IP Library Granted Patent US 7,709,604
Granted Patent B2
US 7,709,604 · App. 11/016,348 · Granted May 4, 2010

Selective incorporation of 5-hydroxytryptophan into proteins in mammalian cells

Assignee: The Scripps Research Institute
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Quick Facts
Patent No.
US 7,709,604
App. No.
11/016,348
Granted
May 4, 2010
Kind
B2
Abstract

This invention provides methods and compositions for incorporation of an unnatural amino acid into a peptide using an orthogonal aminoacyl tRNA synthetase/tRNA pair. In particular, an orthogonal pair is provided to incorporate 5-hydroxy-L-tryptophan in a position encoded by an opal mutation.

Claims (48)

1. A composition comprising:

a eukaryotic translation system;

an orthogonal aminoacyl-tRNA synthetase (O-RS) comprising at least 90% identity to SEQ ID NO: 2 and comprising a proline residue at a position corresponding to position 144 of SEQ ID NO: 2, wherein the O-RS aminoacylates a reference O-tRNA of SEQ ID No: 3 with a 5-substituted tryptophan analog or 5-hydroxy-L-tryptophan (5-HTTP) when the reference O-tRNA and the 5-substituted tryptophan analog or 5-HTTP are present in the translation system; and,

an orthogonal tRNA (O-tRNA) comprising: at least 90% identity to SEQ ID NO: 3, wherein the O-tRNA is aminoacylated with the 5-HTTP by a reference O-RS of SEQ ID NO: 2 when the reference O-RS and the 5-substituted tryptophan analog or 5-HTTP are present in the translation system.

2. The composition of claim 1 , wherein the translation system comprises a cell or an in vitro translation system.

3. The composition of claim 2 , wherein the cell comprises a eukaryotic cell, a Xenopus cell, or a mammalian cell.

4. The composition of claim 1 , wherein the O-RS is encoded by a nucleic acid comprising a polynucleotide sequence selected from the group consisting of: SEQ ID NO: 1 and the complementary polynucleotide sequence thereof.

5. The composition of claim 1 , wherein the O-RS comprises the amino acid sequence of SEQ ID NO: 2.

6. The composition of claim 1 , wherein the O-RS comprises one or more improved or enhanced enzymatic properties, selected from the group consisting of: Km and Kcat, for aminoacylation with the 5-HTPP as compared to a tryptophan.

7. The composition of claim 1 , wherein the O-tRNA is not aminoacylated by an endogenous aminoacyl-tRNA synthetase of the translation system.

8. The composition of claim 1 , wherein the O-tRNA comprises a polynucleotide sequence selected from the group consisting of: SEQ ID NO: 3, SEQ ID NO: 3 with an alternate anticodon and the complementary polynucleotide sequence thereof.

9. The composition of claim 1 , wherein the O-tRNA recognizes a selector codon.

10. The composition of claim 9 , wherein the selector codon comprises a sequence selected from the group consisting of: a four base codon, UAG, UAA and UGA.

11. The composition of claim 1 , further comprising a nucleic acid encoding a product peptide.

12. The composition of claim 11 , wherein the nucleic acid comprises a selector codon sequence recognized by the O-tRNA.

13. The composition of claim 11 , wherein the product peptide comprises an amino acid sequence that is at least 75% identical to that of a wild type therapeutic protein, a diagnostic protein, an industrial enzyme, or a portion thereof.

14. A composition comprising an orthogonal aminoacyl-tRNA synthetase (O-RS), wherein the O-RS preferentially aminoacylates an orthogonal tRNA (O-tRNA) of SEQ ID NO: 3 with a 5-hydroxy-L-tryptophan (5-HTPP), wherein the O-RS comprises an amino acid sequence selected from the group consisting of: SEQ ID NO: 2 and a reference RS comprising at least 90% sequence identity to SEQ ID NO: 2 and comprising a proline residue at a position corresponding to position 144 of SEQ ID NO: 2.

15. The composition of claim 14 , wherein the O-RS comprises one or more improved or enhanced enzymatic properties, selected from the group consisting of: Km and Kcat, for aminoacylation with the 5-HTPP as compared to a tryptophan.

16. The composition of claim 14 , wherein the O-tRNA is not aminoacylated by an endogenous aminoacyl-tRNA synthetase.

17. The composition of claim 14 , further comprising an O-tRNA comprising a polynucleotide sequence selected from the group consisting of: SEQ ID NO: 3; a sequence at least 90% identity to SEQ ID NO: 3 including a suppressor anticodon, a eukaryotic A box transcriptional control element and one or more alternate anticodon, and the complementary polynucleotide sequence thereof.

18. The composition of claim 17 , wherein the O-tRNA recognizes a selector codon.

19. The composition of claim 18 , wherein the selector codon comprises a sequence selected from the group consisting of: a four base codon, UAG, UGA and UAA.

20. The composition of claim 14 , further comprising an endogenous translation system.

21. The composition of claim 20 , wherein the endogenous translation system comprises a cell or an in vitro translation system.

22. The composition of claim 21 , wherein the cell comprises eukaryotic cells or mammalian cells.

23. The composition of claim 14 , further comprising a nucleic acid encoding a product peptide.

24. The composition of claim 23 wherein the nucleic acid comprises a selector codon sequence recognized by the O-tRNA.

25. The composition of claim 23 , wherein the product peptide comprises an amino acid sequence that is at least 75% identical to that of a wild type therapeutic protein, a diagnostic protein, an industrial enzyme, or a portion thereof.

26. A polypeptide comprising an amino acid sequence encoded by a coding polynucleotide sequence, the coding polynucleotide sequence selected from the group consisting of:

a) the coding polynucleotide sequence of SEQ ID NO: 1 and,

b) a coding polynucleotide sequence that encodes a polypeptide selected from the group consisting of SEQ ID NO: 2 and a sequence encoding a polypeptide having at least 90% identity to the polypeptide of SEQ ID NO: 2 and comprising a proline residue at a position corresponding to position 144 of SEQ ID NO: 2, wherein the polypeptide comprises an aminoacyl-tRNA synthetase activity charging a tRNA of SEQ ID NO: 3 with a 5-HTPP.

27. An isolated nucleic acid comprising a polynucleotide sequence selected from the group consisting of:

a) a polynucleotide sequence selected from SEQ ID NO: 3 and,

b) the sequence of (a) comprising at least 90% identity to a reference tRNA of SEQ ID NO: 3 that recognizes a selector codon, or the complementary polynucleotide sequence thereof, wherein an O-RS of SEQ ID NO: 2 charges the nucleic acid with a 5-HTPP.

28. The isolated nucleic acid of claim 27 , wherein the selector codon is selected from the group consisting of: a four base codon, UGA, UAA and UAG.

29. An isolated mammalian cell comprising:

an orthogonal aminoacyl-tRNA synthetase (O-RS), and an orthogonal tRNA (O-tRNA) comprising at least 90% identity to SEQ ID NO:3, wherein the O-tRNA is aminoacylated with a 5-substituted tryptophan analog or 5-hydroxy-L-tryptophan (5-HTTP) by a reference O-RS of SEQ ID NO: 2 when the reference O-RS is present in the translation system,

wherein the O-RS aminoacylates a reference O-tRNA of SEQ ID No: 3 with the 5-substituted tryptophan analog or 5-hydroxy-L-tryptophan (5-HTTP) when the reference O-tRNA and the 5-substituted tryptophan analog or 5-HTTP are present in the translation system, and wherein the O-RS is encoded by a nucleic acid comprising a polynucleotide sequence selected from the group consisting of: SEQ ID NO: 1, a sequence encoding a polypeptide having at least 90% identity to SEQ ID NO: 2 and comprising a proline residue at a position corresponding to position 144 of SEQ ID NO: 2 and the complementary polynucleotide sequence thereof.

30. The mammalian cell of claim 29 , wherein the O-tRNA is not aminoacylated by an endogenous aminoacyl-tRNA synthetase of the cell.

31. The mammalian cell of claim 29 , wherein the O-tRNA comprises a polynucleotide sequence selected from the group consisting of: SEQ ID NO: 3, and the complementary polynucleotide sequence thereof.

32. The composition of claim 1 , wherein the O-tRNA further comprises a suppressor anticodon and a eukaryotic A box transcriptional control element.

33. The composition of claim 32 , wherein the eukaryotic A box transcriptional control element comprises a G at a position corresponding to A7 of SEQ ID NO: 3, a G at a position corresponding to A9 of SEQ ID NO: 3, or a U at a position corresponding to C11 of SEQ ID NO: 3.

34. The composition of claim 1 , wherein the O-tRNA of SEQ ID NO: 3 comprises an acceptor arm sequence.

35. The composition of claim 1 , wherein the O-RS further comprises a His at a position corresponding to position 44 of SEQ ID NO: 2, or an Asp at a position corresponding to position 133 of SEQ ID NO: 2.

36. The composition of claim 1 , wherein the O-RS comprises at least 95% identity to SEQ ID NO: 2.

37. The composition of claim 14 , wherein the O-RS is encoded by a nucleic acid comprising a polynucleotide sequence selected from the group consisting of: SEQ ID NO: 1 and the complementary polynucleotide sequence thereof.

38. The nucleic acid of claim 27 , wherein the nucleic acid of SEQ ID NO: 3 comprises a feature selected from the group consisting of: a suppressor anticodon, a eukaryotic A box transcriptional control element and an acceptor arm sequence.

39. The mammalian cell of claim 29 , wherein the O-tRNA of SEQ ID NO: 3 comprises a suppressor anticodon, a eukaryotic A box transcriptional control element and an acceptor arm sequence.

Assignments (4)
CONFIRMATORY LICENSE Recorded Nov 14, 2008
From: SCRIPPS RESEARCH INSTITUTE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 021840/0499 →
CORRECTION TO THE EXECUTION DATE FOR INVENTOR LITAL ALFONTA Recorded Apr 5, 2005
From: ZHANG, ZHIWEN; ALFONTA, LITAL; SCHULTZ, PETER
To: SCRIPPS RESEARCH INSTITUTE, THE
Reel/Frame 016014/0564 →
CONFIRMATORY LICENSE Recorded Mar 7, 2005
From: SCRIPPS RESEARCH INSTITUTE, THE
To: ENERGY, UNITES STATES DEPARTMENT OF
Reel/Frame 016352/0497 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 3, 2005
From: ZHANG, ZHIWEN; ALFONTA, LITAL; SCHULTZ, PETER
To: SCRIPPS RESEARCH INSTITUTE, THE
Reel/Frame 015832/0331 →
Continuity (3)
Provisional Application 6054876100 · Feb 26, 2004
Provisional Application 6053131200 · Dec 18, 2003
Related Publication 20050136513A1 · Jun 23, 2005