4.7 Article

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

Journal

NATURE PROTOCOLS
Volume 2, Issue 6, Pages 1414-1425

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nprot.2007.194

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Funding

  1. NCI NIH HHS [R01 CA087660, R01 CA087660-07] Funding Source: Medline
  2. NATIONAL CANCER INSTITUTE [R01CA087660] Funding Source: NIH RePORTER

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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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