Literature DB >> 18366325

Activity-based protein profiling: from enzyme chemistry to proteomic chemistry.

Benjamin F Cravatt1, Aaron T Wright, John W Kozarich.   

Abstract

Genome sequencing projects have provided researchers with a complete inventory of the predicted proteins produced by eukaryotic and prokaryotic organisms. Assignment of functions to these proteins represents one of the principal challenges for the field of proteomics. Activity-based protein profiling (ABPP) has emerged as a powerful chemical proteomic strategy to characterize enzyme function directly in native biological systems on a global scale. Here, we review the basic technology of ABPP, the enzyme classes addressable by this method, and the biological discoveries attributable to its application.

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Year:  2008        PMID: 18366325     DOI: 10.1146/annurev.biochem.75.101304.124125

Source DB:  PubMed          Journal:  Annu Rev Biochem        ISSN: 0066-4154            Impact factor:   23.643


  374 in total

1.  An activity-based imaging probe for the integral membrane hydrolase KIAA1363.

Authors:  Jae Won Chang; Raymond E Moellering; Benjamin F Cravatt
Journal:  Angew Chem Int Ed Engl       Date:  2011-12-07       Impact factor: 15.336

2.  On the mechanism of dimethylarginine dimethylaminohydrolase inactivation by 4-halopyridines.

Authors:  Corey M Johnson; Arthur F Monzingo; Zhihong Ke; Dae-Wi Yoon; Thomas W Linsky; Hua Guo; Jon D Robertus; Walter Fast
Journal:  J Am Chem Soc       Date:  2011-06-23       Impact factor: 15.419

3.  Phosphatidylinositol 3,4,5-trisphosphate activity probes for the labeling and proteomic characterization of protein binding partners.

Authors:  Meng M Rowland; Heidi E Bostic; Denghuang Gong; Anna E Speers; Nathan Lucas; Wonhwa Cho; Benjamin F Cravatt; Michael D Best
Journal:  Biochemistry       Date:  2011-11-30       Impact factor: 3.162

4.  A potent and selective inhibitor of KIAA1363/AADACL1 that impairs prostate cancer pathogenesis.

Authors:  Jae Won Chang; Daniel K Nomura; Benjamin F Cravatt
Journal:  Chem Biol       Date:  2011-04-22

5.  Competitive activity-based protein profiling identifies aza-β-lactams as a versatile chemotype for serine hydrolase inhibition.

Authors:  Andrea M Zuhl; Justin T Mohr; Daniel A Bachovchin; Sherry Niessen; Ku-Lung Hsu; Jacob M Berlin; Maximilian Dochnahl; María P López-Alberca; Gregory C Fu; Benjamin F Cravatt
Journal:  J Am Chem Soc       Date:  2012-03-08       Impact factor: 15.419

Review 6.  The pharmacological landscape and therapeutic potential of serine hydrolases.

Authors:  Daniel A Bachovchin; Benjamin F Cravatt
Journal:  Nat Rev Drug Discov       Date:  2012-01-03       Impact factor: 84.694

7.  Clickable, photoreactive inhibitors to probe the active site microenvironment of fatty acid amide hydrolase().

Authors:  Susanna M Saario; Michele K McKinney; Anna E Speers; Chu Wang; Benjamin F Cravatt
Journal:  Chem Sci       Date:  2011-08-11       Impact factor: 9.825

Review 8.  The grand challenge to decipher the cancer proteome.

Authors:  Samir Hanash; Ayumu Taguchi
Journal:  Nat Rev Cancer       Date:  2010-09       Impact factor: 60.716

Review 9.  The Paracaspase MALT1.

Authors:  Janna Hachmann; Guy S Salvesen
Journal:  Biochimie       Date:  2015-09-16       Impact factor: 4.079

10.  Application of activity-based protein profiling to study enzyme function in adipocytes.

Authors:  Andrea Galmozzi; Eduardo Dominguez; Benjamin F Cravatt; Enrique Saez
Journal:  Methods Enzymol       Date:  2014       Impact factor: 1.600

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