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PMID: 17545978 Published · ppublish English Journal Article

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

Nature protocols ·Vol. 2 ·No. 6 ·2007-00-00 ·Pages 1414-25

Weerapana E, Speers AE, Cravatt BF

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.

MeSH Terms
Animals Biotin Gene Expression Profiling/methods Mice Molecular Probes Myocardium/metabolism Protein Conformation Proteome/analysis Proteomics/methods
Chemicals
Molecular Probes Proteome Biotin
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Weerapana Eranthie
Department of Cell Biology, The Skaggs Institute for Chemical Biology, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.
Speers Anna E
Cravatt Benjamin F
Article Info
Journal
Nature protocols
Abbr.
Nat Protoc
ISSN
1750-2799
Published
2007-00-00
Pages
1414-25
Language
English
Region
England
NLM ID
101284307
Subset
IM
Grants
NCI NIH HHS · R01 CA087660 · United States
NCI NIH HHS · R01 CA087660-07 · United States
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