Polymerase compositions, methods of making and using same

Abstract

The present disclosure provides compositions, methods, kits, systems and apparatus that are useful for nucleic acid polymerization. In particular, modified polymerases and biologically active fragment thereof are provided that allow for nucleic acid amplification. In one aspect, the disclosure relates to modified polymerases useful for nucleic acid sequencing, genotyping, copy number variation analysis, paired-end sequencing and other forms of genetic analysis. In some aspects, the disclosure relates to modified polymerases useful for the generation of nucleic acid libraries or nucleic acid templates for use in various downstream processes. In some aspects, the disclosure relates to the identification of homologous amino acid mutations that can be transferred across classes or families of polymerases to provide novel polymerases with altered catalytic properties. In some aspects, the disclosure provides modified polymerases having enhanced catalytic properties as compared to a reference polymerase.

1 . A composition comprising an isolated polypeptide having at least 90% identity to SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 15, SEQ ID NO: 18, SEQ ID NO: 19, SEQ ID NO: 20 or SEQ ID NO: 24, or a biologically active fragment thereof. 
     
     
         2 . The composition of  claim 1 , wherein the isolated polypeptide retains polymerase activity. 
     
     
         3 . The composition of  claim 2 , wherein the polymerase activity is selected from DNA binding activity, primer extension activity, strand displacement activity, proofreading activity, nick-initiated polymerase activity, reverse transcriptase activity or nucleotide polymerization activity. 
     
     
         4 . The composition of  claim 1 , wherein, the isolated polypeptide comprises at least 90% identity to SEQ ID NO: 2 and includes one or more amino acid mutations selected from the group consisting of N31R, N31K, D77K, D77H, D113N, D114R, D130A, D130H, D144M, D144K, L212A, E220K, N234R, N234K, V241K, V251K, D264Q, D264S, D264K, Y272R, H273R, L280R, H281A, E294S, E294F, E294G, E294K, V299K, V299H, V299F, D303R, I331Q, E325R, L335T, E336P, I354W, I354F, I370A, Q409R, G416K, V418M, V418I, G420K, D423S, D423K, D423N, D423R, D423T, D423G, D423I, D423K, G425R, Q428W, N429R, N429K, F448K, N457T, A462T, H473R, Y477F, D480R, D480F, D480H, D480A, D480S, D480N, D480Q, N485W, N485Y, N487H, N487W, N487F, N487I, V488R, E493Q, M495Q, V533I, W577Y and D579F. 
     
     
         5 . The composition of  claim 1 , wherein the isolated polypeptide comprises at least 90% identity to SEQ ID NO: 15 and includes one or more amino acid mutations selected from the group consisting of E471K, N485R, R492K, D513K, A675K, D732R, S739W, V740R and E745Q. 
     
     
         6 . The composition of  claim 1 , wherein the isolated polypeptide comprises at least 90% identity to SEQ ID NO: 18 and includes one or more amino acid mutations selected from the group consisting of E245K, S259R, T266K, E290K, A448K, D505R, A512W, R513R and E518Q. 
     
     
         7 . A composition comprising a recombinant polymerase homologous to SEQ ID NO: 1 or a biologically active fragment thereof having at least 90% identity to SEQ ID NO: 1 or a biologically active fragment thereof and wherein the recombinant polymerase comprises a mutation or combination of mutations relative to SEQ ID NO: 1 selected from:
 (a) H46R, wherein the polymerase further includes a mutation at one or more of: E446Q, H572R, H273R, H281A, H473R, Y477F, D480R, or H528A;   (b) E446Q, wherein the polymerase further includes a mutation at one or more of: H46R, H572R, H273R, H281A, H473R, Y477F, D480R, or H528A;   (c) H572R, wherein the polymerase further includes a mutation at one or more of: E446Q, H572R, H273R, H281A, H473R, Y477F, D480R, or H528A;   (d) C93 mutation;   (e) Q238 mutation;   (f) H273 mutation;   (g) H281 mutation;   (h) H473 mutation; and   (i) H528 mutation.   
     
     
         8 . The composition of  claim 7 , wherein the recombinant polymerase homologous to SEQ ID NO: 1 or biologically active fragment thereof comprises any one or more mutations relative to SEQ ID NO: 1 selected from the group consisting of: N31, D77, D113, D114, D130, D144, L212, E220, N234, V241, V251, D264, Y272, H273, L280, H281, E294, V299, D303, I331, E325, L335, E336, I354, I370, Q409, G416, V418, G420, D423, G425, Q428, N429, E446, F448, N457, A462, H473, Y477, D480, N485, N487, V488, E493, M495, H528, V533, H572, W577 and D579. 
     
     
         9 . The composition of  claim 8 , wherein the recombinant polymerase homologous to SEQ ID NO: 1 or biologically active fragment thereof comprises any one or more mutations relative to SEQ ID NO: 1 selected from the group consisting of: N31R, N31K, D77K, D77H, D113N, D114R, D130A, D130H, D144M, D144K, L212A, E220K, N234R, N234K, V241K, V251K, D264Q, D264S, D264K, Y272R, H273R, L280R, H281A, H281M, E294S, E294F, E294G, E294K, V299K, V299H, V299F, D303R, I331Q, E325R, L335T, E336P, I354W, I354F, I370A, Q409R, G416K, V418M, V418I, G420K, D423S, D423K, D423N, D423R, D423T, D423G, D423I, D423K, G425R, Q428W, N429R, N429K, E446Q, F448K, N457T, A462T, H473R, Y477F, D480R, D480F, D480H, D480A, D480S, D480N, D480Q, N485W, N485Y, N487H, N487W, N487F, N487I, V488R, E493Q, M495Q, H528A, H528R, H528K, V533I, H572R, W577Y and D579F. 
     
     
         10 . The composition of  claim 9 , wherein the recombinant polymerase homologous to SEQ ID NO: 1 is any biologically active fragment of the recombinant polymerase that retains polymerase activity. 
     
     
         11 . The composition of  claim 10 , wherein the recombinant polymerase homologous to SEQ ID NO: 1 comprises a mutation that increases dissociation time constant, increases processivity, increases accuracy, increases average read length, increases minimum read length, increases AQ20 or increase 200Q17 value as compared to a reference polymerase lacking a mutation or combination of mutations relative to the recombinant polymerase homologous to SEQ ID NO: 1. 
     
     
         12 . A composition comprising a recombinant polymerase homologous to SEQ ID NO: 15 or a biologically active fragment thereof having at least 90% identity to SEQ ID NO: 15 or a biologically active fragment thereof and wherein the recombinant polymerase comprises a mutation or combination of mutations relative to SEQ ID NO: 15 selected from:
 (a) E471K, wherein the polymerase further includes a mutation at one or more of: N485R, R492K, D513K, A675K, D732R, S739W, V740R and E745Q;   (b) V740R, wherein the polymerase further includes a mutation at one or more of: E471K, N485R, D513K and E745Q;   (c) an N485 mutation;   (d) an D513 mutation;   (e) an D732 mutation; and   (f) an E745 mutation.   
     
     
         13 . The composition of  claim 12 , wherein the recombinant polymerase homologous to SEQ ID NO: 15 or the biologically active fragment thereof comprises: (a) increased accuracy as compared to a reference polymerase lacking a mutation or combination of mutations relative to SEQ ID NO: 15; (b) increased dissociation time constant as compared to a reference polymerase lacking a mutation or combination of mutations relative to SEQ ID NO: 15; (c) increased minimum read length as compared to a reference polymerase lacking a mutation or combination of mutations relative to SEQ ID NO: 15; (d) increased sequencing performance in the presence of a high ionic strength solution as compared to a reference polymerase lacking a mutation or combination of mutations relative to the recombinant polymerase homologous to SEQ ID NO: 15; or (e) increased average read length as compared to a reference polymerase lacking a mutation or combination of mutations relative to SEQ ID NO: 15. 
     
     
         14 . The composition of  claim 12 , wherein the recombinant polymerase homologous to SEQ ID NO: 15 or the biologically active fragment thereof is any biologically active fragment that retains polymerase activity. 
     
     
         15 . The composition of  claim 12 , wherein the recombinant polymerase homologous to SEQ ID NO: 15 comprises a mutation that increases dissociation time constant, increases processivity, increases accuracy, increases average read length, increases minimum read length, increases AQ20 or increase 200Q17 value as compared to a reference polymerase lacking a mutation or combination of mutations relative to the recombinant polymerase homologous to SEQ ID NO: 15. 
     
     
         16 . A composition comprising a recombinant polymerase homologous to SEQ ID NO: 18 or a biologically active fragment thereof having at least 90% identity to SEQ ID NO: 18 or a biologically fragment thereof and wherein the recombinant polymerase comprises a mutation or combination of mutations relative to SEQ ID NO: 18 selected from:
 (a) E245K, wherein the polymerase further includes a mutation at one or more of: S259R, T266K, E290K, A448K, D505R, A512W, R513R and E518Q;   (b) D505R, wherein the polymerase further includes a mutation at one or more of: E245K, S259R, T266K, E290K, A448K, A512W, R513R and E518Q;   (c) an E290 mutation   (d) an 5259 mutation;   (e) an R513 mutation; and   (f) an A512 mutation.   
     
     
         17 . The composition of  claim 16 , wherein the recombinant polymerase homologous to SEQ ID NO: 18 or the biologically active fragment thereof comprises: (a) increased accuracy as compared to a reference polymerase lacking a mutation or combination of mutations relative to SEQ ID NO: 18; (b) increased dissociation time constant activity as compared to a reference polymerase lacking a mutation or combination of mutations relative to SEQ ID NO: 18; (c) increased minimum read length as compared to a reference polymerase lacking a mutation or combination of mutations relative to SEQ ID NO: 18; (d) increased sequencing performance in the presence of high ionic strength as compared to a reference polymerase lacking a mutation or combination of mutations relative to the recombinant polymerase homologous to SEQ ID NO: 18; or (e) increased average read length as compared to a reference polymerase lacking a mutation or combination of mutations relative to SEQ ID NO: 18. 
     
     
         18 . The composition of  claim 16 , wherein the recombinant polymerase homologous to SEQ ID NO: 18 or biologically active fragment thereof is any fragment of the recombinant polymerase that retains polymerase activity. 
     
     
         19 . The composition of  claim 16 , wherein the recombinant polymerase homologous to SEQ ID NO: 18 comprises a mutation that increases dissociation time constant, increases processivity, increases accuracy, increases average read length, increases minimum read length, increases AQ20 or increase 200Q17 value as compared to a reference polymerase lacking a mutation or combination of mutations relative to the recombinant polymerase homologous to SEQ ID NO: 18.