IP Library Granted Patent US 7,888,063
Granted Patent B2
US 7,888,063 · App. 10/826,919 · Granted Feb 15, 2011

Unnatural reactive amino acid genetic code additions

Assignee: The Scripps Research Institute
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Quick Facts
Patent No.
US 7,888,063
App. No.
10/826,919
Granted
Feb 15, 2011
Kind
B2
Abstract

This invention provides compositions and methods for producing translational components that expand the number of genetically encoded amino acids in eukaryotic cells. The components include orthogonal tRNAs, orthogonal aminoacyl-tRNA synthetases, orthogonal pairs of tRNAs/synthetases and unnatural amino acids. Proteins and methods of producing proteins with unnatural amino acids in eukaryotic cells are also provided.

Claims (18)

1. A method of producing in a eukaryotic cell at least one protein comprising at least one unnatural amino acid, the method comprising:

growing, in an appropriate medium, a eukaryotic cell that comprises a nucleic acid that comprises at least one selector codon and encodes the protein; wherein the medium comprises an unnatural amino acid and the eukaryotic cell comprises:

an orthogonal tRNA (O-tRNA) that functions in the cell and recognizes the selector codon; and,

an orthogonal aminoacyl tRNA synthetase (O-RS) that preferentially aminoacylates the O-tRNA with the unnatural amino acid, wherein the O-RS comprises the amino acid sequence of any one of SEQ ID NOs: 48-53.

2. A method of producing in a eukaryotic cell at least one protein comprising at least one unnatural amino acid, the method comprising:

growing, in an appropriate medium, a eukaryotic cell that comprises a nucleic acid that comprises at least one selector codon and encodes the protein; wherein the medium comprises the unnatural amino acid and the eukaryotic cell comprises an orthogonal tRNA (O-tRNA) that functions in the cell and recognizes the selector codon and an orthogonal aminoacyl tRNA synthetase (O-RS) that preferentially aminoacylates the O-tRNA with the unnatural amino acid, wherein the O-RS is:

(i) a p-propargyloxyphenylalanine O-RS that preferentially aminoacylates the O-tRNA with a p-propargyloxyphenylalanine, or

(ii) a p-azido-L-phenylalanine O-RS that preferentially aminoacylates the O-tRNA with a p-azido-L-phenylalanine, the p-azido-L-phenylalanine O-RS comprising:

(i) an amino acid sequence set forth in any one of SEQ ID NOs: 48-53 and or a conservative variant thereof, wherein the conservative variant is at least 95% identical to any one of SEQ ID NOs: 48-53, and comprises two or more amino acids selected from the group consisting of: glycine, serine, or alanine at a position corresponding to Tyr37; aspartate at a position corresponding to Asn126; asparagine at a position corresponding to Asp182; alanine, or valine, at a position corresponding to Phe183; and, methionine, valine, cysteine, or threonine, at a position corresponding to Leu186; or

(ii) an amino acid sequence that is a conservative variant of SEQ ID NO: 2, which conservative variant is at least 98% identical to SEQ ID NO: 2 and comprises two or more amino acids selected from the group consisting of: glycine, serine, or alanine at a position corresponding to Tyr37; aspartate at a position corresponding to Asn126; asparagine at a position corresponding to Asp182; alanine, or valine, at a position corresponding to Phe183; and, methionine, valine, cysteine, or threonine, at a position corresponding to Leu186; and,

incorporating into the protein the unnatural amino acid in the eukaryotic cell, wherein the unnatural amino acid comprises a first reactive group.

3. The method of claim 2 , wherein the method further comprises contacting the protein with a molecule that comprises a second reactive group; wherein the first reactive group reacts with the second reactive group to attach the molecule to the unnatural amino acid through a [3+2] cycloaddition, thereby modifying the protein.

4. The method of claim 3 , wherein the molecule is a dye, a polymer, a derivative of polyethylene glycol, a photocrosslinker, a cytotoxic compound, an affinity label, a derivative of biotin, a resin, a second protein or polypeptide, a metal chelator, a cofactor, a fatty acid, a carbohydrate, or a polynucleotide.

5. The method of claim 3 , wherein the O-RS is the p-propargyloxyphenylalanine O-RS, the unnatural amino acid is p-propargyloxyphenylalanine, the first reactive group is an alkynyl moiety and the second reactive group is an azido moiety.

6. The method of claim 2 , wherein the unnatural amino acid comprises a p-propargyloxyphenylalanine.

7. The method of claim 3 , wherein the O-RS is the p-azido-L-phenylalanine O-RS, the unnatural amino acid is p-azido-L-phenylalanine, the first reactive group is an azido moiety, and the second reactive group is an alkynyl moiety.

8. The method of claim 2 , wherein the unnatural amino acid comprises a p-azido-L-phenylalanine.

9. The method according to claim 2 , wherein the eukaryotic cell is a yeast cell and wherein the O-tRNA and the O-RS are derived from E. coli.

Assignments (3)
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 021839/0648 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 10, 2004
From: SCRIPPS RESEARCH ISNTITUTE, THE
To: ENERGY, UNITED STATES DEPARTMENT OF
Reel/Frame 015772/0856 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 22, 2004
From: DEITER, ALEXANDER; CROPP, T. ASHTON; CHIN, JASON W.; ANDERSON, J. CHRISTOPHER; SCHULTZ, PETER G.
To: SCRIPPS RESEARCH INSTITUTE, THE
Reel/Frame 014888/0599 →
Continuity (4)
Provisional Application 60479931 · Jun 18, 2003
Provisional Application 60493014 · Aug 5, 2003
Provisional Application 60496548 · Aug 19, 2003
Related Publication 20040265952A1 · Dec 30, 2004