Enzymes resistant to photodamage
US-9127259-B2 · Sep 8, 2015 · US
US11377644B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11377644-B2 |
| Application number | US-202017025722-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 18, 2020 |
| Priority date | Feb 1, 2012 |
| Publication date | Jul 5, 2022 |
| Grant date | Jul 5, 2022 |
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Provided are compositions comprising recombinant DNA polymerases that include amino acid substitutions, insertions, deletions, and/or exogenous features that confer modified properties upon the polymerase for enhanced single molecule sequencing. Such properties include increased resistance to photodamage, and can also include enhanced metal ion coordination, reduced exonuclease activity, reduced reaction rates at one or more steps of the polymerase kinetic cycle, decreased branching fraction, altered cofactor selectivity, increased yield, increased thermostability, increased accuracy, increased speed, increased readlength, and the like. Also provided are nucleic acids which encode the polymerases with the aforementioned phenotypes, as well as methods of using such polymerases to make a DNA or to sequence a DNA template.
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What is claimed is: 1. A composition comprising a Φ29-type (phi29-type) recombinant DNA polymerase, which recombinant polymerase comprises an amino acid sequence that is at least 85% identical to SEQ ID NO:1, and which recombinant polymerase comprises one or more mutation selected from the group consisting of an amino acid substitution at position S10, an amino acid substitution at position E244, an amino acid substitution at position A444, an amino acid substitution at position I460, a T231S substitution, a K361R substitution, a T573E substitution, a T573G substitution, and a T573S substitution, wherein identification of positions is relative to SEQ ID NO:1, and wherein said polymerase exhibits polymerase activity. 2. The composition of claim 1 , wherein the recombinant polymerase comprises one or more mutation selected from the group consisting of an S10V substitution, an E244K substitution, an E244Q substitution, an E244R substitution, an A444G substitution, an A444L substitution, an A444S substitution, an A444V substitution, an I460F substitution, an I460L substitution, and an I460V substitution, wherein identification of positions is relative to SEQ ID NO:1. 3. The composition of claim 1 , wherein the recombinant polymerase comprises one or more mutation or combination of mutations selected from the group consisting of an amino acid substitution at position 253, an amino acid substitution at position 375, an amino acid substitution at position 484, an amino acid substitution at position 512, an amino acid substitution at position 510, an amino acid substitution at position 148, an amino acid substitution at position 224, an amino acid substitution at position 239, an amino acid substitution at position 250, an amino acid substitution at position 437, an amino acid substitution at position 235, an amino acid substitution at position 515, an amino acid substitution at position 141, an amino acid substitution at position 142, an amino acid substitution at position 504, an amino acid substitution at position 508, an amino acid substitution at position 513, an amino acid substitution at position 523, an amino acid substitution at position 536, an amino acid substitution at position 539, an amino acid substitution at position 205, an amino acid substitution at position 472, an amino acid substitution at position 437 and an amino acid substitution at position 253, an amino acid substitution at position 508 and an amino acid substitution at position 510, an A437G substitution and an L253H substitution, an A437G substitution and an L253C substitution, a V250A substitution and an L253H substitution, an A437G substitution, a D235E substitution, an E515Q substitution, an E515P substitution, an E515K substitution, a V250A substitution, a V250I substitution, a Y148I substitution, a Y224K substitution, an E239G substitution, a V141K substitution, an L142K substitution, an E508K substitution, an E508K substitution and a D510S substitution, a K536Q substitution, a K539Q substitution, a K205E substitution, a K205D substitution, a K205A substitution, a K472A substitution, an E375Y substitution, a K512Y substitution, an A484E substitution, an L253A substitution, an L253C substitution, an L253S substitution, an L253H substitution, and a D510K substitution, wherein identification of positions is relative to SEQ ID NO:1. 4. The composition of claim 1 , wherein the recombinant polymerase comprises E375Y, A484E, and K512Y substitutions, wherein identification of positions is relative to SEQ ID NO:1. 5. The composition of claim 1 , where the recombinant polymerase comprises an amino acid sequence that is at least 90% identical to SEQ ID NO:1. 6. The composition of claim 1 , wherein the recombinant polymerase comprises one or more exogenous features at the C-terminal and/or N-terminal region of the polymerase. 7. The composition of claim 6 , wherein the recombinant polymerase comprises a biotin ligase recognition sequence and a polyhistidine tag. 8. The composition of claim 6 , wherein the C-terminal region of the recombinant polymerase comprises a His10 tag. 9. The composition of claim 1 , comprising a phosphate-labeled nucleotide analog. 10. The composition of claim 9 , wherein the nucleotide analog comprises a fluorophore. 11. The composition of claim 1 , comprising a phosphate-labeled nucleotide analog and a DNA template, wherein the recombinant polymerase incorporates the nucleotide analog into a copy nucleic acid in response to the DNA template. 12. The composition of claim 1 , wherein the composition is present in a DNA sequencing system. 13. The composition of claim 12 , wherein the sequencing system comprises a zero-mode waveguide. 14. The composition of claim 13 , wherein the recombinant polymerase is immobilized on a surface of the zero-mode waveguide in an active form. 15. A method of sequencing a DNA template, the method comprising: a) providing a reaction mixture comprising: the DNA template, a replication initiating moiety that complexes with or is integral to the template, the recombinant polymerase of claim 1 , wherein the polymerase is capable of replicating at least a portion of the template using the moiety in a template-dependent polymerization reaction, and one or more nucleotides and/or nucleotide analogs; b) subjecting the reaction mixture to a polymerization reaction in which the modified recombinant polymerase replicates at least a portion of the template in a template-dependent manner, whereby the one or more nucleotides and/or nucleotide analogs are incorporated into the resulting DNA; and c) identifying a time sequence of incorporation of the one or more nucleotides and/or nucleotide analogs into the resulting DNA. 16. The method of claim 15 , wherein the subjecting and identifying steps are performed in a zero mode waveguide. 17. A method of making a DNA, the method comprising: (a) providing a reaction mixture comprising: a template, a replication initiating moiety that complexes with or is integral to the template, the recombinant polymerase of claim 1 , which polymerase is capable of replicating at least a portion of the template using the moiety in a template-dependent polymerase reaction, and one or more nucleotides and/or nucleotide analogs; and (b) reacting the mixture such that the polymerase replicates at least a portion of the template in a template-dependent manner, whereby the one or more nucleotides and/or nucleotide analogs are incorporated into the resulting DNA. 18. The method of claim 17 , wherein the mixture is reacted in a zero mode waveguide. 19. The method of claim 17 , the method comprising detecting incorporation of at least one of the nucleotides and/or nucleotide analogs.
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