Weerapana Eranthie, Speers Anna E, Cravatt Benjamin F
Department of Cell Biology, The Skaggs Institute for Chemical Biology, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.
Nat Protoc. 2007;2(6):1414-25. doi: 10.1038/nprot.2007.194.
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.
基于活性的蛋白质谱分析(ABPP)利用活性位点导向化学探针直接在天然生物系统中监测酶的功能状态。在ABPP实验中,鉴定酶上探针标记的特定位点仍然是一个主要挑战。在本方案中,我们描述了一种先进的ABPP平台,该平台利用串联正交蛋白酶解(TOP)策略结合质谱分析,同时鉴定探针标记的蛋白质及其探针修饰的确切位点。阐明探针修饰位点可揭示特定探针-蛋白质相互作用分子基础的基本见解。TOP-ABPP方法可应用于任何类型的蛋白质组学样品,包括来自体外或体内标记实验的样品,并且与多种化学探针结构兼容。完成整个方案,包括关键试剂的化学合成,大约需要8-10天。