Method for in Vitro Molecular Evolution of Protein Function

• US 20090203572A1
• Filed: 11/17/2006
• Published: 08/13/2009
• Est. Priority Date: 11/19/2005
• Status: Abandoned Application

• Current Assignee: Alligator Bioscience AB
• Original Assignee: Alligator Bioscience AB
• Inventors: Karlsson, Fredrik, Karlsson, Marie, Ellmark, Peter, Haraldsson, Karin, Furebring, Christina, Hager, Ann-Christin Malmborg
• Application Number:
  US12/094,066
• Publication Number:
  US 20090203572A1
• Time in Patent Office: Days
• US Class Current: 514/1.100
• CPC Class Codes: A61P 43/00 Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• CPC Class Codes: C12N 15/1027 by DNA shuffling, e.g. RSR, STEP, RPR

Abstract

The invention provides a method for generating a polynucleotide sequence or population of sequences from parent polynucleotide sequences, the method comprising the steps of (a) providing a first population of polynucleotide molecules and a second population of polynucleotide molecules, the first and second populations together constituting plus and minus strands of parent polynucleotide sequences, (b) digesting the first and second populations of polynucleotide molecules with a nuclease to generate polynucleotide fragments, (c) contacting said polynucleotide fragments generated from the plus strands with fragments generated from the minus strands and (d) amplifying the fragments that anneal to each other to generate at least one polynucleotide sequence encoding one or more protein motifs having an altered amino acid sequence as compared to those encoded by the parent polynucleotides, wherein the degree of sequence variability in a selected region of the at least one polynucleotide molecule produced in step (d) is controlled by the addition of one or more oligonucleotides of predetermined variability, which oligonucleotides anneal to a sequence that lies between, but excludes, the 3′ or 5′ terminal nucleotide of the parent polynucleotide molecule. The invention also provides polynucleotides obtained by the method of the invention and polypeptides encoded by the same.

Claims

1. A method for generating a polynucleotide sequence or population of sequences from parent polynucleotide sequences, the method comprising the steps of

(a) providing a first population of polynucleotide molecules and a second population of polynucleotide molecules, the first and second populations together constituting plus and minus strands of a parent polynucleotide molecule;

(b) digesting the first and second populations of polynucleotide molecules with a nuclease to generate polynucleotide fragments;

(c) contacting said polynucleotide fragments generated from the plus strands with fragments generated from the minus strands (under conditions which permit annealing of fragments); and

(d) amplifying the fragments that anneal to each other to generate at least one polynucleotide molecule which differs in sequence from the parent polynucleotide molecule

wherein the degree of sequence variability in a selected region of the at least one polynucleotide molecule produced in step (d) is controlled by the addition of one or more oligonucleotides of predetermined variability, which oligonucleotides anneal to a sequence that lies between, but excludes, the 3′ and

5′

terminal nucleotides of the parent polynucleotide molecule.

2. The method according to claim 1 wherein the parent polynucleotides encode one or more protein motifs.

3. The method according to claim 1 wherein the first and second populations of polynucleotides are cDNA.

4. The method according to claim 1 wherein the first and second populations of polynucleotides are single-stranded.

5. The method according to claim 1 any wherein the first population of polynucleotides consists of plus strands of parent polynucleotide sequences and second population of polynucleotides consists of minus strands of parent polynucleotide sequences.

6. The method according to claim 1 wherein the first and second populations of polynucleotides are digested separately in step (b).

7. The method according to claim 1 wherein the nuclease in step (b) is an exonuclease.

8. The method according to claim 7 wherein the exonuclease is selected from the group consisting of BAL31, exonuclease I, exonuclease V, exonuclease VII, exonuclease T7 gene 6, bacteriophage lambda exonuclease and exonuclease Rec Jf.

9. The method according to claim 1 wherein the altered amino acid sequence of the at least one polynucleotide sequence produced in step (d) is associated with an altered property of the encoded polypeptide.

10. The method according to claim 4 wherein the oligonucleotides of predetermined variability are added prior to or in step (b) and wherein the nuclease is specific for single-stranded polynucleotides.

11. The method according to claim 1 wherein the oligonucleotides of predetermined variability are added after step (b) and prior to or in step (c).

12. The method according to claim 1 wherein the oligonucleotides of predetermined variability share at least 90% sequence identity with the internal sequence of a parent polynucleotide sequence, for example at least 95%, 96%, 97%, 98%, 99% or 100% sequence identity.

13. The method according to claim 1 wherein the oligonucleotides of predetermined variability share 100% sequence identity with the internal sequence of a parent polynucleotide sequence.

14. The method according to claim 1 wherein the oligonucleotides of predetermined variability are of a single nucleotide sequence.

15. The method according to claim 1 wherein the oligonucleotides of predetermined variability are of at least two different sequences.

16. The method according to claim 15 wherein the oligonucleotides of predetermined variability are variants of the same internal sequence of a parent polynucleotide sequence.

17. The method according to claim 15 wherein the oligonucleotides of predetermined variability share 100% sequence identity with, or are variants of, at least two different regions of the parent polynucleotides.

18. The method according to claim 1 wherein the oligonucleotides of predetermined variability are produced by error-prone PCR or using an oligonucleotide synthesiser.

19. The method according to claim 1 wherein the oligonucleotides of predetermined variability are between 10 and 500 nucleotides in length.

20. The method according to claim 19 wherein the oligonucleotides of predetermined variability are between 50 and 200 nucleotides in length.

21. The method according to claim 1 wherein the parent polynucleotide sequences encode a ligand.

22. The method according to claim 21 wherein the oligonucleotides of predetermined variability share sequence identity with, or are variants of, a region of the parent polynucleotide sequences encoding an amino acid sequence which interacts, directly or indirectly, with a biological molecule.

23. The method according to claim 1 wherein the parent polynucleotide sequences encode an antibody or antibody fragment.

24. The method according to claim 23 wherein the oligonucleotides of predetermined variability share sequence identity with, or are variants of, a region of the parent polynucleotide sequences encoding a framework polypeptide.

25. The method according to claim 23 wherein the oligonucleotides of predetermined variability share sequence identity with, or are variants of, a region of the parent polynucleotide sequences encoding a CDR.

26. The method according to claim 1 wherein the parent polynucleotide sequences encode an enzyme or catalytically-active fragment thereof.

27. The method according to claim 26 wherein the oligonucleotides of predetermined variability share sequence identity with, or are variants of, a region of the parent polynucleotide sequences encoding the active site, a modulatory site or a region involved in enzyme stability.

28. The method according to claim 1 wherein the parent polynucleotide sequences encode an antigen.

29. The method according to claim 28 wherein the oligonucleotides of predetermined variability share sequence identity with, or are variants of, a region of the parent polynucleotide sequences encoding an epitope.

30. The method according to claim 1 wherein step (c) further comprises adding primer sequences that anneal to the 3′

and/or 5′

ends of at least one of the parent polynucleotides under annealing conditions.

31. The method according to claim 1 wherein, in step (b), at least one parameter of the reaction used for digestion of the first population of polynucleotide molecules is different from the equivalent parameter(s) used in the reaction for digestion of the second population of polynucleotide molecules.

32. The method according to claim 31 wherein the reaction parameter is selected from nuclease type, nuclease concentration, reaction volume, duration of the digestion reaction, temperature of the reaction mixture, pH of the reaction mixture, length of parent polynucleotide sequences, the amount of parent polynucleotide molecules and the buffer composition of the reaction mixture.

33. The method according to claim 1 wherein the parent polynucleotide sequences have been subjected to mutagenesis.

34. The method according to claim 1 wherein one or both of the populations of fragments generated in step (b) are subjected to mutagenesis.

35. The method according to claim 33 wherein the mutagenesis is error-prone PCR.

36. The method according to claim 1 wherein step (b) is carried out to generate populations of single-stranded fragments of varying lengths.

37. The method according to claim 36 wherein step (b) is controlled to generate a population of single-stranded fragments having an average length of more than approximately 50 nucleotides.

38. The method according to claim 1 further comprising the step of expressing at least one polynucleotide sequence generated in step (d) to produce the encoded polypeptide.

39. The method according to claim 38 further comprising the step of testing the encoded polypeptide for altered characteristics.

40. A polynucleotide obtained or obtainable by a method according to claim 1.

41. A polynucleotide library comprising a plurality of polynucleotides according to claim 40.

42. A vector comprising a polynucleotide according to claim 40.

43. A method for making a polypeptide having altered properties, the method comprising the following steps:

(a) generating variant forms of a parent polynucleotide using a method according to claim 1;

(b) expressing the variant polynucleotides produced in step (a) to produce variant polypeptides;

(c) screening the variant polypeptides for altered properties; and

(d) selecting a polypeptide having altered properties from the variant polypeptides.

44. A polypeptide obtained or obtainable by a method according to claim 43.

45. A pharmaceutical composition comprising a polynucleotide according to claim 40 and a pharmaceutically acceptable carrier.

48. A process for preparing a pharmaceutical composition which comprises, following the identification of a polynucleotide and/or encoded polypeptide with altered sequence or characteristics by a method according to claim 1, adding said polynucleotide and/or encoded polypeptide to a pharmaceutically acceptable carrier.

49. A method for treating a disease in a patient comprising administering a polynucleotide and/or encoded polypeptide with altered sequence or characteristics by a method according to claim 1.

50. A method for diagnosing a disease in a patient comprising using a polynucleotide and/or encoded polypeptide with altered sequence or characteristics by a method according to claim 1.

51. A method for detecting and/or amplifying a target polynucleotide in a sample using a polynucleotide with an altered sequence according to a method as claimed in claim 1.

54. The method according to claim 34 wherein the mutagenesis is error-prone PCR.

55. A pharmaceutical composition comprising a polypeptide according to claim 44 and a pharmaceutically acceptable carrier.

46. (canceled)

47. (canceled)

52. (canceled)

53. (canceled)