Literature DB >> 17545978

Tandem orthogonal proteolysis-activity-based protein profiling (TOP-ABPP)--a general method for mapping sites of probe modification in proteomes.

Eranthie Weerapana1, Anna E Speers, Benjamin F Cravatt.   

Abstract

Activity-based protein profiling (ABPP) utilizes active site-directed chemical probes to monitor the functional state of enzymes directly in native biological systems. Identification of the specific sites of probe labeling on enzymes remains a major challenge in ABPP experiments. In this protocol, we describe an advanced ABPP platform that utilizes a tandem orthogonal proteolysis (TOP) strategy coupled with mass spectrometric analysis to simultaneously identify probe-labeled proteins together with their exact sites of probe modification. Elucidation of probe modification sites reveals fundamental insights into the molecular basis of specific probe-protein interactions. The TOP-ABPP method can be applied to any type of proteomic sample, including those derived from in vitro or in vivo labeling experiments, and is compatible with a variety of chemical probe structures. Completion of the entire protocol, including chemical synthesis of key reagents, requires approximately 8-10 days.

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Year:  2007        PMID: 17545978     DOI: 10.1038/nprot.2007.194

Source DB:  PubMed          Journal:  Nat Protoc        ISSN: 1750-2799            Impact factor:   13.491


  89 in total

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4.  Strategies for discovering and derisking covalent, irreversible enzyme inhibitors.

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Review 6.  Detection of electrophile-sensitive proteins.

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7.  An Activity-Guided Map of Electrophile-Cysteine Interactions in Primary Human T Cells.

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9.  Structure-activity studies of divin: an inhibitor of bacterial cell division.

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10.  Chemical proteomic map of dimethyl fumarate-sensitive cysteines in primary human T cells.

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