Patent Application
20250171830
The present invention relates to the field of nucleic acid hybridization probes.
The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Apr. 24, 2019, is named ENZ-117-PCT-SL_ST25.txt and is 3,603 bytes in size.
In situ hybridization (ISH) involves the hybridization of a labeled complementary DNA, RNA or modified nucleic acid strand, i.e., a nucleic acid probe, to a specific DNA or RNA sequence that may be present in a tissue or cell specimen and the detection of the hybridized probe. Probes are commonly labeled with haptens for affinity-based, enzyme-mediated colorimetric detection, or fluorescent moieties for direct fluorescent detection (so-called fluorescence in situ hybridization: “FISH”), or radioactively labeled. Human papillomavirus (HPV) infection is a well-established risk factor for the development of cervical carcinomas and precancerous lesions and, in recent years, the use of in situ hybridization for the detection of HPV genes or transcripts in human cervical cell specimens has been adopted.
What is needed and provided by the present invention are improved nucleic acid hybridization probes for in situ hybridization applications.
One embodiment of the invention provides a non-naturally occurring linear nucleic acid molecule having a S′ end and a 3′ end, which includes:
Another embodiment of the invention provides a non-naturally occurring linear nucleic acid molecule having a 5′ end and a 3′ end, which includes:
A further embodiment of the invention provides an in vitro hybrid composition of matter that includes:
A still further embodiment of the invention provides a method for detecting a target nucleic acid sequence in a sample that includes the steps of:
Another embodiment of the invention provides a method for preparing a nucleic acid hybridization probe composition for a nucleic acid target of interest that includes the steps of
A further embodiment of the invention provides a method for preparing a nucleic acid hybridization probe composition for a nucleic acid target of interest that includes the steps of:
Still another embodiment of the invention provides a method for preparing a nucleic acid hybridization probe composition that includes the steps of:
In any of the embodiments of the invention and variations thereof described herein, the series of first nucleic acid segments may, for example, include at least 2, at least 3, at least 4, or at least 5 first nucleic acid segments. In any of the embodiments of the invention and variations thereof described herein, the series of first nucleic acid segments may, for example, include in the range of 2-30 first nucleic acid segments or any subrange or whole number of first nucleic acid segments therein. In any of the embodiments of the invention and variations thereof described herein, the series of first nucleic acid segments may, for example, include in the range of 3-30 first nucleic acid segments or any subrange or whole number of first nucleic acid segments therein.
Additional features, advantages, and embodiments of the invention may be set forth or apparent from consideration of the following detailed description, drawings if any, and claims. Moreover, it is to be understood that both the foregoing summary of the invention and the following detailed description are exemplary and intended to provide further explanation without limiting the scope of the invention as claimed.
In one aspect, the invention provides nucleic acid hybridization probes having improved detectability. In one embodiment, the probes include a plurality of first segments sequentially complementary to a target nucleic acid sequence and, between neighboring first segments, a nucleic acid spacer segment which is not complementary to the target nucleic acid sequence and not complementary to the first segments, and which includes labeled nucleic acid residues A spacer segment may optionally also be disposed at either or both of the termini. The labeled nucleic acid monomers of the spacer segments may include labels such as biotin and/or digoxigenin, for secondary detection, e.g., by immunohistochemistry, and/or fluorescently labeled nucleic acid monomers. Detectability is improved for the following reasons. First, the ability to select the sequence of the spacer segments permits these segments to be densely labeled while not affecting the sequence specificity of the complementary first segments. And, second, with particular relevance to indirect detection methods such as immunohistochemistry, when the probe is hybridized to the target sequence, the labeled spacer segments loop out, thereby providing less-hindered access to the labeled monomers of the segment by secondary detection reagents such as avidin and streptavidin (biotin binders) and enzyme conjugates thereof, or anti-digoxigenin antibodies and enzyme conjugates thereof. Such enzyme conjugates may, for example, include those well-recognized in the art such as horseradish peroxidase conjugates and alkaline phosphatase conjugates.
The sequences of at least some of the spacer segments, such as at least half of the spacer segments or all of the spacer segments, may be at least substantially the same, for example, at least 90% or at least 95% or at least 98% identical, or exactly identical to each other. The sequence(s) of the spacer segments may be at least substantially not self complementary.
By consecutive or sequential arrangement of the first segments of a nucleic acid molecule/probe embodiment of the invention what is meant is, in the order the first segments occur in the probe in the 5′ to 3′ direction, these segments hybridize in the same order along the target sequence in its 3′ to 5′ direction. There may be sequence gaps (“gaps”) or no-gaps between the 3′ end of a given first segment of a probe and the '5 end of the next adjacent first segment of the probe (proceeding in the 3′ direction of the probe). The gaps correspond to sequence elements that would be present in a full complementary strand to the target nucleic acid that are not provided by or present between the first nucleic acid segments when they are hybridized to the target. Gaps, if present, may, for example, be in the range of 1-30 residues/nt long with respect to the target strand, or any subrange or numerical value therein such as but not limited to 4-12 residues long. In one variation, a nucleic acid molecule/probe embodiment of the invention has a sequence such that there is a gap between each neighboring first segment when hybridized to the target strand.
The probes of the invention may, for example, be composed of RNA and/or DNA and/or labeled analogs thereof, in any combination thereof. The probes of the invention may be synthesized synthetically, for example, using conventional phosphoramidite chemistry and reagents therefor. The probes of the invention may also be synthesized enzymatically, for example, by template-directed nucleic acid synthesis such but not limited to RNA transcription using common viral promoter systems (e.g., T7 and SP6) for synthesizing RNA probes, and polymerase chain reaction (PCR) for synthesizing DNA probes. For such enzymatic syntheses, labeled nucleotides or ribonucleotides may be included in the reaction mixture for incorporation into the product. For template directed synthesis, it should be understood that the monomer mix will include all complementary monomers to synthesize the complementary strand of the template and may generally include nucleic acid monomers having all four bases (A, G, T/U, C).
In one embodiment, one or more or all of the spacer segments include labeled nucleic acid monomers (labeled residues). Each or all of the target-complementary first segments may include or exclude labeled nucleic acid monomer(s). Where one or more or all of the target-complementary first segments includes labeled nucleic acid monomer(s), the labeled monomers may be the same and/or different than the labeled monomers of the spacer segments. When the probes are chemically synthesized, the type and position of labeled monomers in the probe can be predetermined and precisely controlled, for example, providing labeling only in the spacer segments. When synthesis is polymerase-mediated (template-directed), assuming the same types of bases occur in both the target-complementary first segments and the spacer segments, both will be labeled by incorporation of the labeled nucleic acid monomers.
In related embodiments, the probe may be labeled as above or have the same structure but be unlabeled, and (for either case) secondary nucleic acid molecules that are complementary to the spacer segments of the probe and which themselves are labeled (for direct or indirect detection) are hybridized to said spacer segments to the probe.
Also provided by the invention are compositions of matter that include any of the nucleic acid hybridization probes hybridized to a target nucleic acid sequence of a target polynucleic acid molecule. The target nucleic acid molecule may, for example, be a naturally-occurring nucleic acid molecule or an otherwise biologically expressed nucleic acid molecule (such as the transcript of an artificial transgene). The target nucleic acid molecule may, for example, be a DNA molecule, such as a cellular genomic DNA, such as a chromosome, or viral DNA, or an RNA, such as cellular or viral RNA, such as a cellular or viral mRNA. The composition may, for example, include the probe hybridized to the target sequence in an in situ preparation of tissue or collected cells, such as but not limited to human cervical cells. The in sita preparation may include genomic DNA, for example, include or consist of one or more chromosomes, such as isolated human chromosomes, isolated non-human mammalian chromosomes, or isolated chromosomes of any desired organism and/or viral nucleic acids such as viral DNA or viral RNAs.
The spacer segment sequences may, for example, be uniform in length and/or sequence and/or at least some of the spacer segments may be different in length and/or sequence. The spacer segments may, for example, be from 10-200 monomers long or any subrange or numerical value in said range such as bot not limited to 10-150, 10-100, 20-100, 10-50, 20-50, or 15-30 monomers long. The lengths of the segments of target-complementary sequence (the first nucleic acid segments) may, in at least some instances for a probe, for example, all instances, be in the range of 35-100 monomers long, or any subrange or numerical value therein, such as 50 monomers plus/minus 5 monomers long.
Probes according to the invention specifically hybridize to a target nucleic acid molecule via the first segments of the probe that are complementary to sequences in the target nucleic acid molecule. The spacer segment sequences are selected so that they are at least substantially not complementary to the first segments or to the target nucleic acid molecole. In addition, the spacer segment sequence(s) may be selected so that they, and the overall probe, at least substantially do not hybridize to any non-target polynucleic acid molecules present in a specimen under the same conditions under which the probe specifically hybridizes via the first segments to a target nucleic acid molecule present in the specimen.
The following example demonstrates the preparation of a biotin labeled RNA probe that is useful for in situ detection of HPV16 (human papilloma virus 16) transcripts in mammalian cells, such as isolated, fixed and permeabilized human cervical cells. Probes specifically binding selected transcripts of HPV16 were designed such that extra nucleic acid sequences, i.e., spacer segments with additional label, are interspersed in the target-complementary sequence. SEQ ID NO: 1 (shown in Table 1) is the antisense (binding) strand DNA sequence of an HPV16 E6/E7 gene consensus sequence which served as the basis for preparing probes for detecting the E6 and E7 mRNAs of HPV16. It should be understood that the complementary DNA strand, i.e., the sense strand, is also present throughout preparation of the expression construct and will act as a template for synthesis of anti-sense RNA via transcription.
The SEQ ID NO: 1 DNA was modified by inserting the spacer sequence CACATTGCTCTCTTCCTTTC (SEQ ID NO: 2) after every 50 bases, and at the beginning and end of the sequence, so that RNA transcribed from the template DNA strand will incorporate significant amounts of biotin-labeled cytosine and biotin-labeled uracil ribonucleotide residues in transcribing the spacer segments in addition to those incorporated in transcribing the target (E6/E7 RNA)-complementary sequences: The resulting modified DNA sequence (SEQ ID NO: 3) is shown in Table 2 with the inserted spacer sequences indicated in capital letters. The spacer sequence is internally inserted seventeen times and occurs once at each end.
The SEQ ID NO: 3 modified template DNA was placed after a T7 promoter in a plasmid expression vector for in vitro transcription using T7 RNA polymerase and RNA was transcribed in vitro from the isolated plasmid using the Enzo BIOARRAY HIGHYIELD® RNA transcript labeling kit (T7) (Product No. ENZ-42655; Enzo Life Sciences, Inc., Farmingdale, NY, USA). The transcribed RNA, which includes biotin-labeled cytosine and biotin-labeled uracil ribonucleotide residues, was then hydrolyzed by alkaline hydrolysis to an average size of 200 bases using sodium carbonate/bicarbonate buffer. The resulting biotin labeled RNA fragments were used as a hybridization probe composition to detect nucleic acids in cells in situ using conventional techniques. Similar probes were also made for the HPV16 L1 gene, L2 gene, and E1 gene. E2 gene probes as well as probes for other genes and RNAs may also be made.
In the above example, optional terminal occurrences of the spacer sequence were added. It should be understood that, generally, in addition to internal spacer sequence insertions, a spacer sequence may be added at both termini, at one end only (at the 5′ end of the 3′ end with respect to the antisense sequence), or not at either termini.
In a separate experiment, a mixture of fragmented loop RNA hybridization probes according to the invention that cover substantially all of the HPV-16 genome was prepared and tested. Photomicrographs showing the results with this HPV genome-spanning mixture of probes are shown in
As described, long enzymatically synthesized RNA transcripts may be partially alkaline hydrolyzed to provide a mixture of smaller fragments useful as probes. The mixture may, for example, include fragments in the range of 100-500 residues long, such as 200-400 residues long, such as 250-350 residues long, or any subranges therein. The mixture may, for example, include a substantial fraction of fragments in these size ranges. The mixture of size fragments obtained by the partial alkaline hydrolysis may, if desired, be further size fractionated or enriched, for example, by column chromatography, to obtain a mixture of fragments having a substantial fraction of fragments in the desired size ranges, such as but not limited to the aforementioned size ranges and subranges.
The following protocol may be used to partially alkaline hydrolyze labeled transcribed RNA, such as the biotin-labeled RNA transcripts of the example. 100 μl transcribed RNA (20 μg total) is mixed with 100 μl Hydrolysis Buffer (80 mM NaHCO3, 120 mM Na2CO3, 20 mM β-mercaptoethanol) and heated to 60° C. for 25 minutes. 200 μl Stop Buffer (200 mM sodium acetate, pH 6, 1% Acetic acid, 10 mM dithiothreitol) is then added, after which 40.88 μl 3 M sodium acetate, pH 5.2 and 8.77 μl Yeast tRNA (11.4 mg/ml) are added. Finally, 1124 μl ethanol is added with mixing, and the mixture is stored at −80° C. for 2 hours. The fragmented RNA is then precipitated by centrifugation at 4° C. at 16,000×g for 20 minutes at 4° C. The supernatant is carefully removed, and the pellet is washed with 700 μl ice cold 70% ethanol, and centrifuged again at 16,000×g for 5 minutes at 4° C. The supernatant is again removed, and the tube spun a second time for 15 seconds to bring all the remaining liquid down, which is then removed. The pelleted fragmented RNA is then resuspended in 100 μl of 10 mM TrisHCl, pH 7.0, 1 mM EDTA to form an RNA Hybridization Probe Stock Solution.
Single-stranded DNA probes may also be synthesized enzymatically. For example, a pair of peripheral DNA PCR primers may be used to amplify by PCR a double-stranded DNA molecule, which is SEQ ID NO: 3 hybridized to its complement, in a reaction including digoxigenin-labeled cytosine deoxynucleotides (dCTP) and digoxigenin-labeled uracil deoxynucleotides (dUTP), and/or, for example, fluorescently labeled versions of these same deoxynucleotides One of the PCR primers of the pair, such as the one that extends the sense strand of the amplicon. may be labeled with biotin so that the sense strand can be bound to an avidin or streptavidin support/bead and separated from the anti-sense strand, e.g., using NaOH, while biotin-streptavidin binding remains unperturbed. The isolated, labeled, anti-sense DNA strand can then be used as a single-stranded hybridization probe, for example, for detecting particular mRNAs. The isolated, single-stranded, anti-sense DNA may be used directly as a probe and/or may be fragmented, for example, into a probe composition of fragments, for example, having average length of 180-220 bases. Fragmentation of single-stranded DNA may be performed by any suitable method such as Point-sink Shearing (PtS; Thorstenson et al., An Automated Hydrodynamic Process for Controlled, Unbiased DNA Shearing, Genome Res. 1998 Aug; 8(8): 848-855); acoustical shearing such as Covaris truSHEAR™ Mechanical DNA Shearing (Covaris, Inc., Woburn, MA, USA), needle shearing (by creating shearing forces by passing DNA through a small gauge needle), nebulization-based (using compressed air to force DNA through a small hole in a nebulizer unit, and collecting the fragmented, aerosolized DNA-DNA fragment size is determined by the pressure used), and DNAse I treatment.
Still other enzymatic methods for producing single-stranded DNA hybridization probes according to the invention include asymmetric PCR. (using labeled nucleotides) and rolling circle amplification (using labeled nucleotides). See Marimuthu et al., Single-stranded DNA (ssDNA) production in DNA aptamer generation, Analyst, 2012, 137, 1307 for a review of methods for producing single-stranded DNA that are readily adaptable to production of single-stranded DNA probes according to the invention. The labeled single-stranded DNA molecules according to the invention that may be obtained using these or any methods may, optionally, also be fragmented to obtain probe compositions as described above.
Fragmentation may also be performed by specifically cleaving the spacer segments, for example by sequence specific cleavage, for example, by using a restriction enzyme. There may, for example, be little, no or only predefined concomitant cleavages within the target-complementary segments. In a related embodiment, the spacer segments are selectively cleaved, or are at least substantially selectively cleaved, or are at least predominantly selectively cleaved, versus the target-complementary segments. In a variation, the spacer segments are exclusively cleaved so that the target-complementary segments are not cleaved at all. The invention also provides fragmented nucleic acid hybridization probe compositions that are derived from RNA transcripts or DNA molecules that include target-complementary segments and spacer segments as described herein and which are further processed by specifically and/or selectively cleaving the transcripts/molecules within one or more or all of the spacer segments. In these embodiments, the sequence of the spacer segments may, for example, be selected (predetermined) to include a subsequence (sequence element) that renders the spacer segment a target for a polynucleic acid cleaving enzyme in the presence of any required accessory molecules under reaction conditions for the enzyme. In a related embodiment, the transcript/molecule is cleaved within the spacer sequences, such as at least predominantly within the spacer sequences versus the target-complementary sequences, to obtain a fragmented probe composition.
For example, for a long ssDNA molecule including target-complementary segments and spacer segments as described herein, a segment of the spacer sequence can be the recognition sequence of one strand for a preselected dsDNA restriction enzyme. A synthetic oligonucleotide the same size as or slightly larger than and including complementary sequence to the recognition site is added to and permitted to hybridize to the long dsDNA molecule to constitute a full double stranded restriction enzyme recognition sequence with the subject spacer segments. A restriction enzyme reaction is constituted by adding the restriction enzyme in a suitable buffer and incubating the mixture at a permissive temperature, thereby causing the spacer segments to be cleaved at the restriction sites characteristic of the subject restriction enzyme. The resulting DNA fragments may then be extracted from the reaction by a conventional aqueous: organic extraction or by any clean-up means known in the art. A size exclusion process may optionally be employed to remove any small nucleic acid molecules from the mix, such as remaining oligonucleotides and/or fragments thereof, as known in the art. In general, the selection of a restriction enzyme recognition sequence and corresponding restriction enzyme may be driven by the need or lack thereof to exclude or minimize cutting by the enzyme within the target complementary segments of the long ssDNA molecule. For example, if it desired to have no cleavage whatsoever within any of the target complementary segments, then a restriction enzyme recognition sequence that does not occur at all in the target complementary segments should be used in the spacer segment(s). On the other hand, cuts in one or a few of the target complementary segments may not be detrimental to the performance of the resulting probe composition and, thus, may be tolerable in given situation. The restriction enzyme used for this purpose may, for example, be a rare cutter, i.e., a restriction enzyme having a recognition site 7, 8 or more nucleotide residues in length, such as but not limited to Not1 which cuts after the first GC of sequence 5′-GCGGCCGC-3′. The restriction enzyme may, for example, be Xcml and the method of Shaw and Muck.Xcml as a universal restriction enzyme for single-stranded DNA, Gene 133 (1993) pp. 85-89, may be employed. The restriction enzyme may, for example, be a Class IIS enzyme and the method of Podhajska et al., Conferring new specificities on restriction enzymes: cleavage at any predetermined site by combining adapter oligodeoxynucleotide and Class IIS enzyme, Methods in Enzymology, 1992 Vol. 216, pp. 303-309, may be employed.
In a variation, one or more spacer segments having a self-complementary section that forms a restriction enzyme recognition site when self hybridized is used and is digested using a cognate dsDNA restriction enzyme. In another variation, one or more or all of the spacers include a recognition site sequence for a restriction enzyme having single stranded DNA activity such as AvaII, HaeII, DdeI, AluI, Sau3AI, AceII, TthHB8I and HapII, and said enzyme is used to cleave said one or more or all spacer segments without the need to provide a separate nucleic acid, such as an oligonucleotide, that is complementary to said recognition site. Without being limited to theory, it is believed that these restriction enzymes cleave ssDNA by recognizing and cleaving transiently formed secondary structures (called canonical structures) in ssDNA composed of two recognition sequences with two fold rotational symmetry. See Nishigaki et al., Type II restriction endonucleases cleave single-stranded DNAs in general, Nucleic Acids Res. 1985, Vol, 13 No. 16, 5747-5760.
In a related embodiment in which spacer sequences of a long single stranded DNA are selectively cleaved, rather than a restriction enzyme, crab duplex-specific nuclease (e.g., Catalog No. BA001 Evrogen, Moscow, Russia) is used to preferentially cut DNA of spacer sequences that are hybridized to a provided short RNA oligonucleotide, which may, for example, be synthetic. See also: U.S. Pat. Nos. 7,435,794, 7,803,922; 7,951,569; Anisimova et al., Isolation characterization and molecular cloning of Duplex-Specific Nuclease from the hepatopancreas of the Kamchatka crab, BMC Biochemistry 2008, 9.14; and Shagin, et al., A novel method for SNP detection using a new duplex-specific nuclease from crab hepatopancreas, 2002 Genome Research. 12 (12) pp. 1935-42.
Still another way to selectively cleave particular ssDNA sequences that may be used to implement the present invention involves the use of Argonaute polypeptide: guide molecule complexes as nucleic acid-guided restriction enzymes for DNA substrates as disclosed in U.S. Pub. No. 20160289734 to Zamore et al.
One or more or all of spacer segments (or any desired location) of a non-naturally occurring single stranded RNA molecule according to the invention may be similarly selectively cleaved by incorporating therein a restriction enzyme recognition site of a restriction enzyme, such as AvaII, AvrII, BanI, HaeIII, HinfI and/or TaqI, that recognizes and cleaves RNA in an RNA:DNA duplex that may be formed with said RNA molecule by hybridizing a DNA oligonucleotide, which may be synthetic, to form the hybrid restriction site and constituting a reaction mixture including the subject restriction enzyme(s) under conditions permissive for its activity. See, e.g., Murray et al., Sequence-specific cleavage of RNA by Type II restriction enzymes, Nucleic Acids Research, 2010, Vol 38, No. 22 8257-8268. Engineered RNA endonucleases may also be used, such as those disclosed in Choudhury et al., Engineering RNA endonucleases with customized sequence specificities, Nature Communications 2012 DOI: 10.1038/ncomms2154. Still another way to selectively cleave particular ssRNA sequences that may be used to implement the present invention involves the use of Argonaute polypeptide guide molecule complexes as nucleic acid-guided restriction enzymes for RNA substrates as disclosed in U.S. Pub. No. 20160289734 to Zamore et al.
Various fluorescently labeled and hapten-labeled ribonucleoside triphosphates (rNTPs) and deoxynucleoside triphosphates (dNTPs) are commercially available for polymerase-mediated synthesis of probes according to the invention, such as but not limited to Cyanine 3 UTP enhanced (ENZ-42505, Enzo Life Sciences), Cyanine 5-UTP enhanced (ENZ-42506), Fluorescein-12-UTP (ENZ-42834), Biotin-11-CTP (ENZ-42818), Biotin-16-UTP (ENZ-42814), Digoxigenin-UTP alkali-stable (ENZ-NUC114-0250), Cyanine 3-dUTP (ENZ-42501), Cyanine 5 dUTP (ENZ-42502), and Digoxigenin-dUTP alkali-stable (ENZ-NUC113-0025). Rather than directly enzymatically incorporating fluorescently labeled or hapten-labeled rNTPS or dNTPs into the probes, allyl amine labeled rNTPS or dNTPs (aminoallyl rNTPS or dNTPs), such as but not limited to aminoallyl dUTP (ENZ-42861) and aminoallyl UTP (R1091, ThermoFisher Scientific), may be incorporated and then reacted with fluorescent dye or hapten derivatives to functionally label the probe, as known in the art. The aminoallyl group is reactive with N-hydroxysuccinimide (NHS) ester groups of commercially available label derivatives to form a bond with the primary amino group of the incorporated rNTP analog or dNTP analog. As to chemical synthesis of nucleic acid probes according to the invention, a variety of labeled phosphoramidites are available for incorporation into an oligonucleotide, such as into the loop portions of probes according to the invention, by phosphoramidite chemistry such as but not limited to biotin phosphoramidite (e.g., M042000, Millipore Sigma), Cyanine 3 phosphoramidite (e.g., M047000, Millipore Sigma), Cyanine 5 phosphoramidite (e.g., M046030, Millipore Sigma), fluorescein phosphoramidite (e.g., M041080, Millipore Sigma), 6-fluorescein phosphoramidite (e.g., M041100, Millipore Sigma) and 6-hexachloro-fluorescein phosphoramidite (e.g., M043130, Millipore Sigma).
The invention also provides nucleic acid “spacer segmented” probes labeled as described along with the aforementioned variations thereof, as well as corresponding probe embodiments that are not labeled but which otherwise have the same structure (and optionally any or all of the variations thereof described herein), for hybridization to a target nucleic acid molecule, such as a naturally occurring target nucleic acid molecule, and detection by labeled nucleic acid probes, such as labeled oligonucleotide probes, that are complementary to and hybridize with one or more or all of the spacer segments of the nucleic acid “spacer segmented” probes.
Accordingly, one embodiment of the invention provides a non-naturally occurring linear nucleic acid molecule having a 5′ end and a 3′ end, which includes:
A further embodiment of the invention provides a composition of matter that includes this non-naturally occurring linear nucleic acid molecule and one or more labeled nucleic acid probes, such as labeled oligonucleotide probes, that are complementary to and hybridized with one or more or all of the spacer segments of said non-naturally occurring linear nucleic acid molecule.
Another embodiment of the invention provides a composition of matter that includes this non-naturally occurring linear nucleic acid molecule and a naturally occurring target nucleic acid molecule to which the non-naturally occurring linear nucleic acid molecule is hybridized by way of the first nucleic acid segments.
A still further embodiment of the invention provides a composition of matter that includes:
For embodiments including a labeled non-naturally occurring linear nucleic acid as described and one or more labeled nucleic acid probes hybridized to the spacer segments thereof, the detectable labels of the former and the latter may be entirely the same type, entirely different types, or have at least one detectable label type in common and also have at least one detectable label type not in common.
Unlabeled non-naturally occurring linear nucleic acid molecule embodiments of the invention (and fragmented probe composition embodiments derived therefrom) may be prepared using the same method embodiments disclosed herein for labeled embodiments by leaving out the labeled nucleic acid monomers, i.e., by using only unlabeled nucleic acid monomers. Such unlabeled non-naturally occurring linear nucleic acid molecule embodiments of the invention may also be fragmented as described herein to provide a fragmented probe composition (optionally with any or all of the same variations and further processing of fragmented compositions described herein with respect to labeled embodiments).
A still further embodiment of the invention provides a method for detecting a target nucleic acid sequence in a sample that includes the steps of:
Any and all publications, patents, patent applications and other documents cited in this application are hereby incorporated by reference in their entireties for all purposes to the same extent as if each individual publication, patent, patent application or other document were individually indicated to be incorporated by reference for all purposes.
While various specific embodiments have been illustrated and described, it will be appreciated that various changes can be made without departing from the spirit and scope of the invention(s). Moreover, features described in connection with one embodiment of the invention may be used in conjunction with other embodiments, even if not explicitly exemplified in combination within.
This application is a continuation-in-part of International application no. PCT/US2019/029036 filed Apr. 25, 2019, which claims priority to U.S. application Ser. No. 16/053,138 filed Aug. 2, 2018 (now U.S. Pat. No. 10,323,272), which claims the benefit of U.S. provisional application Ser. No. 62/624,249 filed Jan. 31, 2018, each of which is hereby incorporated by reference in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| 62624249 | Jan 2018 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 16920773 | Jul 2020 | US |
| Child | 19038602 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/US2019/029036 | Apr 2019 | WO |
| Child | 16920773 | US | |
| Parent | 16053138 | Aug 2018 | US |
| Child | PCT/US2019/029036 | US |
