Recombinant polymerases with increased phototolerance

Abstract

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.

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 80% 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 S194, an amino acid substitution at position Y439, an amino acid substitution at position T441, an amino acid substitution at position A447, an amino acid substitution at position S527, L142R substitution, a D510Q substitution, an S194A substitution, an S194T substitution, a Y439E substitution, a Y439A substitution, a Y439K substitution, and a D523H 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 a T441I substitution, a T441L substitution, and an S527K 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 selected from the group consisting of an S194A substitution, an S194T substitution, a Y439E substitution, a Y439A substitution, a Y439K substitution, a T441G substitution, a T441V substitution, a T441N substitution, a T441A substitution, an A447L substitution, an A447E substitution, an S527E substitution, and an S527N substitution, wherein identification of positions is relative to SEQ ID NO:1. 
     
     
       4. 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. 
     
     
       5. 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. 
     
     
       6. 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. 
     
     
       7. The composition of  claim 1 , A composition comprising a φ29-type (phi29-type) recombinant DNA polymerase, which recombinant polymerase comprises an amino acid sequence that is at least 80% 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 S194, an amino acid substitution at position Y439, an amino acid substitution at position T441, an amino acid substitution at position A447, an amino acid substitution at position S527, an L142R substitution, and a D523H substitution, wherein identification of positions is relative to SEQ ID NO:1, and wherein said polymerase exhibits polymerase activity, wherein the recombinant polymerase comprises one or more exogenous features at the C-terminal and/or N-terminal region of the polymerase. 
     
     
       8. The composition of  claim 7 , wherein the recombinant polymerase comprises a biotin ligase recognition sequence and a polyhistidine tag. 
     
     
       9. The composition of  claim 7 , wherein the C-terminal region of the recombinant polymerase comprises a His10 tag. 
     
     
       10. The composition of  claim 1 , A composition comprising a phosphate-labeled nucleotide analog  and a φ29-type (phi29-type) recombinant DNA polymerase, which recombinant polymerase comprises an amino acid sequence that is at least 80% 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 S194, an amino acid substitution at position Y439, an amino acid substitution at position T441, an amino acid substitution at position A447, an amino acid substitution at position S527, an L142R substitution, and a D523H substitution, wherein identification of positions is relative to SEQ ID NO:1, and wherein said polymerase exhibits polymerase activity. 
     
     
       11. The composition of  claim 10 , wherein the nucleotide analog comprises a fluorophore. 
     
     
       12. The composition of claim  1  10, 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. 
     
     
       13. The composition of  claim 1 , A composition comprising a φ29-type (phi29-type) recombinant DNA polymerase, which recombinant polymerase comprises an amino acid sequence that is at least 80% 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 S194, an amino acid substitution at position Y439, an amino acid substitution at position T441, an amino acid substitution at position A447, an amino acid substitution at position S527, an L142R substitution, and a D523H substitution, wherein identification of positions is relative to SEQ ID NO:1, and wherein said polymerase exhibits polymerase activity, wherein the composition is present in a DNA sequencing system. 
     
     
       14. The composition of  claim 13 , wherein the sequencing system comprises a zero-mode waveguide. 
     
     
       15. The composition of  claim 14 , wherein the recombinant polymerase is immobilized on a surface of the zero-mode waveguide in an active form. 
     
     
       16. 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 ,a φ29-type (phi29-type) recombinant DNA polymerase, which recombinant polymerase comprises an amino acid sequence that is at least 80% 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 S194, an amino acid substitution at position Y439, an amino acid substitution at position T441, an amino acid substitution at position A447, an amino acid substitution at position S527, an L142R substitution, and a D523H substitution, wherein identification of positions is relative to SEQ ID NO:1, and wherein said polymerase exhibits polymerase activity, 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. 
 
     
     
       17. The method of  claim 16 , wherein the subjecting and identifying steps are performed in a zero mode waveguide. 
     
     
       18. 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. 
 
     
     
       19. The method of  claim 18 , wherein the mixture is reacted in a zero mode waveguide. 
     
     
       20. The method of  claim 18 , the method comprising detecting incorporation of at least one of the nucleotides and/or nucleotide analogs.