Patent Application
20240166698
The present disclosure relates to fast, efficient chemical reactions for conjugating proteins, such as the pore-forming protein, α-hemolysin, to biomolecules, such as antibodies, receptors, and enzymes, such as DNA polymerase.
Single-molecule sequencing-by-synthesis (SBS) techniques using nanopores have been developed. See e.g., US Pat. Publ. Nos. 2013/0244340 A1 and 2013/0264207 A1. Nanopore SBS involves the use of a polymerase synthesize a DNA strand complementary to a target sequence template and determine the identity of each nucleotide monomer as it is added to the growing strand, thereby determining the target sequence. Each added nucleotide monomer is detected via a nanopore located adjacent to the polymerase active site and the growing strand. Obtaining an accurate signal requires proper positioning of a polymerase active site near a nanopore. Proper positioning typically is achieved by covalently linking the polymerase to the pore-protein that makes up the nanopore.
Monomeric pore-forming proteins have molecular weights range from as little as 5 kDa to 80 kDa, and these monomers form large multimeric complexes of 6, 7, 8, 9, 10, or more monomers, having molecular weights of 160, kDa, 180 kDa, 200 kDa, 220 kDa, or more. Under suitable conditions these multimeric complexes spontaneously form pores through lipid bilayer membranes. The well-studied pore-forming protein from S. aureus, α-hemolysin (α-HL) has a monomer molecular weight of 33 kDa and spontaneously forms a heptameric pore complex having a molecular weight of 231 kDa. Polymerases are large proteins that range in molecular weight from about 60 kDa to 100 kDa and even much larger multimeric complexes in some cases (e.g., RNA polymerase ˜400 kDa multimer). The Klenow fragment of DNA polymerase I has a molecular weight of 68 kDa.
Accordingly, the kinetics of any reaction to conjugate these pore-forming proteins, like the α-hemolysin heptamer, to large biomolecules, like DNA polymerase, in order to provide a nanopore sensor will be extremely limited by the low concentration achievable (and relative low amounts available) with such large macromolecules. The maximum solubility of such large proteins in aqueous solution typically is limited to approximately 0.1 to 10 mg/mL. Thus, the concentration of the two macromolecules in solution used for a conjugation reaction is limited to ˜1 μM to 1000 μM. For example, the α-hemolysin protein pore consists of 7 identical subunits totaling about 235,000 molecular weight. Thus a solution of 10 mg/ml has a concentration of about 42 μM. This relatively low concentration range effectively limits viable conjugation chemistries to those having extremely fast, irreversible reaction rates.
WO2015/148402A1 describes tagged nucleotides useful for nanopore sequencing, and describes two methods for attaching α-hemolysin to a polymerase. One method involves using the SpyTag-SpyCatcher enzymatic conjugation reaction (see e.g., Zakeri and Howarth (2010).JACS 132:4526-7). In this method, a SpyTag peptide fragment is attached as a recombinant fusion to the C-terminus of an α-HL monomer, and a SpyCatcher protein fragment is attached as a recombinant fusion to the N-terminus of the Phi29 DNA polymerase. A second method involves using an inverse electron demand Diels-Alder (IEDDA) reaction between an α-HL modified with a trans-cyclooctene group and a polymerase modified with a 6-methyl-tetrazine group.
Native Chemical Ligation (NCL) originally was developed as a synthesis method that allowed extension of synthetic polypeptides by ligating polypeptide fragments while maintaining native peptide bonding structure. (see e.g., Dawson et al., “Synthesis of proteins by native chemical ligation,” Science 1994, 266, 776-779) The stoichiometric efficiency and site-specificity of NCL make it useful for glycopeptide synthesis and other synthetic methods where it is important to retain native peptide bonding. (See e.g., Shin et al., “Fmoc-Based Synthesis of Peptide-α-Thioesters: Application to the Total Chemical Synthesis of a Glycoprotein by Native Chemical Ligation,” J. Am. Chem. Soc. 1999, 121, 11684-11689.)
Due to the relatively low-concentrations of pore-protein and polymerase typically used in forming a nanopore detection system for SBS, it is critical that highly efficient and site-specific conjugation reactions are developed that allow strong, selective, covalent conjugation between these two relatively large protein complexes. It is also critical that the conjugation reactions allow for freedom in attachment site selection in order to optimize the positioning of the conjugated molecules for specific uses, such as nanopore sequencing, that require precise macromolecular orientation. Thus, there remains a need for faster and more efficient processes to conjugate protein complexes, such as nanopores, to other biomolecules, such as enzymes.
The present disclosure provides methods for site-specific conjugation of a pore-forming protein and a biomolecule, and the compositions comprising modified pore-forming proteins, biomolecules, and conjugates arising from the use of the methods of preparation. Further, the disclosure provides nanopore systems and compositions comprising the conjugates, and associated uses, including use in nanopore sequencing.
The method for site-selective conjugation of a protein to a biomolecule as disclosed herein generally comprises steps (a)-(c) as follows:
A-LA-X (I)
Y-LA-B (III)
In some embodiments, the present disclosure also provides a composition comprising a modified pore-forming protein of structural formula (IVa)
In some embodiments, the present disclosure also provides a composition comprising a protein-biomolecule conjugate of formula (V)
In embodiments of the site-selective conjugation methods and associated compositions disclosed herein, the reactive group B comprises a SpyTag peptide and the reactive group Z comprises a SpyCatcher protein. In some embodiments, wherein the SpyTag peptide comprises an amino acid sequence selected from AHIVMVDAYKPTK (SEQ ID NO: 1), AHIVMVDAYK (SEQ ID NO: 2), AHIVMVDA (SEQ ID NO: 3), and ahA-AHIVMVDAYKPTK (SEQ ID NO: 4). In some embodiments, the biomolecule comprising a reactive group Z is a fusion with a SpyCatcher protein, optionally wherein the SpyCatcher protein comprises an amino acid sequence of SEQ ID NO: 6, 7, or 8.
In some embodiments, the present disclosure further provides a nanopore composition comprising a protein-biomolecule conjugate of formula (V), wherein the protein is a pore-forming protein that is part of a nanopore. In some embodiments, the nanopore is embedded in a membrane, and optionally, the membrane can be attached to a solid substrate, and/or is formed such that it spans a well or depression or hole in a solid substrate, which optionally comprises a material selected from the group consisting of polymer, glass, silicon, and a combination thereof. In some embodiments, the solid substrate further comprises adjacent to the nanopore a sensor, a sensing circuit, or an electrode coupled to a sensing circuit, optionally, a complementary metal-oxide semiconductor (CMOS), or field effect transistor (FET) circuit.
The disclosure also provides compounds and compositions that form as intermediates in the methods for site-selective conjugation of proteins to biomolecules, including the intermediate composition comprising a modified pore-forming protein of structural formula (IVa).
In embodiments of the site-selective conjugation methods and associated compositions disclosed herein, the protein is a pore-forming protein selected from the group consisting of α-hemolysin, β-hemolysin, γ-hemolysin, aerolysin, cytolysin, leukocidin, melittin, MspA porin, and porin A. In one embodiment, the pore-forming protein is α-hemolysin from Staphylococcus aureus. In one embodiment, the pore-forming protein is α-hemolysin C46 (“α-HL C46”), which comprises α-hemolysin from S. aureus with a K46C amino acid residue substitution. In some embodiments, the pore-forming protein is capable of forming a nanopore of diameter of about 0.5 nanometer to about 25 nanometers.
In some embodiments of the methods of preparation of the conjugate compositions of formula (I), the protein and/or the biomolecule are present in the reaction solution at a concentration of less than 1000 μM, 750 μM, 500 μM, 250 μM, 100 μM, 50 μM, 10 μM, 5 μM, or 1 μM or less.
In embodiments of the site-selective conjugation methods and associated compositions disclosed herein, the protein is a pore-forming protein having a molecular weight of at least 20 kDa, 30 kDa, 40 kDa, 50 kDa, or greater. In some embodiments of the methods and compositions, the biomolecule has a molecular weight of at least 30 kDa, 40 kDa, 50 kDa, 60 kDa, 70 kDa, 80 kDa, or greater. In some embodiments, the pore-forming protein has a molecular weight of at least 30 kDa and the biomolecule has a molecular weight of at least 50 kDa.
In embodiments of the site-selective conjugation methods and associated compositions disclosed herein, the protein is a pore-forming protein that is a part of a multimeric complex, wherein the multimer is selected from hexamer, heptamer, octamer, nonamer, decamer, or larger multimer. In some embodiments, the protein is a pore-forming protein that is a single monomer which is part of a multmeric complex, wherein the other monomers of the complex do not comprise a conjugate composition of formula (V) (i.e., only a single monomer of the multimer is conjugated to the biomolecule).
In embodiments of the site-selective conjugation methods and associated compositions disclosed herein, the protein is pore-forming protein that is embedded in a membrane. In some embodiments, the protein is a pore-forming protein that is part of a nanopore. In some embodiments, the protein is attached to a solid substrate, and optionally the solid substrate comprises a material selected from the group consisting of polymer, glass, silicon, and a combination thereof.
In embodiments of the site-selective conjugation methods and associated compositions disclosed herein, the biomolecule is an enzyme capable of catalyzing the synthesis of a polymer. In some embodiments, the biomolecule is an enzyme selected from the group consisting of a DNA polymerase, RNA polymerase, reverse transcriptase, and DNA ligase. In some embodiments, the biomolecule is a naturally-occurring or non-naturally occurring (e.g., engineered) enzyme that has 5′→3′ DNA polymerase activity and strong strand displacement activity but lacks 5′→3′ exonuclease activity. In some embodiments, the biomolecule is a DNA polymerase, optionally selected from the group consisting of 9° N polymerase, E. coli DNA Polymerase I, E. coli DNA Polymerase II, Bacteriophage T4 DNA polymerase, Sequenase, Taq DNA polymerase, 9° N polymerase (exo-) A485L/Y409V, DNA polymerase Bst 2.0, and Phi29 DNA polymerase (ϕ29 DNA Polymerase). In some embodiments the biomolecule is DNA polymerase Pol6 comprising the amino acid of SEQ ID NO: 9. In some embodiments, the biomolecule comprising a reactive group Z is a fusion of a DNA polymerase Pol6 and a SpyCatcher protein, optionally the fusion comprising the amino acid sequence of SEQ ID NO: 10.
In some embodiments of the compositions and methods of preparation comprising a compound of formula (I), the linkers LA and LB comprise a covalently bonded chain of 2 to 100 atoms comprising one or more of the following chemical groups: linear (C1-C5) alkyl, linear (C1-C5) alkenyl, linear (C1-C5) alkynyl, ester, ether, amine, amide, imide, phosphodiester, and/or polyethylene glycol (PEG). In some embodiments, the linkers LA and LB attach to A and B either through a thioether bond to a sulfhydryl group on A and/or B, or through a peptide bond to a primary amine group of A and/or B. In some embodiments, the linkers LA and LB comprise a polymer of from 1 to 50 polyethylene glycol (PEG) moieties. In some embodiments of the compositions and methods of preparation comprising a compound of formula (I), the linkers LA and LB are independently selected from the group consisting of structures of formula (VIa)-formula (VIe).
The present disclosure is directed to methods for site-selective conjugation of proteins (e.g., the pore-forming protein, α-hemolysin) to other biomolecules (e.g., DNA polymerase oligonucleotides, antibodies and receptors) and the resulting protein-biomolecule conjugates of formula (V)
wherein, S is a sulfur atom of a thiol group of the protein; A is a thiol reactive group; LA is a linker; X is a click chemistry reactive group; Y is a click chemistry reactive group that undergoes a click chemistry reaction with the reactive group X; LB is a linker; B is a reactive group; and Z is a reactive group capable of forming a covalent bond with the reactive group B.
The present disclosure also provides compounds and compositions that form as intermediates in the methods for site-selective conjugation of proteins to biomolecules, including the intermediate composition comprising a modified pore-forming protein of structural formula (IVa)
wherein, S is a sulfur atom of a thiol group of the pore forming protein; A is a thiol reactive group; LA is a linker; and X is a click chemistry reactive group; Y is a click chemistry reactive group that undergoes a click chemistry reaction with the reactive group X; LB is a linker; and B is a reactive group.
The method for site-selective conjugation of a protein to a biomolecule as disclosed herein generally comprises steps of:
A-LA-X (I)
Y-LA-B (III)
The disclosed methods, and compositions allow for fast, efficient conjugation between proteins and other biomolecules at relatively low concentrations and without large mole excesses of one reagent over the other. Accordingly, the compositions and chemical processes for preparing the conjugates disclosed herein are particularly well-suited for use in preparing nanopore compositions comprising a pore-forming protein embedded in a membrane covalently linked to a biomolecule, such as a DNA polymerase. Such nanopore compositions can be used in applications requiring nanopore detection, including single-molecule DNA sequencing-by-synthesis.
Further details of the compositions, methods, and parameters for use in the methods of site-selective conjugation of proteins to biomolecules are described herein below.
For the descriptions herein and the appended claims, the singular forms “a”, and “an” include plural referents unless the context clearly indicates otherwise. Thus, for example, reference to “a protein” includes more than one protein, and reference to “a compound” refers to more than one compound. The use of “comprise,” “comprises,” “comprising” “include,” “includes,” and “including” are interchangeable and not intended to be limiting. It is to be further understood that where descriptions of various embodiments use the term “comprising,” those skilled in the art would understand that in some specific instances, an embodiment can be alternatively described using language “consisting essentially of” or “consisting of.”
Where a range of values is provided, unless the context clearly dictates otherwise, it is understood that each intervening integer of the value, and each tenth of each intervening integer of the value, unless the context clearly dictates otherwise, between the upper and lower limit of that range, and any other stated or intervening value in that stated range, is encompassed within the invention. The upper and lower limits of these smaller ranges may independently be included in the smaller ranges, and are also encompassed within the invention, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding (i) either or (ii) both of those included limits are also included in the invention. For example “1 to 50” includes “2 to 25”, “5 to 20”, “25 to 50”, “1 to 10”, etc.
It is to be understood that both the foregoing general description, including the drawings, and the following detailed description are exemplary and explanatory only and are not restrictive of this disclosure.
The technical and scientific terms used in the descriptions herein will have the meanings commonly understood by one of ordinary skill in the art, unless specifically defined otherwise. Accordingly, the following terms are intended to have the following meanings.
The site-selective conjugation methods disclosed herein for the preparation of a conjugate between a protein, such as the pore-forming protein, α-hemolysin, and a biomolecule, such as DNA polymerase, generally require reagents comprising linkers and reactive groups (or reactive moieties) that react with groups on either the protein or the biomolecule. This conjugation method generally comprises the following steps (a), (b), and (c):
A-LA-X (I)
Y-LA-B (III)
As shown above, the general method requires reagent compounds of formula (I) and (III) and results in two modified protein intermediates of formulas (II) and (IV). The protein-biomolecule conjugates of formula (V), thus results from three covalent bond forming reactions at each of steps (a), (b) and (c).
Step (a) comprises the covalent modification of a thiol group on the protein with a linker comprising a click chemistry reactive group of formula (I) resulting in a modified protein of formula (II). This step essentially modifies the protein such that it is capable of further modification via a facile and efficient click-chemistry reaction.
In some embodiments, the protein has one reactive thiol group such that the modified protein of formula (II) is modified at a single amino acid residue position. For example, the reactive thiol group can be the thiol group of a cysteine amino acid residue located on the surface of the protein or any other region exposed to solvent such that it can react with thiol reactive group A of the compound of formula (I). In some embodiments, the protein is a variant that has been engineered via recombinant DNA techniques so as to have only a single cysteine residue available for modification by the compound of formula (I).
In one embodiment, the protein is the pore-forming protein α-hemolysin from Staphyloccocus aureus (also referred to herein as “α-HL”). α-HL is one of the most-studied members of the class of pore-forming proteins, and has been sequenced, cloned, extensively characterized structurally and functionally using a wide range of techniques including site-directed mutagenesis and chemical labelling (see e.g., Valeva et al. (2001), and references cited therein). In particular, α-HL has had cysteine residue substitutions inserted at numerous positions allowing for covalent modification of the protein through maleimide linker chemistry (Ibid.) In some embodiments, the α-hemolysin useful in the methods of the present disclosure can be a non-naturally occurring engineered pore-forming protein α-hemolysin-C46 (“α-HL-C46”), which comprises α-hemolysin from S. aureus with a K46C amino acid residue substitution.
As shown by the structural depiction above, the compound of formula (I) generally comprises: a thiol reactive group, A, a linker, LA, and a click chemistry reactive group, X. Generally, the compound of formula (I) should react efficiently and selectively under relatively mild aqueous conditions to form a covalent linkage between a thiol group on the protein and the click-chemistry reactive group, X. Further, the click chemistry reactive group, X, should not react with the protein under the conditions wherein the thiol reactive group A reacts with the thiol group of the protein, because X must be available to undergo a reaction with its cognate click chemistry reactive group, Y at step (b).
As noted above, the click chemistry reactive group, X must be selected so as to pair with its cognate click chemistry reactive group, Y used in step (b). Click chemistry reactive groups X and Y useful in the method can be selected from the following pairs of click chemistry reactive groups: azide and alkyne; azide and cyclooctyne; and azide and dibenzocyclooctyne-amine. Accordingly, in some embodiments of the compound of formula (I), the click chemistry reactive group, X is selected from alkyne, cyclooctyne, and dibenzocyclooctyne-amine. Alternatively, in some embodiments, the compound of formula (I), the click chemistry reactive group, X is an azide group.
Many thiol reactive groups that react selectively under mild conditions with protein cysteine groups are known in the art. Thiol reactive groups, A, known to be compatible with the above click-chemistry reactive group pairs and thus, particularly useful in the methods of the present disclosure as thiol reactive group A, are a maleimide group and a haloacetamide group. Accordingly, in some embodiments of the compound of formula (I), the thiol reactive group A is selected from a maleimide and a haloacetamide.
Generally, the linker, LA should provide a covalent tether while also providing adequate spacing between the protein and the click chemistry reactive group X, and ultimately the biomolecule that is conjugated via the method. Because the method of steps (a)-(c) comprises a second linker, LB in the compound of formula (III) used in step (b), the spacing provided by the combination of the two linkers, LA and LB that are part of the conjugate of formula (V), can also be considered.
Accordingly, in general embodiments of the present disclosure, the linker groups, LA and LB useful in the compounds of formula (I) and (III) for carrying out the site-selective conjugation method comprising steps (a)-(c) can include a covalently bonded chain of 2 to 100 atoms comprising one or more of the following chemical groups: linear (C1-C5) alkyl, linear (C1-C5) alkene, linear (C1-C5) alkyne, ester, ether, amine, amide, imide, phosphodiester, and/or polyethylene glycol (PEG). PEG linkers are well-known for use in conjugating biomolecules. Accordingly, in certain embodiments of the compositions of the present disclosure, the linkers LA and LB comprise a polymer of from 1 to 50 PEG moieties, in some embodiments, a polymer of from 2 to 25 PEG moieties, and in some embodiments, a polymer of from 2 to 15 PEG moieties. In some embodiments the linkers, LA and LB have different lengths and/or structures. It is also contemplated that in some embodiments LA and LB are the same.
Specific linker groups useful in the methods of the present disclosure are well-known and commercially available for use in conjugating or cross-linking proteins or other biomolecules. (See e.g., catalog of “crosslinking reagents” available from Thermo Scientific, USA at www.piercenet.com or Sigma-Aldrich, USA at www.sigmaaldrich.com).
Specific embodiments of the compounds of formula (I) are provided in greater detail below.
In some embodiments, the compound of formula (I) comprises a compound of formula (Ia) or (Ib) as shown in Table 1.
In some embodiments, the compound of formula (I) comprises a compound selected from compounds of formula (Ic), (Id), (Ie), (If), (Ig), and (Ih) as shown in Table 2.
In some embodiments, the compound of formula (I) comprises a compound selected from compounds of formula (Ii), and (Ij) as shown in Table 3.
In some embodiments, the compound of formula (I) comprises a compound selected from compounds of formula (Ik), and (Im) as shown in Table 4.
Step (b) comprises the click chemistry reaction the group X on the modified protein of formula (II), and the cognate click chemistry group Y on the reagent compound of formula (III). This step results in the intermediate modified protein compositions of formula (IV) and (IVa) (see above). It is the reactive group B on this intermediate compound of formula (IV) that undergoes the final site-selective reaction with the biomolecule in step (c).
As shown by the structural depiction above, the compound of formula (III) used as a reagent in step (b) generally comprises: a click chemistry reactive group, Y, a linker, LB, and a reactive group, B. The click chemistry reactive group, Y must be selected so as to pair with its cognate click chemistry reactive group, X used in step (a). As noted above, click chemistry reactive groups X and Y useful in the method can be selected from the following pairs of click chemistry reactive groups: azide and alkyne; azide and cyclooctyne; and azide and dibenzocyclooctyne-amine. In some embodiments of the compound of formula (III), the click chemistry reactive group, Y is an azide group. An azide group will undergo a click chemistry reaction with cognate X groups selected from alkyne, cyclooctyne, and dibenzocyclooctyne-amine. Alternatively, in some embodiments, the compound of formula (III), the click chemistry reactive group, Y is selected from alkyne, cyclooctyne, and dibenzocyclooctyne-amine.
The cognate click chemistry reactive group Y of the reagent compound of formula (III) will react efficiently and selectively under relatively mild conditions to form a covalent linkage with the click-chemistry reactive group, X of the modified protein of formula (II). The resulting further modified protein of formula (IV) comprises a covalent linkage, depicted schematically herein (see compound of formula (IV) above) as a single line between X and Y, however, this linkage comprises heterocyclic (e.g., triazole) chemical moiety with a structure dependent on the two click chemistry reactive groups X and Y.
Generally, the linker, LB should provide a covalent tether while also providing adequate spacing between the protein and the click chemistry reactive group Y, and ultimately the biomolecule that is conjugated via the method. As noted above, because the method of steps (a)-(c) comprises two linkers, LA and LB, the spacing provided by the combination of the two linkers in combination can be considered in selecting linker, LB in the compound of formula (III).
Accordingly, in some embodiments the linker group, LB useful in the compound of formula (III) can include a covalently bonded chain of 2 to 100 atoms comprising one or more of the following chemical groups: linear (C1-C5) alkyl, linear (C1-C5) alkene, linear (C1-C5) alkyne, ester, ether, amine, amide, imide, phosphodiester, and/or polyethylene glycol (PEG).
The selection of the linker LB can also depend on the reactive group B selected for the compound of formula (III). As discussed in greater detail below, a shorter linker LB (e.g., 2-3 carbons) can be used where the reactive group B is a SpyTag peptide, which comprises a chain of 13 amino acids, or a longer linker LB (e.g., 5-50 carbons) can be selected when the reactive group B is a benzyl thioester group.
Various embodiments of the modified protein of formula (IV), where the protein is a pore-forming protein as in (IVa), and that illustrate the various heterocyclic covalent linkage structures that can form upon click reaction of the reactive group Y and the reactive group X are shown below in Table 5 as compounds of formulas (IVb)-(IVi).
Generally, the selection of the reactive group B of the compound of formula (III) will depend on the reactive group Z which is the target group of the biomolecule for site-selective conjugation in the reaction of step (c).
In one embodiment, the reactive group Z of the biomolecule comprises an N-terminal cysteine residue and the reactive group B selected is a thioester. The thioester reactive group B can undergo a “Native Chemical Ligation” reaction (also referred to herein as “NCL reaction”) that forms a covalent linkage comprising a peptide bond. (See e.g., Dawson et al., “Synthesis of proteins by native chemical ligation,” Science 1994, 266, 776-779.) Embodiments of the compounds of formula (III) useful wherein the reactive group Z of the biomolecule comprises an N-terminal cysteine residue and a NCL reaction is used for conjugation are provided in greater detail below.
In some embodiments, where the reactive group Z comprises an N-terminal cysteine residue, the compound of formula (III) can comprise a compound of formula (IIIa) or (IIIb) as shown in Table 6.
In specific embodiments wherein the reactive group Z of the biomolecule comprises an N-terminal cysteine residue, the reactive group B is a benzyl thioester.
In further specific embodiments where the reactive group Z comprises an N-terminal cysteine residue, the compound of formula (III) can comprise a compound of formula (IIIc) or (IIId) as shown in Table 7.
In another embodiment, the reactive group Z of the biomolecule comprises a SpyCatcher protein and the reactive group B selected is a SpyTag peptide. The SpyCatcher protein and SpyTag peptide undergo a reaction between a lysine residue of the protein and an aspartic acid residue of the peptide that results in a covalent linkage conjugating the two. (See e.g., Zakeri and Howarth (2010).JACS 132:4526-7; and Li et al., J.Mol.Biol. 2014 January 23; 426(2): 309-317.) Embodiments of the compounds of formula (III) useful wherein the reactive group Z of the biomolecule comprises a SpyCatcher protein and the SpyCatcher-SpyTag reaction is used for conjugation are provided in greater detail below.
Generally, in the methods of the present disclosure when the reactive group Z comprises a SpyCatcher protein, the reactive group B of the compound of formula (III) should comprise a SpyTag peptide. Accordingly, in specific embodiments, the compound of formula (III) can comprise a compound of formula (IIIe) or (IIIf) as shown in Table 8.
Further, since the modified protein of formula (IV) is the result of step (b), it is contemplated that in some embodiments, the reactive group B of formula (IV) comprises a SpyTag peptide. Accordingly, in specific embodiments, the modified protein compound of formula (IV) can comprise a compound of formula (IVi) or (Vk) as shown in Table 9.
As described elsewhere herein, the SpyTag peptide and SpyCatcher protein each comprise a fragment of an amino acid sequence of the CnaB2 domain from the Streptococcus pyogenes fibronectin binding protein FbaB. (See e.g., Li et al., J.Mol.Biol. 2014 January 23; 426(2): 309-317). Generally, the SpyTag peptide comprises a reactive aspartic acid residue from a smaller C-terminal fragment (e.g., 8-20 amino acids), and the SpyCatcher protein comprises a reactive lysine residue from a larger N-terminal fragment (e.g., 100-140 amino acids). The reactive aspartic acid residue of the SpyTag peptide naturally binds to the SpyCatcher protein in an optimal conformation such that the aspartic acid reacts with the lysine to forms a covalent linkage between the two.
Exemplary C-terminal CnaB2 domain sequence fragments useful as SpyTag peptide in the methods and compositions of the present disclosure comprise the following 13 aa amino acid sequence from Li et al., J.Mol.Biol. 2014 January 23; 426(2): 309-317: AHIVMVDAYKPTK (SEQ ID NO: 1). Other CnaB2 C-terminal sequence fragments useful as SpyTag peptides in the methods and compositions of the present disclosure can include shorter fragments of the SpyTag peptide of SEQ ID NO: 1, such as AHIVMVDAYK (SEQ ID NO: 2), and AHIVMVDA (SEQ ID NO: 3).
In some embodiments, it is contemplated that SpyTag peptides useful in the methods and compositions of the present disclosure can comprise additional amino acids, such as modified amino acids, which allow the SpyTag to be covalently attached to linkers. In some embodiments, the SpyTag can comprise an azido-modified amino acid at its N-terminus, such as 4-azido-L-homoalanine (“L-ahA”). Accordingly, an exemplary SpyTag peptide can comprise the following amino acid sequence: (L-ahA)AHIVMVDAYKPTK (SEQ ID NO:4). A range of azido-, alkyne- and other group modified amino acids useful for click chemistry and other facile, high-efficiency covalent attachment chemistries are known in the art and commercially available.
The SpyCatcher protein can comprise a range of amino acid sequences that comprise an N-terminal fragment of the CnaB2 domain of the Streptococcus pycogenes fibronectin binding protein, FbaB that includes Lys31 but excludes Asp117.
In some embodiments, a SpyCatcher protein useful in the methods of the disclosure can include the 138 aa amino acid sequence of SEQ ID NO: 2.
A CnaB2 domain of the Streptococcus pycogenes fibronectin binding protein, FbaB, useful as a SpyCatcher protein in the methods of the present disclosure can include the following 144 aa sequence from Li et al., J.Mol.Biol. 2014 January 23; 426(2): 309-317:
An exemplary N-terminal CnaB2 domain sequence fragment useful as SpyCatcher protein in the methods of the present disclosure includes the following 129 aa amino acid sequence:
DYDIPTTENLYFQGAMVDTLSGLSSEQGQSGDMTIEEDSATHIKFSKRDEDGKELAGATMELRDS SGKTISTWISDGQVKDFYLYPGKYTFVETAAPDGYEVATAITFTVNEQGQVTVNGKATKGDAHI (SEQ ID NO: 6). In some embodiments, the N-terminal CnaB2 domain sequence fragment useful as SpyCatcher protein in the methods of the present disclosure includes the following 138 aa amino acid sequence from Li et al., J.Mol.Biol. 2014 January 23; 426(2): 309-317:
It is contemplated that SpyCatcher proteins useful in the methods and conjugate compositions of the present disclosure can comprise additional amino acid linkers at the N- and C-terminii to facilitate purification and fusion to a biomolecule (e.g., DNA polymerase). An exemplary SpyCatcher protein comprising additional amino acid sequences (e.g., N-terminal His tag and C-terminal GGS linker) has the following 143 aa sequence:
In some embodiments of methods and compositions of the present disclosure, it is contemplated that a fusion of a SpyCatcher protein and a biomolecule can be used. In some embodiments, the fusion comprises a SpyCatcher protein sequence attached via its C-terminus to the N-terminus of the biomolecule aa sequence, wherein the fusion optionally comprises a polypeptide linker sequence between the SpyCatcher protein and the biomolecule.
Similarly, the SpyTag peptide can comprise a range of amino acid sequences that comprise a C-terminal fragment of the CnaB2 domain of the Streptococcus pycogenes fibronectin binding protein, FbaB that includes Asp117 but excludes Lys31. In some embodiments, a SpyTag peptide useful in the methods and compositions of the present disclosure can include an amino acid sequence selected from SEQ ID NO: 1, 2, 3, and 4. In one embodiment, the SpyTag peptide comprises the amino acid sequence of SEQ ID NO: 1.
Step (c) comprises the final covalent linkage forming reaction between reactive group B of the modified protein of structural formula (IV) and reactive group Z of the biomolecule. This reaction results in the formation of the protein-biomolecule conjugate composition of formula (V). As described above, the selection of the reactive groups B and Z will dictate suitable reaction conditions for step (c). Both the NCL reaction conditions and the SpyTag-SpyCatcher reaction conditions are well-known in the art and useful in the step (c) reaction of the present disclosure. (See e.g., Dawson et al., (1994) Science 266, 776-779; Zakeri and Howarth (2010) JACS 132:4526-7; and Li et al. (2014) J.Mol.Biol. 23; 426(2): 309-317.)
Various embodiments of the protein-biomolecule conjugate composition of formula (V) that is the product of step (c) reaction are shown below in Table 10 as compounds of formulas (Vb)-(Vm).
The disclosed site-selective conjugation methods comprising steps (a)-(c) allow for fast, efficient conjugation between proteins and other biomolecules at relatively low concentrations and without large mole excesses of one reagent over the other. Accordingly, the compositions and chemical processes for preparing the conjugates disclosed herein are particularly well-suited for use in preparing nanopore compositions comprising a pore-forming protein embedded in a membrane covalently linked to a biomolecule, such as a DNA polymerase. Such nanopore compositions can be used in applications requiring nanopore detection, including single-molecule DNA sequencing-by-synthesis.
The general site-selective conjugation methods comprising steps (a)-(c) disclosed herein can be used with a wide range of pore-forming proteins, in both naturally-occurring, and non-naturally occurring (e.g., engineered or recombinant) forms of the protein. A wide range of pore-forming proteins are known in the art, and the conjugation reagents and methods provided herein should be broadly applicable to them due to their common amino acid polymeric structure. Accordingly, in some embodiments of the present disclosure, the pore-forming protein used in the methods comprising steps (a)-(c) are selected from the group consisting of α-hemolysin, β-hemolysin, γ-hemolysin, aerolysin, cytolysin, leukocidin, melittin, MspA porin and porin A.
It is a surprising advantage of the site-selective conjugation methods comprising steps (a)-(c) disclosed herein that the conjugate compositions of formula (V) are formed fast and efficiently even though both the pore-forming protein and the biomolecule are large proteins, and accordingly only available in the reaction solution in relatively low concentrations. For example, in some embodiments of the methods of preparation of the conjugate compositions of formula (I), the protein and/or the biomolecule are present in the reaction solution at a concentration of less than 1000 μM, 750 μM, 500 μM, 250 μM, 100 μM, 50 μM, 10 μM, 5 μM, or 1μM or less.
Because the quick and efficient site-selective conjugation methods comprising steps (a)-(c) allow for such low reactant concentrations, the compositions and methods of preparation proteins and biomolecules in much higher weight ranges. Thus, in some embodiments of the compositions and methods of preparation disclosed herein, the protein has a molecular weight of at least 20 kDa, 30 kDa, 40 kDa, 50 kDa, or greater. In some embodiment of the composition, the biomolecule has a molecular weight of at least 30 kDa, 40 kDa, 50 kDa, 60 kDa, 70 kDa, 80 kDa, or greater. In some embodiments, the protein has a molecular weight of at least 30 kDa and the biomolecule has a molecular weight of at least 50 kDa.
Moreover, the site-selective conjugation method comprising steps (a)-(c) has the surprising advantage of allowing for the formation of conjugates of formula (II), (IV), and (V) wherein the protein is part of a large multimeric protein complex. Accordingly, in some embodiments of the compositions and methods of preparation disclosed herein, the protein is pore-forming protein that is a part of a multimeric complex, wherein the multimer is selected from hexamer, heptamer, octamer, nonamer, decamer, or larger multimer. In some embodiments, the pore-forming protein is a single monomer which is part of a multmeric complex, wherein the other monomers of the complex are not modified in the method of steps (a)-(c) (i.e., only a single monomer of the multimer is conjugated to the biomolecule).
Generally, the pore-forming proteins useful in the embodiments of the present disclosure are capable of spontaneously self-assembling nanopores in membranes, wherein the nanopore has a diameter in a range from about 0.5 nanometer to about 25 nanometers. In some embodiments of the compositions and methods disclosed herein, the protein is a pore-forming protein that is embedded in a membrane, and thereby forming a nanopore through the membrane (or other barrier material). Accordingly, in some embodiments, the protein is pore-forming protein that is part of a nanopore, and/or is part of a multimeric protein complex or assembly that forms a nanopore.
Where the pore-forming protein is α-HL, a heptameric complex of the α-HL monomers can spontaneously form a nanopore in a lipid bilayer. It has been shown that heptamers of α-HL comprising a ratio of 6:1 native α-HL to mutant α-HL can form nanopores (see e.g., Valeva et al. (2001), and references cited therein). Accordingly, in some embodiments, the compositions and methods of the present disclosure can comprise a nanopore, wherein the nanopore comprises a heptameric α-HL complex, which has 6:1 native α-HL to α-HL-C46, and further wherein the α-HL-C46 is conjugated to a biomolecule in carrying out steps (a)-(c). In some embodiments, the biomolecule conjugated to the nanopore is a DNA polymerase.
Further it is contemplated that the site-selective conjugation method comprising steps (a)-(c) can be carried out wherein the protein is a pore-forming protein that is part of a multimeric complex that has formed a nanopore. Thus, in some embodiments, the method of forming the conjugate comprises first forming a nanopore comprising a pore-forming protein then carrying out steps (a)-(c) of the method wherein the pore-forming protein is part of a multimer. Accordingly, in some embodiments, the present disclosure provides a composition comprising a heptameric α-HL nanopore, wherein at least one of the α-HL monomer units is covalently modified as in compounds of formula (II), (IV), and (V). In some embodiments, the heptameric α-HL nanopore comprises 6 native α-HL monomers and 1α-HL mutant monomer that comprises an amino acid residue covalently modified with a click reactive group X, as in the compound of formula (II). In some embodiments, the 1α-HL mutant monomer is α-HL-C46, which comprises a single cysteine residue.
In some embodiments, it is contemplated that the site-selective conjugation method comprising steps (a)-(c) can be carried out wherein the protein is a pore-forming protein that is part of a nanopore that is in solution. However, it is also contemplated that in some embodiments of the conjugation method of steps (a)-(c) can be carried out wherein the pore-forming protein is part of a nanopore that is immobilized, such as through covalent or non-covalent attachment (directly or indirectly) to a solid support.
It is contemplated that nanopores comprising a pore-forming protein conjugate composition of formula (V) of the present disclosure can be used in typical nanopore applications and devices, such as single-molecule nucleic acid sequencing. Nanopore devices and methods for making and using. them are disclosed in e.g., U.S. Pat. Nos. 7,005,264 B2; 7,846,738; 6,617,113: 6,746,594; 6,673,615; 6,627,067; 6,464,842; 6,362,002; 6,267,872; 6,015,714; 5,795,782: and U.S. Publication Nos. 2013/0264207, 2013/0244340, 2004/0121525, and 2003/0104428, each of which are hereby incorporated by reference in their entirety. In such nanopore embodiments, the pore-forming protein typically is embedded in a membrane attached to a solid substrate. Typically, the solid substrate comprises a material selected from the group consisting of polymer, glass, silicon, and a combination thereof. Additionally, the solid substrate can further comprise adjacent to the nanopore, a sensor, a sensing circuit, or an electrode coupled to a sensing circuit, optionally, a complementary metal-oxide semiconductor (CMOS), or field effect transistor (FET) circuit.
Generally, biomolecules useful in the embodiments of the present disclosure can be any protein or nucleic acid that might be desirable to conjugate with a pore-forming protein, and thereby position adjacent to a nanopore, and accompanying nanopore detection system. In one embodiment it is contemplated that the conjugate compositions of the present disclosure can be used in nanopore-based nucleic acid sequencing devices. Accordingly, in some embodiments of the compositions and methods disclosed herein, the biomolecule is an enzyme capable of catalyzing the synthesis of a nucleotide polymer. In some embodiments, the biomolecule is an enzyme selected from the group consisting of a DNA polymerase, RNA polymerase, reverse transcriptase, and DNA ligase. In some embodiments, the biomolecule is a naturally-occurring or non-naturally occurring (e.g., engineered) enzyme that has 5′→3′ DNA polymerase activity and strong strand displacement activity but lacks 5′→3′ exonuclease activity.
A wide range of polymerases and ligases are known in the art, and the conjugation reagents and methods provided herein should be broadly applicable to them due to their common amino acid polymeric structure. Exemplary polymerases that may be used in the compositions and methods of the present disclosure include the nucleic acid polymerases such as DNA polymerase (e.g., enzyme of class EC 2.7.7.7), RNA polymerase (e.g., enzyme of class EC 2.7.7.6 or EC 2.7.7.48), reverse transcriptase (e.g., enzyme of class EC 2.7.7.49), and DNA ligase (e.g., enzyme of class EC 6.5.1.1). In some embodiments, the biomolecule comprises a DNA polymerase from Bacillus stearothermophilus. In some embodiments, the biomolecule comprises the large fragment of DNA polymerase from B. stearothermophilus. In one embodiment, the biomolecule is DNA polymerase Bst 2.0 (commercially available from New England BioLabs, Inc., Massachusetts, USA). In some embodiments, the biomolecule is 9° N polymerase, E. coli DNA Polymerase I, Bacteriophage T4 DNA polymerase, Sequenase, Taq DNA polymerase, 9° N polymerase (exo-)A485L/Y409V or Phi29 DNA polymerase (ϕ29 DNA Polymerase).
In some embodiments, a DNA polymerase useful in the methods and conjugate compositions of the present disclosure is Pol6, which has the following 726 aa sequence:
As described elsewhere herein, a fusion polypeptide of the biomolecule (e.g., DNA polymerase) and a SpyCatcher protein can be used in the methods and compositions of the present disclosure. Accordingly, in some embodiments, a fusion of the SpyCatcher protein sequence with His tag and linker of SEQ ID NO: 8 and the 726 amino acid Pol6 polymerase sequence of SEQ ID NO: 9. One such exemplary fusion polypeptide of DNA polymerase Pol6 and a SpyCatcher protein useful in the methods and compositions of the present disclosure comprises the following 875 amino acid sequence:
The ordinary artisan would recognize that the exemplary 875 aa SpyCatcher-Pol6 fusion polypeptide sequence of SEQ ID NO: 10 can be encoded by any of a broad range of degenerate nucleotide (nt) coding sequences. In one embodiment, the SpyCatcher-Pol6 fusion sequence is encoded by the 2610 nt sequence:
In specific embodiments, the present disclosure provides methods of steps (a)-(c) and associated compositions comprising compounds of formula (I), (II), (III), (IV), and (V), wherein the linkers LA and LB are independently selected from the group consisting of structures of formula (VIa)-formula (VIe) shown below in Table 11.
This example illustrates the use of the site-selective conjugation method of steps (a)-(c) disclosed herein, wherein the B and Z reactive groups undergo a native chemical ligation (NCL) reaction in step (c). The example demonstrates preparation of a composition of formula (V), wherein the cysteine side-chain of an α-HL-C46 pore-forming protein that is part of a heptameric nanopore complex is conjugated to the N-terminus of a DNA polymerase (Pol), as depicted schematically in
A. Pore-forming protein (e.g., α-HL) purification: The pore-forming protein monomers used are native α-HL and an engineered α-HL-C46, both encoded with 6-His tags for purification. The K46C (lysine at position 46 substituted with cysteine) mutant of a S. aureus α-HL monomer with a 6-His tag (“α-HL-C46”) is prepared using standard protein engineering techniques (see e.g., Valeva et al. (2001) and Palmer et al. (1993)). The native α-HL and the α-HL-C46 monomers are recombinantly expressed in E. coli, and affinity purified using standard techniques. Briefly, the wild-type α-HL and α-HL-C46 are purified as described in the protocol for “PrepEase” His-tagged protein purification kits (USB-Affymetrix; USA) and exchanged into 1× PBS with 1 mM tris-carboxyethyl-phosphine (TCEP) at pH 7.2 at 1.0 mg/mL protein concentration. All α-HL purification steps are performed in the presence of reducing agent (TCEP or DTT).
B. 6:1 heptameric nanopore formation: Purified α-HL-C46 is mixed with wild-type α-HL in the presence of lipid to form heptamers as follows. To obtain a heptameric pore complex with the optimal 6:1 ratio of native α-HL monomers to the α-HL-C46 mutant monomer, an 11:1 ratio is used for oligomerization. Lipid (1,2-diphytanoyl-sn-glycero-3-phosphocholine, powder, Avanti Polar Lipids) is added to a final concentration of 5 mg/mL in 50 mM tris, 200 mM NaCl, pH 8.0 for 30 minutes at 40° C.
glucoside (β-OG) is added to pop vesicles, as assessed by clearing, to solubilize the proteins. Then samples are concentrated using 100K MWCO filters and spun at 24000 RPM for 30 minutes to pellet the precipitated protein. After equilibrating size-exclusion columns with 30 mM 130G, 75 mM KCl, 20 mM HEPES at pH 7.5, 500 μL of the concentrated samples are loaded at low pressure to separate heptameric 6:1 α-HL pore complexes from monomers. After concentration to 5 mL in two consecutive size-exclusion columns, the samples are loaded on Mono S 5/50 GL columns (GE Healthcare; New Jersey, USA). Further FPLC is used to separate the 6:1 α-HL:α-HL-C46 pores from those having different subunit stoichiometries (e.g., 7:0, 5:2). The FPLC mobile phase consists of: A, running buffer: 20 mM 2-(N-morpholino)ethanesulfonic acid (MES), 0.1% Tween®20, at pH 5; B, elution buffer: 2M NaCl, 20 mM MES, 0.1% Tween®20 at pH 5. Purification is performed from 100% A isocratic over 21 minutes followed by a linear gradient of 0-100% B for 20 minutes and then 100% B isocratic over another 2 minutes. The flow rate is 1 ml/min. Pure native 7:0 α-HL heptameric pore complex elutes first and the 6:1 α-HL:α-HL-C46 heptameric pore complex eluted with a retention time of from about 24.5 min to about 25.5 min.
C. DBCO-maleimide reagent reaction of step (a) and isolation of DBCO-modified pore-forming protein of formula (II): Reducing agent TCEP or DTT is removed from the purified 6:1 heptameric α-HL nanopore complex by buffer exchange and the pH of the conjugation buffer adjusted to pH 7. DBCO maleimide reagent (Click Chemistry Tools, A108P-100) is dissolved in anhydrous DMF to a concentration of 100 mM. The maleimide reagent is added in 10 fold excess over the protein and the mixture incubated overnight at 4 C. Excess maleimide reagent is separated from the DBCO-modified nanopore reaction mixture by buffer exchange before the next reaction step.
D. Preparation of azide-modified benzyl thioester cognate click reagent of formula (III): The synthesis of the azide thioester cognate click reagent is carried out using the general reaction scheme shown below.
Briefly, solution of azide-PEG4-NHS (0.1 g, 0.00026 mol) in DMF (2 mL) is added dropwise to a solution of benzylmercaptan (36 μL, 0.00031 mol, 1.2 eq) in DMF (3 mL) and triethylamine (108 μL, 0.00077 mol, 3 eq) at room temperature. The resulting reaction mixture is stirred at room temperature (RT) and progress of the reaction is monitored by TLC. Upon completion, this reaction mixture is diluted in dichloromethane and washed with NaHCO3 saturated solution, washed with water 2×100 mL, and then dried (Na2SO4). The resulting oil is separated on flash chromatograph (SiO2 in Hexane:EA mixture 10:1) to produce 0.06 g of product (˜58%) yield. Mass spectra of the resulting azide-modified benzyl thioester has a major ion at 399 (M+1). Azide-modified benzyl thioester compound is dissolved in DMF to a concentration of 147 mM.
E. Click reaction in step (b) of compounds of formula (II) and (III) and isolation/purification of benzyl thioester modified pore-protein of formula (IV): The azide-modified benzyl thioester compound of formula (III) prepared in step D of this Example is added in 10-fold excess to the DBCO-maleimide-modified pore protein nanopore complex prepared in Step C of this Example. The resulting mixture is allowed to react overnight at 4 C. After 18 hours, the benzyl thioester modified pore protein of formula (IV) is separated from excess unreacted compound by buffer exchange (desalting).
F. Native Chemical Ligation (NCL) reaction resulting in site-specific α-HL-polymerase conjugate of formula (V): A Polio DNA polymerase (SEQ ID NO: 9) engineered with an N-terminal cysteine, and the benzyl thioester modified pore protein of formula (IV) prepared in Step E (as a 6:1 nanopore complex), are incubated with the native chemical ligation catalyst, 4-mercaptophenylacetic acid (MPAA) in the relative ratios of 10:1:100 respectively for 18 hours at 4 C. The expected α-HL-polymerase conjugate is characterized by gel electrophoresis and by performing nanopore sequencing experiments as described elsewhere herein
This example illustrates the use of the site-selective conjugation method of steps (a)-(c) disclosed herein with B and Z reactive groups providing a SpyTag peptide to SpyCatcher protein reaction in step (c). The example demonstrates preparation of a composition of formula (V), wherein the SpyTag-modified C46 residue of the α-HL-C46 pore-forming protein, that is part of a heptameric nanopore complex, is site-specifically conjugated to a SpyCatcher-Pol6 DNA polymerase fusion, as is shown schematically in
A. Pore-forming protein (e.g., α-HL) purification: The pore-forming protein monomers used are native α-HL and an engineered α-HL-C46, both encoded with 6-His tags for purification. The K46C (lysine at position 46 substituted with cysteine) mutant of a S. aureus α-HL monomer with a 6-His tag (“α-HL-C46”) is prepared using standard protein engineering techniques (see e.g., Valeva et al. (2001) and Palmer et al. (1993)). The native α-HL and the α-HL-C46 monomers are recombinantly expressed in E. coli, and affinity purified using standard techniques. Briefly, the wild-type α-HL and α-HL-C46 are purified as described in the protocol for “PrepEase” His-tagged protein purification kits (USB-Affymetrix; USA) and exchanged into lx PBS with 1mM tris-carboxyethyl-phosphine (TCEP) at pH 7.2 at 1.0 mg/mL protein concentration. All α-HL purification steps are performed in the presence of reducing agent (TCEP or DTT).
B. 6:1 heptameric nanopore formation: Purified α-HL-C46 is mixed with wild-type α-HL in the presence of lipid to form heptamers as follows. To obtain a heptameric pore complex with the optimal 6:1 ratio of native α-HL monomers to the α-HL-C46 mutant monomer, an 11:1 ratio is used for oligomerization. Lipid (1,2-diphytanoyl-sn-glycero-3-phosphocholine, powder, Avanti Polar Lipids) is added to a final concentration of 5 mg/mL in 50 mM tris, 200 mM NaCl, pH 8.0 for 30 minutes at 40° C. 5% octyl-beta-glucoside (β-OG) is added to pop vesicles, as assessed by clearing, to solubilize the proteins. Then samples are concentrated using 100K MWCO filters and spun at 24000 RPM for 30 minutes to pellet the precipitated protein. After equilibrating size-exclusion columns with 30 mM βOG, 75 mM KCl, 20 mM HEPES at pH 7.5, 500 μL of the concentrated samples are loaded at low pressure to separate heptameric 6:1 α-HL pore complexes from monomers. After concentration to 5 mL in two consecutive size-exclusion columns, the samples are loaded on Mono S 5/50 GL columns (GE Healthcare; New Jersey, USA). Further FPLC is used to separate the 6:1 α-HL:α-HL-C46 pores from those having different subunit stoichiometries (e.g., 7:0, 5:2). The FPLC mobile phase consists of: A, running buffer: 20 mM 2-(N-morpholino)ethanesulfonic acid (MES), 0.1% Tween®20, at pH 5; B, elution buffer: 2M NaCl, 20 mM MES, 0.1% Tween ® 20 at pH 5. Purification is performed from 100% A isocratic over 21 minutes followed by a linear gradient of 0-100% B for 20 minutes and then 100% B isocratic over another 2 minutes. The flow rate is 1 ml/min. Pure native 7:0 α-HL heptameric pore complex elutes first and the 6:1 α-HL:α-HL-C46 heptameric pore complex eluted with a retention time of from about 24.5 min to about 25.5 min.
C. DBCO-maleimide reagent reaction of step (a) and isolation of DBCO-modified pore-forming protein of formula (II): Reducing agent TCEP or DTT is removed from the purified 6:1 heptameric α-HL nanopore complex by buffer exchange and the pH of the conjugation buffer adjusted to pH 7. DBCO maleimide reagent (Click Chemistry Tools, A108P-100) is dissolved in anhydrous DMF to a concentration of 100 mM. The maleimide reagent is added in 10 fold excess over the protein and the mixture incubated overnight at 4 C. Excess maleimide reagent is separated from the DBCO-modified nanopore reaction mixture by buffer exchange before the next reaction step.
D. Preparation of azide-modified SpyTag cognate click reagent of formula (III): The SpyTag peptide amino acid sequence AHIVMVDAYKPTK (SEQ ID NO: 1) with an N-terminal L-azido-homoalanine (“ahA”) residue is synthesized and purified using standard automated peptide synthesis methods. The resulting N-azido-modified SpyTag cognate click reagent of formula (III) has the sequence ahA-AHIVMVDAYKPTK (SEQ ID NO: 4). This SpyTag cognate click reagent is dissolved in 20 mM HEPES buffer pH 7.0 (“conjugation buffer”) for use in the next step.
E. Conditions for click reaction of compounds of formula (II) and (III) in step (b) and any intermediate isolation or purification of the SpyTag modified pore-protein of formula (IV): A 10-fold excess of the SpyTag cognate click reagent (prepared in Step D) is added to the DBCO-modified pore-forming protein (prepared in Step C). The resulting click reaction mixture is allowed to react overnight at 4 C. After 18 hours, the resulting SpyTag-modified pore protein of formula (IV) is separated from any excess unreacted cognate click reagent by buffer exchange (desalting).
F. Preparation of SpyCatcher-Pol6 polymerase fusion protein: The sequence encoding the Pol6 polymerase of SEQ ID NO: 9 is recombinantly modified such that a sequence encoding the SpyCatcher protein sequence of SEQ ID NO: 8 extends from the N-terminus of the polymerase. The resulting SpyCatcher-Pol6 fusion has the amino acid sequence of SEQ ID NO: 10, which includes an N-terminal His tag for affinity purification and a GGS peptide linker between the Pol6 and the SpyCatcher. The fusion construct is encoded by the nucleotide sequence of SEQ ID NO: 11.
G. SpyCatcher-SpyTag conjugation reaction and isolation of the final product conjugate of α-HL-polymerase of formula (V): The nanopore complex including the SpyTag-modified α-HL pore protein (prepared in Step E) is incubated with the SpyCatcher-Pol6 fusion (prepared in Step F) in a 1 to 4 molar ratio overnight at 4 C. The SpyCatcher protein and SpyTag peptide undergo a spontaneous covalent bond-forming reaction between a lysine residue of the SpyCatcher protein and an aspartic acid residue of the SpyTag peptide. This covalent bond formation results in a specific linkage conjugating the Pol6 polymerase to the α-HL-C46 of the heptameric nanopore complex illustrated generically herein by formula (Vm). Formation of the site-specific conjugate is characterized through gel electrophoresis and through use of the conjugate for nanopore sequencing as described in Example 3.
This example illustrates the use of the α-HL-Pol6 nanopore conjugates, prepared as in Example 2, in a nanopore array to sequence a nucleic acid. The α-HL-Pol6 nanopore conjugates are embedded in membranes formed over an array of individually addressable integrated circuit chips. This α-HL-Pol6 nanopore array is exposed to a JAM 1A self-priming DNA template and a set of four differently 5′-tagged nucleotide substrates corresponding to the four nucleotides dA, dC, dG, and dT. As the specific 5′-tagged nucleotide that is complementary to the DNA template is captured and bound to the Pol6 polymerase active site, the “tail” of the tag moiety becomes positioned in the α-HL nanopore conjugated nearby. Under the applied AC potential, the presence of the tag in the pore causes a distinctive blocking current compared to the open pore current (i.e., current with no tag in the nanopore). The sequence of blocking currents measured as the Pol6 synthesizes the strand complementary to the template identifies the sequence of DNA template.
Nanopore detection system: The nanopore blocking current measurements are performed using a nanopore array microchip comprising a CMOS microchip that has an array of 128,000 silver electrodes within shallow wells (chip fabricated by Genia Technologies, Mountain View, CA, USA). Methods for fabricating and using such nanopore array microchips can also be found in U.S. Patent Application Publication Nos. 2013/0244340 A1, US 2013/0264207 A1, and US2014/0134616 A1 each of which is hereby incorporated by reference herein. Each well in the array is manufactured using a standard CMOS process with surface modifications that allow for constant contact with biological reagents and conductive salts. Each well can support a phospholipid bilayer membrane with a nanopore-polymerase conjugate embedded therein. The electrode at each well is individually addressable by computer interface. All reagents used are introduced into a simple flow cell above the array microchip using a computer-controlled syringe pump. The chip supports analog to digital conversion and reports electrical measurements from all electrodes independently at a rate of over 1000 points per second. Nanopore blocking current measurements can be made asynchronously at each of 128K addressable nanopore-containing membranes in the array at least once every millisecond (msec) and recorded on the interfaced computer.
Formation of lipid bilayer on chip: The phospholipid bilayer membrane on the chip is prepared using 1,2-diphytanoyl-sn-glycero-3-phosphocholine (Avanti Polar Lipids). The lipid powder is dissolved in decane at 15 mM and then painted in a layer across the wells on the chip. A thinning process then is initiated by pumping air through the cis side of the array wells, thus reducing multi-lamellar lipid membranes to a single bilayer. Bilayer formation is tested using a ramping voltage from 0 to 1000 mV. A typical single bilayer would temporarily open at an applied voltage of between 300 to 500 mV.
Nanopore-polymerase conjugate insertion in membrane: After the lipid bilayer forms on the wells of the array chip, 3 μM of the 5′-tagged nucleotides, 0.1 μM of a 6:1 α-HL-Pol6 nanopore-polymerase conjugate, 0.4 μM of the desired “JAM1A” DNA template, all in a buffer solution of 3 mM CaCl2, 20 mM Hepes, and 500 mM potassium glutamate, pH 8, at 20° C. is added to the cis side of the chip. The nanopore-polymerase conjugate in the mixture spontaneously inserts into the lipid bilayer. Since only Ca2+ and no Mg2+ metal ion was present, the ternary complex is able to form at the Pol6 active site but the tagged-nucleotide is not incorporated and the 5′-phosphate-linked tag is not released.
The “JAM1A” DNA template is a 99-mer self-priming single-strand that has the sequence 5′-TTTTTGCGCTCGAGATCTCCGTAAGGAGATCTCGAGCGCGGGACTACTACTGGGATCATCAT AGCCACCTCAGCTGCACGTAAGTGCAGCTGAGGTGGC-3′ (SEQ ID NO:12). This DNA template has a first available position on the template for binding to a complementary dT nucleotide.
In the present example, the four tagged nucleotides used as polymerase substrates in the mixture were: dA6P-Cy3-T4-(idSp-T)4-T18-C3 (SEQ ID NO:13), dC6P-Cy3-T30-C3(SEQ ID NO:14), dT6P-Cy3-dT4(N3-CE-dT)3-dT23-C3(SEQ ID NO:15), dG6P-T6-Tmp6-T19-C3 (SEQ ID NO:16). However, a wide range of 5′-tagged nucleotides useful for nanopore devices are available, such as those described in WO 2015/148402, published Oct. 1, 2015, which is hereby incorporated by reference herein for all purposes.
Nanopore blocking current measurements: The buffer solution used as the electrolyte solution for the nanopore current blockade measurements is 500 mM potassium glutamate, pH 8, 3 mM MgCl2, 20 mM Hepes, 5 mM TCEP, at 20° C. A Pt/Ag/AgCl electrode setup is used and an AC current of a −10 mV to 200 mV square waveform applied. AC current can have certain advantages for nanopore detection as it allows for the tag to be repeatedly directed into and then expelled from the nanopore thereby providing more opportunities to detection. AC current also can provide a steadier potential for a more stable current signal and less degradation of the electrodes over time.
Signals representing four distinct current blockade events were observed from the four different 5′-tagged nucleotides as they were captured by the α-HL-Pol6 nanopore-polymerase conjugates primed with the JAM1A DNA template. Plots recorded of the blocking current events were analyzed. Events that last longer than 10 ms and that reduced the open channel current from 0.8 to 0.2 were deemed to indicate productive nucleotide capture by the α-HL-Pol6 nanopore-polymerase conjugate. In three different experiments, the JAM1A DNA sequence was called correctly at rates of 45%, 48%, and 73%, with very low mismatch calls but several regions of incorrect insertion calls. These results indicate that the methods of the present disclosure can provide α-HL-Pol6 nanopore-polymerase conjugates capable of detecting and/or sequencing specific DNA using a nanopore device. Further optimization of array conditions can result in higher correct sequence call rates.
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).
This is a divisional of U.S. application Ser. No. 17/226,378, filed Apr. 9, 2021, which is a divisional of U.S. application Ser. No. 16/134,179, filed Sep. 18, 2018, which is a continuation of International Application No. PCT/EP2017/057002, filed Mar. 23, 2017, and claims the benefit of U.S. Provisional Application No. 62/313,086, filed Mar. 24, 2016, the content of each of which is incorporated by reference in its entirety. This application hereby incorporates-by-reference an ST26 formatted sequence listing having a file name of “04338-5261551_Sequences.xml,” created on Nov. 15, 2023, with a file size of 31,410 bytes. The sequence listing submitted herewith is the ST26 conversion by WIPO Sequence software of the original ST25 formatted sequence listing having a file name of “04338_526US1_SeqListing.txt” created on Sep. 17, 2018, which is 26,320 bytes in size, that was submitted with, and incorporated by reference in, U.S. application Ser. No. 16/134,179, filed Sep. 18, 2018.
| Number | Date | Country | |
|---|---|---|---|
| 62313086 | Mar 2016 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 17226378 | Apr 2021 | US |
| Child | 18511430 | US | |
| Parent | 16134179 | Sep 2018 | US |
| Child | 17226378 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/EP2017/057002 | Mar 2017 | US |
| Child | 16134179 | US |
