IP Library Granted Patent US 8,609,344
Granted Patent B2
US 8,609,344 · App. 10/910,718 · Granted Dec 17, 2013

Nucleic-acid programmable protein arrays

Inventors: Joshua Labaer (Medfield, MA); Albert Y. Lau (New York, NY)
Assignee: President and Fellows of Harvard College
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Quick Facts
Patent No.
US 8,609,344
App. No.
10/910,718
Granted
Dec 17, 2013
Kind
B2
Abstract

Arrays of polypeptides are generated by translation of nucleic acid sequences encoding the polypeptides at a plurality of addresses on the array.

Claims (24)

1. A method of evaluating a protein interaction, the method comprising:

providing a substrate with a plurality of addresses, each address comprising (i) a first nucleic acid encoding a hybrid amino acid sequence comprising a first amino acid sequence and an affinity tag, (ii) a binding agent that recognizes the affinity tag, and (iii) a second nucleic acid encoding a second amino acid sequence;

contacting each address of the plurality with a cell-free transcription/translation effector to thereby translate the first nucleic acid and the second nucleic acid;

maintaining the substrate under conditions permissive for the hybrid amino acid sequence to bind the binding agent; and

detecting the presence of the second amino acid sequence at each of the plurality of addresses.

2. A method of evaluating a protein interaction, the method comprising:

providing a substrate with a plurality of addresses, each address comprising (i) a first nucleic acid encoding a hybrid amino acid sequence comprising a first amino acid sequence and an affinity tag, (ii) a binding agent that recognizes the affinity tag, and (iii) a second nucleic acid encoding a second amino acid sequence;

contacting each address of the plurality with a cell-free transcription/translation effector to thereby translate the first nucleic acid and the second nucleic acid;

maintaining the substrate under conditions permissive for the hybrid amino acid sequence to bind the binding agent; and

at each of the plurality of addresses, detecting at least one parameter that is dependent on interaction between a compound that includes the first amino acid sequence and a compound that includes the second amino acid sequence.

3. The method of claim 1 , wherein the first amino acid sequence is common to all addresses of the plurality and the second amino acid sequence is unique among all addresses of the plurality.

4. The method of claim 1 , wherein the first amino acid sequence is unique among all addresses of the pluraity, and the second amino sequence is common to all addresses of the plurality.

5. The method of claim 1 , wherein the second nucleic acid sequence further encodes a polypeptide tag.

6. The method of claim 1 , wherein the second nucleic acid sequence further comprises a recognition tag.

7. The method of claim 1 , further comprising contacting each address of the plurality with a compound to thereby determine if the compound alters the interaction between the first and the second amino acid.

8. The method of claim 1 , wherein the first amino acid sequence is a drug candidate.

9. The method of claim 1 , wherein the first amino acid sequence is a drug target and the second amino acid sequence is a drug candidate.

10. The method of claim 2 , wherein the first amino acid sequence is common to all addresses of the plurality, and the second amino acid sequence is unique among all addresses of the plurality.

11. The method of claim 2 , wherein the first amino acid sequence is unique among all addresses of the plurality, and the second amino acid sequence is common to all addresses of the plurality.

12. The method of claim 2 , wherein the second nucleic acid sequence further encodes a polypeptide tag.

13. The method of claim 2 , wherein the second nucleic acid sequence further encodes a recognition tag.

14. The method of claim 2 , wherein the first amino acid sequence is a drug candidate.

15. The method of claim 2 , wherein the first amino acid sequence is a drug target, and the second amino sequence is a drug candidate.

16. The method of claim 3 , wherein the second nucleic acid sequence further encodes a polypeptide tag, the first amino acid sequence is a drug target, and the second amino acid sequence is a drug candidate.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 22, 2004
From: LABAER, JOSHUA; LAU, ALBERT Y.
To: PRESIDENT AND FELLOWS OF HARVARD COLLEGE
Reel/Frame 015284/0119 →
Continuity (5)
Continuation In Part PCTUS0317979 · Jun 9, 2003
Continuation In Part 10055432 · Jan 22, 2002
Provisional Application 60387034 · Jun 7, 2002
Provisional Application 60263607 · Jan 23, 2001
Related Publication 20050048580A1 · Mar 3, 2005