The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Dec. 15, 2015

Filed:

Nov. 09, 2012
Applicant:

President and Fellows of Harvard College, Cambridge, MA (US);

Inventors:

Adrian Salic, Cambridge, MA (US);

Jing Liu, Brookline, MA (US);

Assignee:
Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
C07D 473/34 (2006.01); C12Q 1/02 (2006.01); C07H 19/16 (2006.01); G01N 33/533 (2006.01); G01N 33/68 (2006.01); A61K 49/00 (2006.01);
U.S. Cl.
CPC ...
C12Q 1/02 (2013.01); A61K 49/0052 (2013.01); A61K 49/0056 (2013.01); C07D 473/34 (2013.01); C07H 19/16 (2013.01); G01N 33/533 (2013.01); G01N 33/68 (2013.01); G01N 2500/10 (2013.01);
Abstract

Synthesis of many proteins is tightly controlled at the level of translation and plays an essential role in fundamental processes such as cell growth and proliferation, signaling, differentiation or death. Methods that allow imaging and identification of nascent proteins allow for dissecting regulation of translation, both spatially and temporally, including in whole organisms. Described herein are robust chemical methods for imaging and affinity-purifying nascent polypeptides in cells and in animals, based on puromycin analogs. Puromycin analogs of the present invention form covalent conjugates with nascent polypeptide chains, which are rapidly turned over by the proteasome and can be visualized and specifically captured by a bioorthogonal reaction (e.g., [3+2] cycloaddition). The methods of the present invention have broad applicability for imaging protein synthesis and for identifying proteins synthesized under various physiological and pathological conditions in vivo.


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