Literature DB >> 18282485

Proteomic methods for drug target discovery.

Lekha Sleno1, Andrew Emili.   

Abstract

The field of drug target discovery is currently very popular with a great potential for advancing biomedical research and chemical genomics. Innovative strategies have been developed to aid the process of target identification, either by elucidating the primary mechanism-of-action of a drug, by understanding side effects involving unanticipated 'off-target' interactions, or by finding new potential therapeutic value for an established drug. Several promising proteomic methods have been introduced for directly isolating and identifying the protein targets of interest that are bound by active small molecules or for visualizing enzyme activities affected by drug treatment. Significant progress has been made in this rapidly advancing field, speeding the clinical validation of drug candidates and the discovery of the novel targets for lead compounds developed using cell-based phenotypic screens. Using these proteomic methods, further insight into drug activity and toxicity can be ascertained.

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Year:  2008        PMID: 18282485     DOI: 10.1016/j.cbpa.2008.01.022

Source DB:  PubMed          Journal:  Curr Opin Chem Biol        ISSN: 1367-5931            Impact factor:   8.822


  24 in total

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Review 7.  High-throughput screening and small animal models, where are we?

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8.  Small molecule screen for compounds that affect vascular development in the zebrafish retina.

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9.  Knowledge-guided inference of domain-domain interactions from incomplete protein-protein interaction networks.

Authors:  Mei Liu; Xue-Wen Chen; Raja Jothi
Journal:  Bioinformatics       Date:  2009-08-10       Impact factor: 6.937

Review 10.  Systematizing serendipity for cardiovascular drug discovery.

Authors:  Peter J Schlueter; Randall T Peterson
Journal:  Circulation       Date:  2009-07-21       Impact factor: 29.690

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