates that the dye content of the 20 mM stock solution is not concentrated enough and needs to be adjusted (see formula below).
(Absorbance)/(extinction coefficient)=concentration (in Molar units)
Eg. If absorbance 638 nm reads 0.180, then [0.180]/[6,600]=2.727×10−5 M
Adjust accordingly and re-QC.
Conversely, if the absorbance values measured for the sample of Disperse Blue falls above the expected absorbance range, this indicates that the dye content of the 20 mM stock solution is too high and it needs to be diluted (see formula above).
Eg. If absorbance 638 nm reads 0.260, then [0.260]/[6,600]=3.939×10−5 M
In vivo Labeling Protocol:
Day 1: Plate Cells For Transfection.
Plate GripTite™ 293 cells into 6-well plates at 6×105 cells per well. Four wells are used for every L
Day 2: Transfection.
Transfect cells with 4 μg of vector which expresses a protein or peptide with a L
Day 3:
Change media on transfected cells to regular growth media.
Day 4: L
Prepare 2 mL of 2.5 μM L
Evaluate L
Note: L
The following example is intended to illustrate exemplary methods for carrying out the present invention. Variations on the methods set forth herein will be readliy appreciated by those skilled in the art. The information set forth in this or any other example should not be construed as limiting the scope of the invention described herein. All catalog numbers mentioned in this example refer to specific products and reagents available from Invitrogen Corporation, Carlsbad, Calif., 92008. The exemplary methods described herein can be carried out using the products and reagents designated by the catalog numbers, or with equivalent products and reagents available from other sources.
E. coli
E. coli
The Genotype of Mach1™-T1R Cells is as follows: F− φ80(lacZ)ΔM15 ΔlacX74 hsdR(rK−mK+) ΔrecA1398 endA1 tonA Use this strain for cloning. Note that this strain cannot be used for single-strand rescue of DNA.
Additional products that may be used with the GeneBLAzer™ TOPO® Fusion Kits are available from Invitrogen and are listed in Table 14.
E. coli
Introduction
The GeneBLAzer™ TOPO® Fusion Kits provide a highly efficient, 5-minute cloning strategy (“TOPO® Cloning”) to directionally clone a blunt-end PCR product into a reporter vector for expression in mammalian cells. The pcDNA6.2/GeneBLAzer-GW/D-TOPO® vector supplied with each kit facilitates in vivo or in vitro detection of β-lactamase reporter activity in mammalian cells using the GeneBLAzer™ Technology. Use of the GeneBLAzer™ Technology provides a highly sensitive and accurate method to quantitate gene expression in mammalian cells.
The pcDNA6.2/GeneBLAzer-GW/D-TOPO® vectors also allow easy transfer of your gene of interest into multiple vector systems using Gateway® Technology.
Features of the pcDNA6.2/GeneBLAzer-GW/D-TOPO® Vectors
The pcDNA6.2/cGeneBLAzer-GW/D-TOPO® and pcDNA6.2/nGeneBLAzer-GW/D-TOPO® vectors contain the following elements:
Human cytomegalovirus immediate-early (CMV) promoter/enhancer for high-level expression in a wide range of mammalian cells;
β-lactamase bla(M) reporter gene for C-terminal (pcDNA6.2/cGeneBLAzer-GW/D-TOPO®) or N-terminal (pcDNA6.2/nGeneBLAzer-GW/D-TOPO®) fusion to the gene of interest;
attB1 and attB2 sites for site-specific recombination of the expression clone with a Gateway® donor vector to generate an entry clone;
Directional TOPO® Cloning site for rapid and efficient directional cloning of blunt-end PCR products;
The V5 epitope tag for detection using Anti-V5 antibodies (pcDNA6.2/nGeneBLAzer-GW/D-TOPO® only);
The Herpes Simplex Virus thymidine kinase polyadenylation signal for proper termination and processing of the recombinant transcript;
f1 intergenic region for production of single-strand DNA in F plasmid-containing E. coli;
SV40 early promoter and origin for expression of the Blasticidin resistance gene and stable propagation of the plasmid in mammalian hosts expressing the SV40 large T antigen;
Blasticidin resistance gene for selection of stable cell lines;
The pUC origin for high copy replication and maintenance of the plasmid in E. coli;
The ampicillin resistance gene for selection in E. coli.
For a map of pcDNA6.2/cGeneBLAzer-GW/D-TOPO® or pcDNA6.2/nGeneBLAzer-GW/D-TOPO®, see
The Gateway® Technology
The Gateway® Technology is a universal cloning method that takes advantage of the site-specific recombination properties of bacteriophage lambda (Landy, A. (1989). Dynamic, Structural, and Regulatory Aspects of Lambda Site-specific Recombination. Annu. Rev. Biochem. 58, 913-949) to provide a rapid and highly efficient way to move your gene of interest into multiple vector systems. To express your gene of interest in mammalian cells, simply TOPO® Clone your blunt-end PCR product into a GeneBLAzer™ Directional TOPO® vector and transfect your expression clone into the mammalian cell line of choice.
To express your gene of interest in any other expression system:
1. Generate an entry clone by performing a BP recombination reaction between your expression clone and a Gateway® donor vector.
2. Perform an LR recombination reaction between the entry clone and a variety of Gateway® destination vectors to generate an expression construct to express your protein of interest in virtually any expression system.
Advantages of the GeneBLAzer™ Technology
Using the GeneBLAzer™ Technology and the GeneBLAzer™ Detection System as a reporter of gene expression in mammalian cells provides the following advantages:
Suitable for use as a sensitive reporter of gene expression in living mammalian cells using fluorescence microscopy.
Provides a ratiometric readout to minimize differences due to variability in cell number, substrate concentration, fluorescence intensity, and emission sensitivity.
Compatible with a wide variety of in vivo and in vitro applications including microplate-based transcriptional assays and flow cytometry.
Provides a flexible and simple assay development platform for gene expression in mammalian cells.
Using a non-toxic substrate allows continued cell culturing after quantitative analysis.
One Shot® Mach1™-T1R E. coli
The Mach1™-T1R E. coli strain is modified from the wild-type W strain (ATCC #9637, S. A. Waksman) and has a faster doubling time compared to other standard cloning strains. With Mach1™-T1R cells, you can visualize colonies 8 hours after plating on ampicillin selective plates. You can also prepare plasmid DNA 4 hours after inoculating a single, overnight-grown colony in the selective media of choice. Note that this feature is not limited to ampicillin selection.
Additional features of the Mach1™-T1R E. coli strain include:
lacZΔM15 for blue/white color screening of recombinants;
hsdR mutation for efficient transformation of unmethylated DNA from PCR applications;
ΔrecA1398 mutation for reduced occurrence of homologous recombination in cloned DNA;
endA1 mutation for increased plasmid yield and quality;
tonA mutation to confer resistance to T1 and T5 phage.
Tag-On-Demand™ System
The pcDNA6.2/GeneBLAzer-GW/D-TOPO® vectors are compatible with the Tag-On-Demand™ System which allows expression of both native and C-terminally-tagged recombinant protein from the same expression construct.
The System is based on stop suppression technology originally developed by RajBhandary and colleagues (Capone, J. P., Sharp, P. A., and RajBhandary, U. L. (1985). Amber, Ochre and Opal Suppressor tRNA Genes Derived from a Human Serine tRNA Gene. EMBO J. 4, 213-221) and consists of a recombinant adenovirus expressing a tRNAser suppressor. When an expression vector encoding a gene of interest with the TAG (amber stop) codon is transfected into mammalian cells and the tRNAser suppressor supernatant is present, the stop codon will be translated as serine, allowing translation to continue and resulting in production of a C-terminally-tagged fusion protein.
How Directional TOPO® Cloning Works
How Topoisomerase I Works
Topoisomerase I from Vaccinia virus binds to duplex DNA at specific sites (CCCTT) and cleaves the phosphodiester backbone in one strand (Shuman, S. (1991). Recombination Mediated by Vaccinia Virus DNA Topoisomerase I in Escherichia coli is Sequence Specific. Proc. Natl. Acad. Sci. USA 88, 10104-10108). The energy from the broken phosphodiester backbone is conserved by formation of a covalent bond between the 3′ phosphate of the cleaved strand and a tyrosyl residue (Tyr-274) of topoisomerase I. The phospho-tyrosyl bond between the DNA and enzyme can subsequently be attacked by the 5′ hydroxyl of the original cleaved strand, reversing the reaction and releasing topoisomerase (Shuman, S. (1994). Novel Approach to Molecular Cloning and Polynucleotide Synthesis Using Vaccinia DNA Topoisomerase. J. Biol. Chem. 269, 32678-32684). TOPO® Cloning exploits this reaction to efficiently clone PCR products.
Directional TOPO® Cloning
Directional joining of double-strand DNA using TOPO®-charged oligonucleotides occurs by adding a 3′ single-stranded end (overhang) to the incoming DNA (Cheng, C., and Shuman, S. (2000). Recombinogenic Flap Ligation Pathway for Intrinsic Repair of Topoisomerase IB-Induced Double-Strand Breaks. Mol. Cell. Biol. 20, 8059-8068). This single-stranded overhang is identical to the 5′ end of the TOPO®-charged DNA fragment. At Invitrogen, this idea has been modified by adding a 4 nucleotide overhang sequence to the TOPO®-charged DNA and adapting it to a ‘whole vector’ format.
In this system, PCR products are directionally cloned by adding four bases to the forward primer (CACC). The overhang in the cloning vector (GTGG) invades the 5′ end of the PCR product, anneals to the added bases, and stabilizes the PCR product in the correct orientation. Inserts can be cloned in the correct orientation with efficiencies equal to or greater than 90%. See
The GeneBLAzer™ Technology
Components of the GeneBLAzer™ System
The GeneBLAzer™ System facilitates fluorescence detection of β-lactamase reporter activity in mammalian cells, and consists of two major components:
The β-lactamase reporter gene, bla(M), a truncated form of the E. coli bla gene. When fused to a gene of interest, the bla(M) gene can be used as a reporter of gene expression in mammalian cells. For more information about the bla(M) gene, see below.
A fluorescence resonance energy transfer (FRET)-enabled substrate, CCF2 to facilitate fluorescence detection of β-lactamase activity. In the absence or presence of β-lactamase reporter activity, cells loaded with the CCF2 substrate fluoresce green or blue, respectively. Comparing the ratio of blue to green fluorescence in a population of live cells or in a cell extract of your sample to a negative control provides a means to quantitate gene expression. For more information about the CCF2 substrate and how FRET works, refer to the GeneBLAzer™ Detection Kits manual.
β-Lactamase (bla) Gene
β-lactamase is the product encoded by the ampicillin resistance gene (bla) and is the bacterial enzyme that hydrolyzes penicillins and cephalosporins. The bla gene is present in many cloning vectors and allows ampicillin selection in E. coli. β-lactamase enzyme activity is not found in mammalian cells.
bla(M) Gene
The GeneBLAzer™ Technology uses a modified bla gene as a reporter in mammalian cells. This bla gene is derived from the E. coli TEM-1 gene present in many cloning vectors (Zlokarnik, G., Negulescu, P. A., Knapp, T. E., Mere, L., Burres, N., Feng, L., Whitney, M., Roemer, K., and Tsien, R. Y. (1998). Quantitation of Transcription and Clonal Selection of Single Living Cells with b-Lactamase as Reporter. Science 279, 84-88), and has been modified in the following ways:
72 nucleotides encoding the first 24 amino acids of β-lactamase were deleted from the N-terminal region of the gene. These 24 amino acids comprise the bacterial periplasmic signal sequence, and deleting this region allows cytoplasmic expression of β-lactamase in mammalian cells.
The amino acid at position 24 was mutated from His to Asp to create an optimal Kozak sequence for optimal translation initiation.
This modified reporter gene is named bla(M).
Note: The TEM-1 gene also contains 2 mutations (at nucleotide positions 452 and 753) that distinguish it from the bla gene in pBR322 (Sutcliffe, J. G. (1978). Nucleotide Sequence of the Ampicillin Resistance Gene of Escherichia coli Plasmid pBR322. Proc. Nat. Acad. Sci. USA 75, 3737-3741).
Experimental Outline
The table below describes the general steps needed to clone and express your gene of interest.
General Requirements for Designing PCR Primers
Designing Your PCR Primers
The design of the PCR primers to amplify your gene of interest is critical for expression. Consider the following when designing your PCR primers.
Sequences required to facilitate directional cloning;
Sequences required for proper translation initiation of your PCR product;
Sequences required to fuse your PCR product in frame with the β-lactamase reporter gene.
General Requirements for the Forward Primer
To enable directional cloning, the forward PCR primer must contain the sequence, CACC, at the 5′ end of the primer. The 4 nucleotides, CACC, base pair with the overhang sequence, GTGG, in each pcDNA6.2/GeneBLAzer-GW/D-TOPO® vector.
Example of Forward Primer Design
Below is the DNA sequence of the N-terminus of a theoretical protein and the proposed sequence for your forward PCR primer. The ATG initiation codon is underlined.
If you design the forward PCR primer as noted above, then the ATG initiation codon falls within the context of a Kozak sequence (see boxed sequence), allowing proper translation initiation of the PCR product in mammalian cells.
The first three base pairs of the PCR product following the 5′ CACC overhang will constitute a functional codon.
General Requirements for the Reverse Primer
In general, design the reverse PCR primer to allow you to clone your PCR product in frame with any C-terminal fusions, if desired. To ensure that your PCR product clones directionally with high efficiency, the reverse PCR primer MUST NOT be complementary to the overhang sequence GTGG at the 5′ end. A one base pair mismatch can reduce the directional cloning efficiency from 90% to 75%, and may increase the chances of your ORF cloning in the opposite orientation. We have not observed evidence of PCR products cloning in the opposite orientation from a two base pair mismatch, but this has not been tested thoroughly.
Example #1 of Reverse Primer Design
Below is the sequence of the C-terminus of a theoretical protein. You want to fuse the protein in frame with a C-terminal tag. The stop codon is underlined.
One possibility is to design the reverse PCR primer to start with the codon just up-stream of the stop codon, but the last two codons contain GTGG (underlined below), which is identical to the 4 bp overhang sequence. As a result, the reverse primer will be complementary to the 4 bp overhang sequence, increasing the probability that the PCR product will clone in the opposite orientation. You want to avoid this situation.
Another possibility is to design the reverse primer so that it hybridizes just down-stream of the stop codon, but still includes the C-terminus of the ORF. Note that you will need to replace the stop codon with a codon for an innocuous amino acid such as glycine, alanine, or lysine (see below).
Example #2 of Reverse Primer Design
Below is the sequence for the C-terminus of a theoretical protein. The stop codon is underlined.
To fuse the ORF in frame with a C-terminal tag, remove the stop codon by starting with nucleotides homologous to the last codon (TGC) and continue upstream. The reverse primer will be:
This will amplify the C-terminus without the stop codon and allow you to join the ORF in frame with a C-terminal tag.
If you don't want to join the ORF in frame with a C-terminal tag, simply design the reverse primer to include the stop codon.
Remember that the pcDNA6.2/GeneBLAzer-GW/D-TOPO® vectors accept blunt-end PCR products.
Do not add 5′ phosphates to your primers for PCR. This will prevent ligation into the pcDNA6.2/GeneBLAzer-GW/D-TOPO® vectors.
We recommend that you gel-purify your oligonucleotides, especially if they are long (>30 nucleotides).
Cloning into pcDNA6.2/cGeneBLAzer-GW/D-TOPO®
Introduction
pcDNA6.2/cGeneBLAzer-GW/D-TOPO® allows expression of recombinant proteins containing a C-terminal β-lactamase reporter; however, you may use this vector to express native proteins or C-terminal fusion proteins. You may also use this vector in the Tag-On-Demand™ System.
Kozak Consensus Sequence
Your sequence of interest should contain a Kozak translation initiation sequence with an ATG initiation codon for proper initiation of translation (Kozak, M. (1987). An Analysis of 5′-Noncoding Sequences from 699 Vertebrate Messenger RNAs. Nucleic Acids Res. 15, 8125-8148; Kozak, M. (1991). An Analysis of Vertebrate mRNA Sequences: Intimations of Translational Control. J. Cell Biology 115, 887-903; Kozak, M. (1990). Downstream Secondary Structure Facilitates Recognition of Initiator Codons by Eukaryotic Ribosomes. Proc. Natl. Acad. Sci. USA 87, 8301-8305). An example of a Kozak consensus sequence is provided below. The ATG initiation codon is shown underlined.
Other sequences are possible, but the G or A at position −3 and the G at position +4 are the most critical for function.
Additional Cloning Considerations
Consider the following when designing PCR primers to clone your DNA into pcDNA6.2/cGeneBLAzer-GW/D-TOPO®.
For all cases, design the forward PCR primer such that the ATG initiation codon is in the context of a Kozak consensus sequence (see above) and directly follows the 5′ CACC overhang. To design the reverse PCR primer, consider the following:
TOPO® Cloning Site of pcDNA6.2/cGeneBLAzer-GW/D-TOPO®
Use
Cloning into pcDNA6.2/nGeneBLAzer-GW/D-TOPO®
Introduction
pcDNA6.2/nGeneBLAzer-GW/D-TOPO® allows expression of recombinant proteins containing an N-terminal β-lactamase reporter and a C-terminal V5 epitope tag, if desired, and contains an ATG initiation codon within the context of a Kozak consensus sequence. You may use this vector in the Tag-On-Demand™ System.
TOPO® Cloning Site of pcDNA62/nGeneBLAzer-GW/D-TOPO®
Use
Producing Blunt-End PCR Products
Introduction
Once you have decided on a PCR strategy and have synthesized the primers, you are ready to produce your blunt-end PCR product using any thermostable, proofreading polymerase. Follow the guidelines below to produce your blunt-end PCR product.
Materials Needed
You should have the following materials on hand before beginning.
Note: dNTPs (adjusted to pH 8) are provided in the kit.
Thermocycler and thermostable, proofreading polymerase
10×PCR buffer appropriate for your polymerase
DNA template and primers for PCR product
Producing PCR Products
Set up a 25 μl or 50 μl PCR reaction using the guidelines below:
Follow the instructions and recommendations provided by the manufacturer of your thermostable, proofreading polymerase to produce blunt-end PCR products.
Use the cycling parameters suitable for your primers and template. Make sure to optimize PCR conditions to produce a single, discrete PCR product.
Use a 7 to 30 minute final extension to ensure that all PCR products are completely extended.
After cycling, place the tube on ice or store at −20° C. for up to 2 weeks. Proceed to Checking the PCR Product, below.
Checking the PCR Product
After you have produced your blunt-end PCR product, use agarose gel electrophoresis to verify the quality and quantity of your PCR product. Check for the following outcomes below.
Be sure you have a single, discrete band of the correct size. If you do not have a single, discrete band, follow the manufacturer's recommendations for optimizing your PCR with the polymerase of your choice. Alternatively, you may gel-purify the desired product.
Estimate the concentration of your PCR product. You will use this information when setting up your TOPO® Cloning reaction.
Performing the TOPO® Cloning Reaction
Introduction
Once you have produced the desired PCR product, you are ready to TOPO® Clone it into a pcDNA6.2/GeneBLAzer-GW/D-TOPO® vector and transform the recombinant vector into Mach1™-T1R cells.
Amount of PCR Product to Use in the TOPO® Cloning Reaction
When performing directional TOPO® Cloning, we have found that the molar ratio of PCR product:TOPO® vector used in the reaction is critical to its success. To obtain the highest TOPO® Cloning efficiency, use a 0.5:1 to 2:1 molar ratio of PCR product:TOPO® vector (see
Tip: For the pcDNA6.2/GeneBLAzer-GW/D-TOPO® vectors, using 1-5 ng of a 1 kb PCR product or 5-10 ng of a 2 kb PCR product in a TOPO® Cloning reaction generally results in a suitable number of colonies.
Using Salt Solution in the TOPO® Cloning Reaction
You will perform TOPO® Cloning in a reaction buffer containing salt (i.e. using the stock salt solution provided in the kit). Note that the amount of salt added to the TOPO® Cloning reaction varies depending on whether you plan to transform chemically competent cells (provided) or electrocompetent cells.
If you are transforming chemically competent E. coli, use the stock Salt Solution as supplied and set up the TOPO® Cloning reaction as directed below.
If you are transforming electrocompetent E. coli, the amount of salt in the TOPO®Cloning reaction must be reduced to 50 mM NaCl, 2.5 mM MgCl2 to prevent arcing during electroporation. Dilute the stock Salt Solution 4-fold with water to prepare a 300 mM NaCl, 15 mM MgCl2 Dilute Salt Solution. Use the Dilute Salt Solution to set up the TOPO® Cloning reaction as directed below.
Performing the TOPO® Cloning Reaction
Use the procedure below to perform the TOPO® Cloning reaction. Set up the TOPO® Cloning reaction depending on whether you plan to transform chemically competent E. coli or electrocompetent E. coli. Reminder: For optimal results, be sure to use a 0.5:1 to 2:1 molar ratio of PCR product:TOPO® vector in your TOPO® Cloning reaction.
Note: The blue color of the TOPO® vector solution is normal and is used to visualize the solution.
E. coli
E. coli
Mix reaction gently and incubate for 5 minutes at room temperature (22-23° C.).
Note: For most applications, 5 minutes will yield a sufficient number of colonies for analysis. Depending on your needs, the length of the TOPO® Cloning reaction can be varied from 30 seconds to 30 minutes. For routine subcloning of PCR products, 30 seconds may be sufficient. For large PCR products (>1 kb) or if you are TOPO® Cloning a pool of PCR products, increasing the reaction time may yield more colonies.
Place the reaction on ice and proceed to Transforming One Shot® Mach1™-T1R Competent Cells.
Note: You may store the TOPO® Cloning reaction at −20° C. overnight.
Transforming One Shot® Mach1™-T1R Competent Cells
Introduction
Once you have performed the TOPO® Cloning reaction, you will transform your
GeneBLAzer™ Directional TOPO® construct into competent E. coli. One Shot® Mach1™-T1R Chemically Competent E. coli (Box 2) are included to facilitate transformation, however, you may also transform other chemically competent cells (e.g. TOP10) or electrocompetent cells. Protocols to transform chemically competent or electrocompetent E. coli are provided in this section.
Blasticidin Selection
The presence of the EM7 promoter and the Blasticidin resistance gene in the pcDNA6.2/GeneBLAzer-GW/-D-TOPO® vectors allows for selection of E. coli transformants using Blasticidin. For selection, use Low Salt LB agar plates containing 100 μg/ml Blasticidin. For Blasticidin to be active, the salt concentration of the medium must remain low (<90 mM) and the pH must be 7.0.
Blasticidin is available separately from Invitrogen.
The Mach1™-T1R strain allows you to visualize colonies 8 hours after plating on ampicillin selective plates. If you are using Blasticidin selection, you will need to incubate plates overnight in order to visualize colonies.
With the Mach1™-T1R strain, you may also prepare plasmid DNA 4 hours after inoculating a single, overnight-grown colony. Note that you will get sufficient growth of transformed cells within 4 hours with either ampicillin or Blasticidin selection.
Materials Needed
You should have the following materials on hand before beginning:
TOPO® Cloning reaction from Performing the TOPO® Cloning Reaction, Step 2
S.O.C. medium (included with the kit)
42° C. water bath (or electroporator with cuvettes, optional)
LB plates containing 100 μg/ml ampicillin or Low Salt LB plates containing 100 μg/ml Blasticidin (two for each transformation)
37° C. shaking and non-shaking incubator
There is no blue-white screening for the presence of inserts. Most transformants will contain recombinant plasmids with the PCR product of interest cloned in the correct orientation. Sequencing primers are included in the kit to sequence across an insert in the multiple cloning site to confirm orientation and reading frame.
Preparing for Transformation
For each transformation, you will need one vial of competent cells and two selective plates.
Equilibrate a water bath to 42° C. (for chemical transformation) or set up your electroporator if you are using electrocompetent E. coli.
Warm the vial of S.O.C. medium from Box 2 to room temperature.
Warm selective plates at 37° C. for 30 minutes.
Thaw on ice 1 vial of One Shoe Mach1™-T1R cells from Box 2 for each transformation.
If you are using ampicillin selection and wish to visualize colonies within 8 hours of plating, it is essential that you prewarm your LB plates containing 100 μg/ml ampicillin prior to spreading.
One Shot® Mach1™-T1R Chemical Transformation Protocol
Add 2 μl of the TOPO® Cloning reaction from Performing the TOPO® Cloning Reaction into a vial of One Shot® Mach1™-T1R Chemically Competent E. coli and mix gently. Do not mix by pipetting up and down.
Incubate on ice for 5 to 30 minutes.
Note: Longer incubations on ice seem to have a minimal effect on transformation efficiency. The length of the incubation is at the user's discretion.
Heat-shock the cells for 30 seconds at 42° C. without shaking.
Immediately transfer the tubes to ice.
Add 250 μl of room temperature S.O.C. medium.
Cap the tube tightly and shake the tube horizontally (200 rpm) at 37° C. for 1 hour.
Spread 50-200 μl from each transformation on a prewarmed selective plate. We recommend plating two different volumes to ensure that at least one plate will have well-spaced colonies.
Incubate plates at 37° C. If you are using ampicillin selection, visible colonies should appear within 8 hours. For Blasticidin selection, incubate plates overnight.
An efficient TOPO® Cloning reaction should produce several hundred colonies. Pick ˜5 colonies for analysis.
Transformation by Electroporation
Use ONLY electrocompetent cells for electroporation to avoid arcing. Do not use the One Shot® Mach1-T1R chemically competent cells for electroporation.
Add 2 μl of the TOPO® Cloning reaction from Performing the TOPO® Cloning
Reaction into a sterile microcentrifuge tube containing 50 μl of electrocompetent E. coli and mix gently. Do not mix by pipetting up and down. Avoid formation of bubbles. Transfer the cells to a 0.1 cm cuvette.
Electroporate your samples using your own protocol and your electroporator.
Note: If you have problems with arcing, see below.
Immediately add 250 μl of room temperature S.O.C. medium.
Transfer the solution to a 15 ml snap-cap tube (e.g. Falcon) and shake for at least 1 hour at 37° C. to allow expression of the ampicillin resistance gene.
Spread 20-100 μl from each transformation on a prewarmed selective plate and incubate overnight at 37° C. To ensure even spreading of small volumes, add 20 μl of S.O.C. medium. We recommend that you plate two different volumes to ensure that at least one plate will have well-spaced colonies.
An efficient TOPO® Cloning reaction may produce several hundred colonies. Pick ˜5 colonies for analysis.
To prevent arcing of your samples during electroporation, the volume of cells should be between 50 and 80 μl (0.1 cm cuvettes) or 100 to 200 μl (0.2 cm cuvettes).
If you experience arcing during transformation, try one of the following suggestions:
Reduce the voltage normally used to charge your electroporator by 10%
Reduce the pulse length by reducing the load resistance to 100 ohms
Ethanol precipitate the TOPO® Cloning reaction and resuspend in water prior to electroporation
Analyzing Transformants
Analyzing Positive Clones
Pick 5 colonies and culture them overnight in LB or SOB medium containing 50-100 μg/ml ampicillin.
2. Isolate plasmid DNA using your method of choice. If you need ultra-pure plasmid DNA for automated or manual sequencing, we recommend using the PureLink™ HQ Mini Plasmid Purification Kit (Catalog no. K2100-01).
3. Analyze the plasmids by restriction analysis to confirm the presence and correct orientation of the insert. Use a restriction enzyme or a combination of enzymes that cut once in the vector and once in the insert.
Sequencing Primers for pcDNA6.2/cGeneBLAzer-GW/D-TOPO®
To confirm that your gene of interest is in frame with the bla(M) reporter gene, you may sequence your construct, if desired. Keep the following in mind when designing your sequencing primers:
Use a forward primer which hybridizes within the 3′ end of your gene of interest to sequence through the 5′ region of the bla(M) reporter gene.
Do not use a reverse primer that hybridizes within the bla(M) reporter gene. Any primer that hybridizes within the bla(M) reporter gene will also hybridize within the ampicillin resistance gene, contaminating your results.
Note: Because you will not be using a reverse primer, you will only be able to sequence the sense strand of your construct.
Use the T7 Promoter primer (supplied with Catalog nos. 12578-076 and 12578-084) to sequence through the 5′ region of your gene of interest.
Sequencing Primers for pcDNA6.2/n GeneBLAzer-GW/D-TOPO®
To confirm that your gene of interest is in frame with the bla(M) reporter gene or the V5 epitope tag, you may sequence your construct, if desired. Keep the following in mind when designing your sequencing primers:
Use a reverse primer which hybridizes within the 5′ end of your gene of interest to sequence through the 3′ region of the bla(M) reporter gene.
Do not use a forward primer that hybridizes within the bla(M) reporter gene. Any primer that hybridizes within the β-lactamase reporter gene will also hybridize within the ampicillin resistance gene, contaminating your results.
Note: Because you will not be using a forward primer, you will only be able to sequence the anti-sense strand of your construct.
Use the TK polyA Reverse primer (supplied with Catalog nos. 12578-092 and 12578-100) to sequence through the V5 epitope.
If you download the sequence for pcDNA6.2/cGeneBLAzer-GW/D-TOPO® or pcDNA6.2/cGeneBLAzer-GW/D-TOPO® from our Web site, note that the overhang sequence (GTGG) will be shown already hybridized to CACC. No DNA sequence analysis program allows us to show the overhang without the complementary sequence.
Analyzing Transformants by PCR
You may analyze positive transformants using PCR. If you are using pcDNA6.2/cGeneBLAzer-GW/D-TOPO®, use a combination of the T7 Promoter primer and a primer that hybridizes within your insert. If you are using pcDNA6.2/nGeneBLAzer-GW/D-TOPO®, use a combination of the TK polyA Reverse primer and a primer that hybridizes within your insert.
You will have to determine the amplification conditions. If you are using this technique for the first time, we recommend performing restriction analysis in parallel. Artifacts may be obtained because of mispriming or contaminating template. The protocol below is provided for your convenience. Other protocols are suitable.
Materials Needed
PCR SuperMix High Fidelity (Invitrogen, Catalog no. 10790-020) Appropriate forward and reverse PCR primers (20 μM each)
Procedure
1. For each sample, aliquot 48 μl of PCR SuperMix High Fidelity into a 0.5 ml microcentrifuge tube. Add 1 μl each of the forward and reverse PCR primer.
2. Pick 5 colonies and resuspend them individually in 50 μl of the PCR cocktail from Step 1, above.
3. Incubate reaction for 10 minutes at 94° C. to lyse cells and inactivate nucleases.
4. Amplify for 20 to 30 cycles.
5. For the final extension, incubate at 72° C. for 10 minutes. Store at +4° C.
6. Visualize by agarose gel electrophoresis.
Long-Term Storage
Once you have identified the correct clone, be sure to purify the colony and make a glycerol stock for long-term storage. We recommend that you store a stock of plasmid DNA at −20° C.
Streak the original colony out for single colony on LB plates containing 50-100 μg/ml ampicillin.
Isolate a single colony and inoculate into 1-2 ml of LB containing 50-100 μg/ml ampicillin.
Grow until culture reaches stationary phase.
Mix 0.85 ml of culture with 0.15 ml of sterile glycerol and transfer to a cryovial.
Store at −80° C.
Transfecting Cells
Introduction
This section provides general information to transfect your expression clone into the mammalian cell line of choice. We recommend that you include a positive control vector (pcDNA™6.2/cGeneBLAzer™-GW/lacZ or pcDNA™6.2/nGeneBLAzer™-GW/lacZ) and a mock transfection (negative control) in your experiments to evaluate your results.
If you plan to detect β-lactamase reporter activity in vivo using the GeneBLAzer™ In Vivo Detection Kit (supplied with Catalog nos. 12578-084 and 12578-100 only), note that a number of factors including cell type and cell density can influence the degree of the fluorescence signal detected. We recommend taking these factors into account when designing your transfection experiment.
Plasmid Preparation
Once you have generated your expression clone, you must isolate plasmid DNA for transfection. Plasmid DNA for transfection into eukaryotic cells must be very clean and free from phenol and sodium chloride. Contaminants will kill the cells, and salt will interfere with lipid complexing, decreasing transfection efficiency. We recommend isolating plasmid DNA using the PureLink™ HQ Mini Plasmid Purification Kit (Catalog no. K2100-01) or CsCl gradient centrifugation.
Positive Control
pcDNA™6.2/cGeneBLAzer™-GW/lacZ or pcDNA™6.2/nGeneBLAzer™-GW/lacZ is provided as a positive control vector for mammalian cell transfection and expression and may be used to optimize recombinant protein expression levels in your cell line. These vectors allow expression of the β-galactosidase gene with either an N-terminal or C-terminal fusion to the β-lactamase reporter.
To Propagate and Maintain the Plasmid:
Use the stock solution to transform a recA, endA E. coli strain like Mach1™, TOP10, DH5α™, or equivalent.
Select transformants on LB agar plates containing 50-100 μg/ml ampicillin.
Prepare a glycerol stock of a transformant containing plasmid for long-term storage.
Methods of Transfection
For established cell lines (e.g. HeLa), consult original references or the supplier of your cell line for the optimal method of transfection. We recommend that you follow exactly the protocol for your cell line. Pay particular attention to medium requirements, when to pass the cells, and at what dilution to split the cells. Further information is provided in Current Protocols in Molecular Biology (Ausubel, F. M., Brent, R., Kingston, R. E., Moore, D. D., Seidman, J. G., Smith, J. A., and Struhl, K. (1994). Current Protocols in Molecular Biology (New York: Greene Publishing Associates and Wiley-Interscience)).
Methods for transfection include calcium phosphate (Chen, C., and Okayama, H. (1987). High-Efficiency Transformation of Mammalian Cells by Plasmid DNA. Mol. Cell. Biol. 7, 2745-2752; Wigler, M., Silverstein, S., Lee, L.-S., Pellicer, A., Cheng, Y.-C., and Axel, R. (1977). Transfer of Purified Herpes Virus Thymidine Kinase Gene to Cultured Mouse Cells. Cell 11, 223-232), lipid-mediated (Feigner, P. L., Holm, M., and Chan, H. (1989). Cationic Liposome Mediated Transfection. Proc. West. Pharmacol. Soc. 32, 115-121; Feigner, P. L. a., and Ringold, G. M. (1989). Cationic Liposome-Mediated Transfection. Nature 337, 387-388) and electroporation (Chu, G., Hayakawa, H., and Berg, P. (1987). Electroporation for the Efficient Transfection of Mammalian Cells with DNA. Nucleic Acids Res. 15, 1311-1326; Shigekawa, K., and Dower, W. J. (1988). Electroporation of Eukaryotes and Prokaryotes: A General Approach to the Introduction of Macromolecules into Cells. BioTechniques 6, 742-751). For high efficiency transfection in a broad range of mammalian cell lines, we recommend using Lipofectamine™ 2000 Reagent (Catalog no. 11668-027) available from Invitrogen.
Creating Stable Cell Lines
Introduction
The GeneBLAzer™ Directional TOPO® vectors contain the Blasticidin resistance gene to allow selection of stable cell lines. If you wish to create stable cell lines, transfect your construct into the mammalian cell line of choice and select for foci using Blasticidin. General information and guidelines are provided below.
To obtain stable transfectants, we recommend that you linearize your pcDNA6.2/GeneBLAzer-GW/D-TOPO® construct before transfection. While linearizing the vector may not improve the efficiency of transfection, it increases the chances that the vector does not integrate in a way that disrupts elements necessary for expression in mammalian cells. To linearize your construct, cut at a unique site that is not located within a critical element or within your gene of interest.
Determining Blasticidin Sensitivity
To successfully generate a stable cell line expressing your protein of interest, you need to determine the minimum concentration of Blasticidin required to kill your untransfected host cell line by performing a kill curve experiment (see below). Typically, concentrations ranging from 2.5 to 10 μg/ml Blasticidin are sufficient to kill most untransfected mammalian cell lines. Blasticidin is available separately from Invitrogen (Catalog no. R210-01).
Plate cells at approximately 25% confluence. Prepare a set of 6 plates.
On the following day, replace the growth medium with fresh growth medium containing varying concentrations of Blasticidin (e.g. 0, 1, 3, 5, 7.5, and 10 μg/ml Blasticidin).
Replenish the selective media every 3-4 days, and observe the percentage of surviving cells.
Count the number of viable cells at regular intervals to determine the appropriate concentration of Blasticidin that prevents growth within 10-14 days after addition of Blasticidin.
Generating Stable Cell Lines
Once you have determined the appropriate Blasticidin concentration to use for selection, you can generate a stable cell line expressing your pcDNA6.2/GeneBLAzer-GW/D-TOPO® construct.
Transfect the mammalian cell line of interest with the pcDNA6.2/cGeneBLAzer-GW/D-TOPO® or pcDNA6.2/nGeneBLAzer-GW/D-TOPO® construct using your transfection method of choice.
24 hours after transfection, wash the cells and add fresh growth medium.
48 hours after transfection, split the cells into fresh growth medium such that they are no more than 25% confluent. If the cells are too dense, the antibiotic will not kill the cells. Antibiotics work best on actively dividing cells.
Incubate the cells at 37° C. for 2-3 hours until they have attached to the culture dish.
Remove the growth medium and replace with fresh growth medium containing Blasticidin at the predetermined concentration required for your cell line.
Feed the cells with selective media every 3-4 days until Blasticidin-resistant colonies can be identified.
Pick at least 5 Blasticidin-resistant colonies and expand them to assay for recombinant protein expression.
Detecting Recombinant Fusion Proteins
Introduction
Depending on the kit you are using, you will assay for β-lactamase reporter activity through in vivo or in vitro detection methods. A brief description of each detection method is provided below. For detailed information, refer to the GeneBLAzer™ Detection Kits manual. If you have generated a pcDNA6.2/nGeneBLAzer-GW/D-TOPO® construct that contains your gene of interest fused to the V5 epitope tag, you may also detect your recombinant fusion protein by Western blot analysis using one of the Anti-V5 Antibodies available from Invitrogen.
In Vitro Detection
Using the GeneBLAzer™ In Vitro Detection Kit allows you to quantitate the amount of intracellular β-lactamase in cells based on the β-lactamase activity in lysates.
To detect β-lactamase activity in mammalian cell lysates, you will use the CCF2-FA substrate. CCF2-FA is the non-esterified, free acid form of CCF2, and is recommended for in vitro use because it is readily soluble in aqueous solution and may be added directly to pre-made cell lysates. Once added to cell lysates, you may quantitate the CCF2-FA fluorescence signal using a fluorescence plate reader or a fluorometer.
To prepare cell lysates from mammalian cells containing the bla(M) reporter gene, you must use a method that will preserve the activity of the β-lactamase enzyme. Refer to the GeneBLAzer™ Detection Kits manual for detailed guidelines and protocols to prepare CCF2-FA solution, prepare cell lysates and samples, and detect CCF2 signal.
In Vivo Detection
Using the GeneBLAzer™ In Vivo Detection Kit allows you to measure β-lactamase reporter activity in live mammalian cells. Once β-lactamase reporter activity has been measured, cells may be cultured further for use in additional assays or other downstream applications.
To detect β-lactamase activity in live mammalian cells, you will use the CCF2-AM substrate. CCF2-AM is the membrane-permeable, esterified form of CCF2, and is recommended for in vivo use because it is non-toxic, lipophilic, and readily enters the cell. Once cells are “loaded” with CCF2-AM, you may quantitate the CCF2 fluorescence signal using a variety of methods.
Refer to the GeneBLAzer™ Detection Kits manual for detailed guidelines and protocols to prepare CCF2-AM solution, load cells with CCF2-AM substrate, and detect CCF2 signal.
Detecting the V5 Epitope Tag
If you are using pcDNA6.2/nGeneBLAzer-GW/D-TOPO® vector and you have fused your gene of interest to the V5 epitope tag, you may detect expression of your recombinant fusion protein using the Anti-V5 Antibody (Catalog no. R960-25), Anti-V5-HRP Antibody (Catalog no. R961-25), or Anti-V5-AP Antibody (Catalog no. R962-25) available from Invitrogen. In addition, the Positope™ Control Protein (Catalog no. R900-50) is available from Invitrogen for use as a positive control for detection of fusion proteins containing a V5 epitope. The ready-to-use WesternBreeze® Chromogenic Kits and WesternBreeze® Chemiluminescent Kits are available from Invitrogen to facilitate detection of antibodies by colorimetric or chemiluminescent methods.
Expression of your protein fused to the β-lactamase reporter and/or to the V5 epitope tag will increase the size of your recombinant protein. The table below lists the increase in the molecular weight of your recombinant protein that you should expect from a particular fusion. Note that the expected sizes take into account any additional amino acids between the gene of interest and the fusion peptide.
Assay for β-Galactosidase
If you use pcDNA™6.2/cGeneBLAzer™-GW/lacZ or pcDNA™6.2/nGeneBLAzer™-GW/lacZ) as a positive control vector, you may assay for β-galactosidase expression by Western blot analysis or activity assay (Miller, J. H. (1972). Experiments in Molecular Genetics (Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory). Invitrogen offers β-Gal Antiserum, the O-Gal Assay Kit, and the β-Gal Staining Kit for fast and easy detection of β-galactosidase expression.
Creating an Entry Clone
Introduction
Once you have TOPO® Cloned your gene of interest into a GeneBLAzer™ Directional TOPO® vector, you may perform a BP recombination reaction between your expression construct and a Gateway® donor vector to generate an entry clone. Once you generate an entry clone, your gene of interest may then be easily shuttled into a large selection of destination vectors using the LR recombination reaction. To ensure that you obtain the best possible results, we recommend that you read this section and the next section entitled Performing the BP Recombination Reaction before beginning.
Recombining the Expression Clone with a Donor Vector
Before performing the BP recombination reaction, consider the following points:
The bla(M) reporter gene will not be recombined into the entry clone. If you are using pcDNA6.2/nGeneBLAzer-GW/D-TOPO®, the V5 epitope tag will also not be recombined into the entry clone. If you wish to fuse your gene of interest to any N-terminal or C-terminal peptides, the peptides will need to be provided by the destination vector in the LR recombination reaction.
If you cloned the gene of interest to be in frame with an N-terminal or C-terminal peptide in one of the GeneBLAzer™ Directional TOPO® vectors, the gene will remain in frame with any N-terminal or C-terminal tags provided by the destination vector following the LR recombination reaction.
Depending on the design of your forward and reverse primers, your gene in the entry clone may not contain an ATG initiation codon within the context of a Kozak consensus sequence or a stop codon. If either of these are required, they will need to be provided by the destination vector in the LR recombination reaction.
Experimental Outline
To generate an entry clone, you will:
Perform a BP recombination reaction between your pcDNA6.2/GeneBLAzer-GW/D-TOPO® expression clone and an attP-containing donor vector (see below)
Transform the reaction mixture into a suitable E. coli host
Select for Entry Clones
Gateway® Donor Vectors
Invitrogen offers a variety of Gateway® donor vectors to help you generate an entry clone containing your gene of interest.
For optimal efficiency, perform the BP recombination reaction using:
Linear pcDNA6.2/GeneBLAzer-GW/D-TOPO® expression clone (see below for guidelines to linearize expression clones)
Supercoiled attP-containing donor vector
Note: Supercoiled or relaxed attB expression clones may be used, but will react less efficiently than linear attB expression clones.
Linearizing Expression Clones
We recommend that you linearize your pcDNA6.2/GeneBLAzer-GW/D-TOPO® expression clone using a suitable restriction enzyme (see the guidelines below).
Linearize 1 to 2 μg of the expression clone with a unique restriction enzyme that does not digest within the gene of interest and is located outside the attB region.
Ethanol precipitate the DNA after digestion by adding 0.1 volume of 3 M sodium acetate followed by 2.5 volumes of 100% ethanol.
Pellet the DNA by centrifugation. Wash the pellet twice with 70% ethanol.
Dissolve the DNA in TE Buffer, pH 8.0 to a final concentration of 50-150 ng/μl.
Performing the BP Recombination Reaction
Introduction
General guidelines and instructions are provided in this section to perform a BP recombination reaction using your pcDNA6.2/GeneBLAzer-GW/D-TOPO® expression clone and a donor vector, and to transform the reaction mixture into a suitable E. coli host to select for entry clones. We recommend that you include a positive control (see below) in your experiment to help you evaluate your results.
Positive Control
pEXP7-tet is provided with the BP Clonase™ enzyme mix as a positive control for the BP reaction. pEXP7-tet is an approximately 1.4 kb linear fragment and contains attB sites flanking the tetracycline resistance gene and its promoter (Tcr). Using the pEXP7-tet fragment in a BP reaction with a donor vector results in entry clones that express the tetracycline resistance gene. The efficiency of the BP recombination reaction can easily be determined by streaking entry clones onto LB plates containing 20 μg/ml tetracycline.
Determining How Much DNA to Use
For optimal efficiency, we recommend using the following amounts of linearized attB expression clone and donor vector in a 20 μl BP recombination reaction:
An equimolar amount of linearized attB expression clone and the donor vector
100 femtomoles (fmol) each of linearized attB expression clone and donor vector is preferred, but the amount of attB expression clone used may range from 40-100 fmol
Note: 100 fmol of donor vector (pDONR™201, pDONR™221, or pDONR™/Zeo) is approximately 300 ng
For a formula to convert fmol of DNA to nanograms (ng), see below.
Do not use more than 500 ng of donor vector in a 20 μl BP reaction as this will affect the efficiency of the reaction
Do not exceed more than 1 μg of total DNA (donor vector plus attB expression clone) in a 20 μl BP reaction as excess DNA will inhibit the reaction
Converting Femtomoles (fmol) to Nanograms (ng)
Use the following formula to convert femtomoles (fmol) of DNA to nanograms (ng) of DNA:
where N is the size of the DNA in bp.
Example of fmol to ng Conversion
In this example, you need to use 100 fmol of your pcDNA6.2/GeneBLAzer-GW/D-TOPO® expression clone which is 7.5 kb in size in the BP reaction. Calculate the amount of your pcDNA6.2/GeneBLAzer-GW/D-TOPO® expression clone required for the reaction (in ng) by using the equation above:
Materials Needed
You should have the following materials on hand before beginning:
Linearized pcDNA6.2/GeneBLAzer-GW/D-TOPO® expression clone pDONR™ vector (resuspended to 150 ng/μl)
BP Clonase™ enzyme mix
5×BP Clonase Reaction Buffer (supplied with the BP Clonase™ enzyme mix)
pEXP7-tet positive control, optional (50 ng/μl; supplied with the BP Clonase™ enzyme mix)
TE Buffer, pH 8.0 (10 mm Tris-HCl, pH 8.0; 1 mM EDTA)
2 μg/ml Proteinase K solution (supplied with the BP Clonase™ enzyme mix; thaw and keep on ice until use)
Appropriate competent E. coli host and growth media for expression
S.O.C. medium
LB agar plates containing the appropriate antibiotic to select for entry clones
Setting Up the BP Recombination Reaction
Add the following components to 1.5 ml microcentrifuge tubes at room temperature and mix.
Note: To include a negative control, set up a second sample reaction and substitute TE Buffer, pH 8.0 for the BP Clonase™ enzyme mix (see Step 4).
Remove the BP Clonase™ enzyme mix from −80° C. and thaw on ice 2 minutes).
Vortex the BP Clonase™ enzyme mix briefly twice (2 seconds each time).
To each sample above, add 4 μl of BP Clonase™ enzyme mix. Mix well by vortexing briefly twice (2 seconds each time).
Reminder: Return BP Clonase™ enzyme mix to −80° C. immediately after use.
Incubate reactions at 25° C. for 1 hour.
Note: For most applications, a 1 hour incubation will yield a sufficient number of entry clones. Depending on your needs, the length of the recombination reaction can be extended up to 18 hours. An overnight incubation typically yields 5-10 times more colonies than a 1 hour incubation.
Add 2 μl of the Proteinase K solution to each reaction. Incubate for 10 minutes at 37° C.
Transform 1 μl of the BP recombination reaction into a suitable E. coli host (follow the manufacturer's instructions) and select for entry clones.
Note: You may store the BP reaction at −20° C. for up to 1 week before transformation,
if desired.
What You Should See
If you use E. coli cells with a transformation efficiency of 1×108 cfu/μg, the BP recombination reaction should give >1500 colonies if the entire BP reaction is transformed and plated.
Verifying pEXP7-tet Entry Clones
If you included the pEXP7-tet control in your experiments, you may access the efficiency of the BP reaction by streaking entry clones onto LB plates containing 20 μg/ml tetracycline. True entry clones should be tetracycline-resistant.
Troubleshooting
TOPO® Cloning Reaction and Transformation
The table below lists some potential problems and possible solutions that may help you troubleshoot the TOPO® Cloning and transformation reactions. To help evaluate your results, we recommend that you perform the control reactions in parallel with your samples.
E. coli at −80° C.
Performing the Control Reactions
Introduction
We recommend performing the following control TOPO® Cloning reactions the first time you TOPO® Clone to help you evaluate your results. Performing the control reactions involves producing a control PCR product using the reagents included in the kit and using this product directly in a TOPO® Cloning reaction.
Before Starting
For each transformation, prepare two LB plates containing 50-100 μg/ml ampicillin.
Producing the Control PCR Product
Use your thermostable, proofreading polymerase and the appropriate buffer to amplify the control PCR product. Follow the manufacturer's recommendations for the polymerase you are using.
1. To produce the 750 bp control PCR product, set up the following 50 μl PCR:
2. Overlay with 70 μl (1 drop) of mineral oil, if required.
3. Amplify using the following cycling parameters:
Remove 10 μl from the reaction and analyze by agarose gel electrophoresis. A discrete 750 bp band should be visible.
Estimate the concentration of the PCR product, and adjust as necessary such that the amount of PCR produce used in the control TOPO® Cloning reaction results in an optimal molar ratio of PCR product:TOPO® vector (i.e. 0.5:1 to 2:1). Proceed to Control TOPO® Cloning Reactions.
Performing the Control Reactions, Continued
Control TOPO® Cloning Reactions
Using the control PCR product produced and a pcDNA6.2/GeneBLAzer-GW/D-TOPO® vector, set up two 6 μl TOPO® Cloning reactions as described below. If you plan to transform electrocompetent E. coli, use Dilute Salt Solution in place of the Salt Solution.
Set up control TOPO® Cloning reactions:
Incubate at room temperature for 5 minutes and place on ice.
Transform 2μ of each reaction into separate vials of One Shot® Mach1™-T1R cells using the protocol.
Spread 50-200 μl of each transformation mix onto LB plates containing 50-100 μg/ml ampicillin. Be sure to plate two different volumes to ensure that at least one plate has well-spaced colonies.
Incubate overnight at 37° C.
Transformation Control
pUC19 plasmid is included to check the transformation efficiency of the One Shot® Mach1™-T1R competent cells. Transform one vial of One Shot® Mach1™-T1R cells with 10 pg of pUC19 using the protocol. Plate 10 μl of the transformation mixture plus 20 μl of S.O.C. medium on LB plates containing 100 μg/ml ampicillin. Transformation efficiency should be ˜1×109 cfu/μg DNA.
Analysis of Results
Hundreds of colonies from the vector +PCR insert reaction should be produced. To analyze the transformations, isolate plasmid DNA and digest with the appropriate restriction enzyme as listed below. Refer to the table below for expected digestion patterns.
Greater than 90% of the colonies should contain the 750 bp insert in the correct orientation. Relatively few colonies should be produced in the vector-only reaction.
Gel Purifying PCR Products
Introduction
Smearing, multiple banding, primer-dimer artifacts, or large PCR products (>3 kb) may necessitate gel purification. If you wish to purify your PCR product, be extremely careful to remove all sources of nuclease contamination. There are many protocols to isolate DNA fragments or remove oligonucleotides. Refer to Current Protocols in Molecular Biology, Unit 2.6 (Ausubel, F. M., Brent, R., Kingston, R. E., Moore, D. D., Seidman, J. G., Smith, J. A., and Struhl, K. (1994). Current Protocols in Molecular Biology (New York: Greene Publishing Associates and Wiley-Interscience) for the most common protocols. Three simple protocols are provided below.
The cloning efficiency may decrease with purification of the PCR product
(e.g. PCR product too dilute). You may wish to optimize your PCR to produce a single band (see Producing Blunt-End PCR Products).
Using the S.N.A.P.™ Gel Purification Kit
The S.N.A.P.™ Gel Purification Kit available from Invitrogen (Catalog no.
K1999-25) allows you to rapidly purify PCR products from regular agarose gels.
1. Electrophorese amplification reaction on a 1 to 5% regular TAE agarose gel.
Note: Do not use TBE to prepare agarose gels. Borate interferes with the sodium iodide step, below.
2. Cut out the gel slice containing the PCR product and melt it at 65° C. in 2 volumes of the 6 M sodium iodide solution.
3. Add 1.5 volumes Binding Buffer.
4. Load solution (no more than 1 ml at a time) from Step 3 onto a S.N.A.P.™ column. Centrifuge 1 minute at 3000×g in a microcentrifuge and discard the supernatant.
5. If you have solution remaining from Step 3, repeat Step 4.
6. Add 900 μl of the Final Wash Buffer.
7. Centrifuge 1 minute at full speed in a microcentrifuge and discard the flow-through.
8. Repeat Step 7.
9. Elute the purified PCR product in 40 μl of TE or sterile water. Use 4 μl for the TOPO® Cloning reaction and proceed.
Quick S.N.A.P.™ Method
An even easier method is to simply cut out the gel slice containing your PCR product, place it on top of the S.N.A.P.™ column bed, and centrifuge at full speed for 10 seconds. Use 1-2 μl of the flow-through in the TOPO® Cloning reaction. Be sure to make the gel slice as small as possible for best results.
Gel Purifying PCR Products, Continued
Low-Melt Agarose Method
If you prefer to use low-melt agarose, use the procedure below. Note that gel purification will result in a dilution of your PCR product and a potential loss of cloning efficiency.
1. Electrophorese as much as possible of your PCR reaction on a low-melt agarose gel (0.8 to 1.2%) in TAE buffer.
2. Visualize the band of interest and excise the band.
3. Place the gel slice in a microcentrifuge tube and incubate the tube at 65° C. until the gel slice melts.
4. Place the tube at 37° C. to keep the agarose melted.
5. Add 4 μl of the melted agarose containing your PCR product to the TOPO® Cloning reaction as described.
6. Incubate the TOPO® Cloning reaction at 37° C. for 5 to 10 minutes. This is to keep the agarose melted.
7. Transform 2 to 4 μl directly into One Shot® Mach1™-T1R cells.
The cloning efficiency may decrease with purification of the PCR product. You may wish to optimize your PCR to produce a single band.
Recipes
LB (Luria-Bertani) Medium and Plates
1.0% Tryptone
0.5% Yeast Extract
1.0% NaCl
pH 7.0
For 1 liter, dissolve 10 g tryptone, 5 g yeast extract, and 10 g NaCl in 950 ml deionized water.
Adjust the pH of the solution to 7.0 with NaOH and bring the volume up to 1 liter.
Autoclave on liquid cycle for 20 minutes at 15 psi. Allow solution to cool to 55° C. and add antibiotic (50-100 μg/ml ampicillin) if needed.
Store at room temperature or at +4° C.
LB Agar Plates
Prepare LB medium as above, but add 15 g/L agar before autoclaving.
Autoclave on liquid cycle for 20 minutes at 15 psi.
After autoclaving, cool to ˜55° C., add antibiotic (50-100 μg/ml of ampicillin), and pour into 10 cm plates.
Let harden, then invert and store at +4° C.
Low Salt LB Medium with Blasticidin
10 g Tryptone
5 g NaCl
5 g Yeast Extract
Combine the dry reagents above and add deionized, distilled water to 950 ml. Adjust pH to 7.0 with 1 N NaOH. Bring the volume up to 1 liter. For plates, add 15 g/L agar before autoclaving.
Autoclave on liquid cycle at 15 psi and 121° C. for 20 minutes.
Allow the medium to cool to at least 55° C. before adding the Blasticidin to 100 μg/ml final concentration.
Store plates at +4° C. in the dark. Plates containing Blasticidin are stable for up to 2 weeks.
Blasticidin
Blasticidin S HCl is a nucleoside antibiotic isolated from Streptomyces griseochromogenes which inhibits protein synthesis in both prokaryotic and eukaryotic cells (Takeuchi, S., Hirayama, K., Ueda, K., Sakai, H., and Yonehara, H. (1958). Blasticidin S, A New Antibiotic. The Journal of Antibiotics, Series A 11, 1-5; Yamaguchi, H., Yamamoto, C., and Tanaka, N. (1965). Inhibition of Protein Synthesis by Blasticidin S. I. Studies with Cell-free Systems from Bacterial and Mammalian Cells. J. Biochem (Tokyo) 57, 667-677). Resistance is conferred by expression of either one of two Blasticidin S deaminase genes: bsd from Aspergillus terreus (Kimura, M., Takatsuki, A., and Yamaguchi, I. (1994). Blasticidin S Deaminase Gene from Aspergillus terreus (BSD): A New Drug Resistance Gene for Transfection of Mammalian Cells. Biochim. Biophys. ACTA 1219, 653-659) or bsr from Bacillus cereus (Izumi, M., Miyazawa, H., Kamakura, T., Yamaguchi, I., Endo, T., and Hanaoka, F. (1991). Blasticidin S-Resistance Gene (bsr): A Novel Selectable Marker for Mammalian Cells. Exp. Cell Res. 197, 229-233). These deaminases convert Blasticidin S to a non-toxic deaminohydroxy derivative (Izumi, M., Miyazawa, H., Kamakura, T., Yamaguchi, I., Endo, T., and Hanaoka, F. (1991). Blasticidin S-Resistance Gene (bsr): A Novel Selectable Marker for Mammalian Cells. Exp. Cell Res. 197, 229-233).
Molecular Weight, Formula, and Structure
The formula for Blasticidin S is C17H26N8O5—HCl, and the molecular weight is 458.9. The diagram below shows the structure of Blasticidin.
Handling Blasticidin
Always wear gloves, mask, goggles, and protective clothing (e.g. a laboratory coat) when handling Blasticidin. Weigh out Blasticidin and prepare solutions in a hood.
Preparing and Storing Stock Solutions
Blasticidin may be obtained separately from Invitrogen (Catalog no. R210-01) in 50 mg aliquots. Blasticidin is soluble in water. Sterile water is generally used to prepare stock solutions of 5 to 10 mg/ml.
pcDNA6.2/cGeneBLAzer-GW/D-TOPO® (5900) contains the following elements. All features have been functionally tested.
Features of pcDNA6.2/nGeneBLAzer-GW/D-TOPO®
pcDNA6.2/nGeneBLAzer-GW/D-TOPO® (5945) contains the following elements. All features have been functionally tested.
Exemplary Product Instructions
The following example is intended to illustrate exemplary methods for carrying out the present invention. Variations on the methods set forth herein will be readliy appreciated by those skilled in the art. The information set forth in this or any other example should not be construed as limiting the scope of the invention described herein. All catalog numbers mentioned in this example refer to specific products and reagents available from Invitrogen Corporation, Carlsbad, Calif., 92008. The exemplary methods described in this example can be carried out using the products and reagents designated by the catalog numbers, or with equivalent products and reagents available from other sources.
Accessory Products
Additional Products Additional products that may be used with pENTR/GeneBLAzer™ are available from Invitrogen.
Gateway® Destination Vectors
A large selection of Gateway® destination vectors is available from Invitrogen to facilitate expression of your gene of interest in virtually any protein expression system.
Overview
Introduction
pENTR/GeneBLAzer™ is a Gateway® entry clone containing the β-lactamase gene. Following recombination with a mammalian Gateway® destination vector to generate an expression control, β lactamase activity can be detected in vivo or in vitro using GeneBLAzer™ Technology. Detection of β lactamase activity allows you to optimize transfection and expression studies, normalize for experimental variability, and provides a highly sensitive and accurate method to quantitate gene expression in mammalian cells.
Features of pENTR/GeneBLAZer™
pENTR/GeneBLAzer™ contains the following elements:
rrnB transcription termination sequences to prevent basal expression of the β-lactamase gene in E. coli
attL1 and attL2 sites for site-specific recombination of the entry clone with a Gateway® destination vector
Kozak consensus sequence for efficient translation initiation in eukaryotic systems
β-lactamase bla(M) gene for in vivo or in vitro fluorescence detection
Kanamycin resistance gene for selection in E. coli
pUC origin for high-copy replication and maintenance of the plasmid in E. coli
For a map of pENTR/GeneBLAzer™, refer to
The Gateway® Technology
Gateway® is a universal cloning technology that takes advantage of the site-specific recombination properties of bacteriophage lambda (Landy, 1989) to provide a rapid and highly efficient way to move your gene of interest into multiple vector systems. To express the bla(M) gene in mammalian cells using Gateway® Technology, simply:
Generate an expression clone by performing an LR recombination reaction between pENTR/GeneBLAzer™ and a mammalian Gateway® destination vector of choice.
Transfect your expression clone into the cell line of choice and assay for transient expression of the bla(M) gene. Generate a stable cell line, if desired.
Advantages of pENTR/GeneBLAzer™
Using pENTR/GeneBLAzer™ and the GeneBLAzer™ Technology as a control for gene expression in mammalian cells provides the following advantages:
β-lactamase activity is detectable in living mammalian cells using fluorescence microscopy.
Provides a ratiometric readout to minimize differences due to variability in cell number, substrate concentration, fluorescence intensity, and emission sensitivity.
Compatible with a wide variety of in vivo and in vitro applications including microplate-based transcriptional assays and flow cytometry.
Using a non-toxic substrate allows continued cell culturing after quantitative analysis.
The GeneBLAzer™ Technology
Components of the GeneBLAzer™ System
The GeneBLAzer™ System facilitates fluorescence detection of β-lactamase activity in mammalian cells, and consists of two major components:
The β-lactamase gene, bla(M), a truncated form of the E. coli bla gene.
A fluorescence resonance energy transfer (FRET)-enabled substrate, CCF2 to facilitate fluorescence detection of β lactamase activity. In the absence or presence of β lactamase activity, cells loaded with the CCF2 substrate fluoresce green or blue, respectively. Comparing the ratio of blue to green fluorescence in a population of live cells or in a cell extract of your sample to a negative control provides a means to quantitate gene expression.
β-Lactamase (bla) Gene
β-lactamase is the product encoded by the ampicillin (bla) resistance gene and is the bacterial enzyme that hydrolyzes penicillins and cephalosporins. The bla gene is present in many cloning vectors and allows ampicillin selection in E. coli. β lactamase enzyme activity is not found in mammalian cells.
bla(M) Gene
The GeneBLAzer™ Technology uses a modified bla gene for
expression in mammalian cells. This bla gene is derived from the E. coli TEM-1 gene present in many cloning vectors (Zlokarnik, G., Negulescu, P. A., Knapp, T. E., Mere, L., Burres, N., Feng, L., Whitney, M., Roemer, K., and Tsien, R. Y. (1998). Quantitation of Transcription and Clonal Selection of Single Living Cells with b-Lactamase as Reporter. Science 279, 84-88), and has been modified in the following ways:
72 nucleotides encoding the first 24 amino acids of β lactamase were deleted from the N-terminal region of the gene. These 24 amino acids comprise the bacterial periplasmic signal sequence, and deleting this region allows cytoplasmic expression of β-lactamase in mammalian cells.
The amino acid at position 24 was mutated from His to Asp to create an optimal Kozak sequence for optimal translation initiation.
This modified gene is named bla(M).
Note: The TEM-1 gene also contains 2 mutations (at nucleotide positions 452 and 753) that distinguish it from the bla gene in pBR322 (Sutcliffe, J. G. (1978). Nucleotide Sequence of the Ampicillin Resistance Gene of Escherichia coli Plasmid pBR322. Proc. Nat. Acad. Sci. USA 75, 3737-3741).
Methods
Creating an Expression Clone
Introduction
You will need to perform an LR recombination reaction to transfer the β-lactamase gene to your Gateway® destination vector of choice. To ensure that you obtain the best possible results, we recommend that you read this section and the next section entitled Performing the LR Recombination Reaction before beginning.
Resuspending pENTR/GeneBLAzer™
pENTR/GeneBLAzer™ is supplied as 10 μg of plasmid, lyophilized in TE, pH 8.0. To use, resuspend the vector in 100 μl of sterile water to a final concentration of 100 ng/μl.
Tag-On-Demand™ System
The bla(M) gene in pENTR/GeneBLAzer™ contains a TAG (amber stop) codon, making it compatible with the Tag-On-Demand™ System which allows expression of both native and C-terminally-tagged recombinant protein from the same expression construct.
The System is based on stop suppression technology originally developed by RajBhandary and colleagues (Capone, J. P., Sharp, P. A., and RajBhandary, U. L. (1985). Amber, Ochre and Opal Suppressor tRNA Genes Derived from a Human Serine tRNA Gene. EMBO J. 4, 213-221) and consists of a recombinant adenovirus expressing a tRNAser suppressor. Following an LR recombination reaction with pENTR/GeneBLAzer™ and a destination vector containing a C-terminal tag, the bla(M) gene in the resulting expression clone will retain the TAG stop codon and will be fused in frame to the C-terminal tag. When the expression clone is transfected into mammalian cells and the tRNAser suppressor supernatant is present, the stop codon will be translated as serine, allowing translation to continue and resulting in production of C terminally-tagged β lactamase protein.
Recombination Region
Note the following features:
The bla(M) gene contains a Kozak consensus sequence with an ATG initiation codon (shown underlined) for proper initiation of translation (Kozak, M. (1987). An Analysis of 5′-Noncoding Sequences from 699 Vertebrate Messenger RNAs. Nucleic Acids Res. 15, 8125-8148; Kozak, M. (1991). An Analysis of Vertebrate mRNA Sequences: Intimations of Translational Control. J. Cell Biology 115, 887-903; Kozak, M. (1990). Downstream Secondary Structure Facilitates Recognition of Initiator Codons by Eukaryotic Ribosomes. Proc. Natl. Acad. Sci. USA 87, 8301-830).
The bla(M) gene contains a TAG stop codon and may be used with the Tag-On-Demand™ System to facilitate expression of a C-terminally-tagged protein, if desired (see previous page for more information).
Note: The C-terminal tag must be provided by the destination vector in the LR recombination reaction.
Shaded regions correspond to DNA sequences transferred from the pENTR/GeneBLAzer™ entry clone into the destination vector following recombination.
Performing the LR Recombination Reaction
Introduction
This section provides guidelines and protocols to perform an LR recombination reaction, transform the reaction mixture into a suitable E. coli host (see below), and to select for an expression clone.
E. coli Host
You may use any recA, endA E. coli strain including TOP10, DH5α™, or equivalent for transformation. Do not transform the LR reaction mixture into E. coli strains that contain the F′ episome (e.g. TOP10F′). These strains contain the ccdA gene and will prevent negative selection of your ccdB-containing destination vector.
Materials Needed
You should have the following materials on hand before beginning:
pENTR/GeneBLAzer™ entry clone (resuspended to 100 ng/μl)
Destination vector of choice (150 ng/μl in TE, pH 8.0)
LR Clonase™ enzyme mix (Invitrogen, Catalog no. 11791-019; keep at −80° C. until immediately before use)
5×LR Clonase™ Reaction Buffer (supplied with the LR Clonase™ enzyme mix)
TE Buffer, pH 8.0 (10 mM Tris-HCl, pH 8.0, 1 mM EDTA)
2 μg/μl Proteinase K solution (supplied with the LR Clonase™ enzyme mix; thaw and keep on ice until use)
Appropriate competent E. coli host and growth media for expression
S.O.C. Medium
LB agar plates containing the appropriate antibiotic to select for expression clones
Introduction
Add the following components to 1.5 ml microcentrifuge tubes at room temperature and mix.
Note: To include a negative control, set up a second sample reaction and substitute TE Buffer, pH 8.0 for the LR Clonase™ enzyme mix (see Step 4).
Remove the LR Clonase™ enzyme mix from −80° C. and thaw on ice 2 minutes).
Vortex the LR Clonase™ enzyme mix briefly twice (2 seconds each time).
To each sample above, add 4 μl of LR Clonase™ enzyme mix. Mix well by pipetting up and down.
Reminder: Return LR Clonase™ enzyme mix to −80° C. immediately after use.
Incubate reactions at 25° C. for 1 hour.
Note: Extending the incubation time to 18 hours typically yields more colonies.
Add 2 μl of the Proteinase K solution to each reaction. Incubate for 10 minutes at 37° C.
Transform 1 μl of the LR recombination reaction into a suitable E. coli host (follow the manufacturer's instructions) and select for expression clones.
Note: You may store the LR reaction at −20° C. for up to 1 week before transformation, if desired.
What You Should See
If you use E. coli cells with a transformation efficiency of 1×108 cfu/μg, the LR reaction should give >5000 colonies if the entire LR reaction is transformed and plated.
You may sequence your expression clone to confirm the presence of the bla(M) gene, if desired. If your expression clone contains an ampicillin resistance gene, do not use primers that hybridize within the bla(M) gene as they will also hybridize within the ampicillin resistance gene, contaminating your results.
Transfecting Cells
Introduction
This section provides general information for transfecting your expression clone into the mammalian cell line of choice. We recommend that you include a mock transfection (negative control) in your experiments to help you evaluate your results.
If you plan to detect β-lactamase activity in vivo using the GeneBLAzer™ In
Vivo Detection Kit, note that a number of factors including cell type and cell density can influence the degree of the fluorescence signal detected. We recommend taking these factors into account when designing your transfection experiment. For more information, refer to the section entitled General Guidelines to Use the GeneBLAzer™ In Vivo Detection Kit in the GeneBLAzer™ Detection Kits manual.
Methods of Transfection
For established cell lines (e.g. HeLa), consult original references or the supplier of your cell line for the optimal method of transfection. We recommend that you follow exactly the protocol for your cell line. Pay particular attention to medium requirements, when to pass the cells, and at what dilution to split the cells. Further information is provided in Current Protocols in Molecular Biology (Ausubel, F. M., Brent, R., Kingston, R. E., Moore, D. D., Seidman, J. G., Smith, J. A., and Struhl, K. (1994). Current Protocols in Molecular Biology (New York: Greene Publishing Associates and Wiley-Interscience)).
Methods for transfection include calcium phosphate (Chen, C., and Okayama, H. (1987). High-Efficiency Transformation of Mammalian Cells by Plasmid DNA. Mol. Cell. Biol. 7, 2745-2752; Wigler, M., Silverstein, S., Lee, L.-S., Pellicer, A., Cheng, Y.-C., and Axel, R. (1977). Transfer of Purified Herpes Virus Thymidine Kinase Gene to Cultured Mouse Cells. Cell 11, 223-232), lipid-mediated (Feigner, P. L., Holm, M., and Chan, H. (1989). Cationic Liposome Mediated Transfection. Proc. West. Pharmacol. Soc. 32, 115-121; Feigner, P. L. a., and Ringold, G. M. (1989). Cationic Liposome-Mediated Transfection. Nature 337, 387-388) and electroporation (Chu, G., Hayakawa, H., and Berg, P. (1987). Electroporation for the Efficient Transfection of Mammalian Cells with DNA. Nucleic Acids Res. 15, 1311-1326; Shigekawa, K., and Dower, W. J. (1988). Electroporation of Eukaryotes and Prokaryotes: A General Approach to the Introduction of Macromolecules into Cells. BioTechniques 6, 742-751). For high efficiency transfection in a broad range of mammalian cell lines, we recommend using Lipofectamine™ 2000 Reagent (Catalog no. 11668-027) available from Invitrogen.
Detecting β-Lactamase Activity
Introduction
To use the GeneBLAzer™ In Vivo Detection Kit or the GeneBLAzer™ In Vitro Detection Kit to detect β lactamase activity, refer to the GeneBLAzer™ Detection Kits manual for detailed information and protocols. A brief description of each detection method is provided below.
In Vitro Detection
Using the GeneBLAzer™ In Vitro Detection Kit allows you to quantitate the amount of intracellular β-lactamase in cells based on the β-lactamase activity in lysates.
To detect β-lactamase activity in mammalian cell lysates, you will use the CCF2-FA substrate. CCF2-FA is the non-esterified, free acid form of CCF2, and is recommended for in vitro use because it is readily soluble in aqueous solution and may be added directly to pre-made cell lysates. Once added to cell lysates, you may quantitate the CCF2-FA fluorescence signal using a fluorescence plate reader or a fluorometer.
To prepare cell lysates from mammalian cells containing the bla(M) gene, you must use a method that will preserve the activity of the β-lactamase enzyme. Refer to the GeneBLAzer™ Detection Kits manual for detailed guidelines and protocols.
In Vivo Detection
Using the GeneBLAzer™ In Vivo Detection Kit allows you to measure β-lactamase activity in live mammalian cells. Once β-lactamase activity has been measured, cells may be cultured further for use in additional assays or other downstream applications.
To detect β-lactamase activity in live mammalian cells, you will use the CCF2-AM substrate. CCF2-AM is the membrane-permeable, esterified form of CCF2, and is recommended for in vivo use because it is non-toxic, lipophilic, and readily enters the cell. Once cells are “loaded” with CCF2-AM, you may quantitate the CCF2 fluorescence signal using a variety of methods.
Features of pENTR/GeneBLAzer™
Having now fully described the present invention in some detail by way of illustration and example for purposes of clarity of understanding, it will be obvious to one of ordinary skill in the art that the same can be performed by modifying or changing the invention within a wide and equivalent range of conditions, formulations and other parameters without affecting the scope of the invention or any specific embodiment thereof, and that such modifications or changes are intended to be encompassed within the scope of the appended claims
All publications, patents and patent applications mentioned in this specification are indicative of the level of skill of those skilled in the art to which this invention pertains, and are herein incorporated by reference to the same extent as if each individual publication, patent or patent application was specifically and individually indicated to be incorporated by reference.
This application claims the benefit of U.S. Provisional Patent Application Nos. 60/482,504, filed Jun. 26, 2003, 60/487,301, filed Jul. 16, 2003, and 60/511,634, filed Oct. 17, 2003, the contents of which are relied upon and incorporated by reference in their entireties.
| Number | Date | Country | |
|---|---|---|---|
| 60511634 | Oct 2003 | US | |
| 60487301 | Jul 2003 | US | |
| 60482504 | Jun 2003 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 13053040 | Mar 2011 | US |
| Child | 13540574 | US | |
| Parent | 12019785 | Jan 2008 | US |
| Child | 13053040 | US | |
| Parent | 10877952 | Jun 2004 | US |
| Child | 12019785 | US |
