Probing adenylation: using a fluorescently labelled ATP probe to directly label and immunoprecipitate VopS substrates

被引:27
|
作者
Lewallen, Daniel M. [1 ]
Steckler, Caitlin J. [2 ]
Knuckley, Bryan [1 ]
Chalmers, Michael J. [2 ]
Thompson, Paul R. [1 ]
机构
[1] Scripps Florida, Scripps Res Inst, Dept Chem, Jupiter, FL 33458 USA
[2] Scripps Florida, Scripps Res Inst, Dept Mol Therapeut, Jupiter, FL 33458 USA
关键词
GLUTAMINE-SYNTHETASE; AMPYLATION; PROTEINS; BINDING; UBIQUITIN; ENZYME;
D O I
10.1039/c2mb25053e
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The bacterial effector VopS from Vibrio parahaemolyticus modifies host Rho GTPases to prevent downstream signalling, which leads to cell rounding and eventually apoptosis. While previous studies have used [alpha-P-32] ATP for studying this enzyme, we sought to develop a non-radioactive chemical probe of VopS function. To guide these studies, the kinetic parameters were determined for a variety of nucleotides and the results indicated that the C6 position of adenosine was amenable to modification. Since F1-ATP is a commercially available ATP analogue that is fluorescently tagged at the C6 position, we tested it as a VopS substrate, and the results show that VopS uses F1-ATP to label Cdc42 in vitro and in MCF7 whole cell extracts. The utility of this probe was further demonstrated by immunoprecipitating F1-ATP labeled Cdc42 as well as several novel substrate proteins. The proteins, which were identified by LC-MS/MS, include the small GTPases Rac1 and Cdc42 as well as several proteins that are potential VopS substrates and may be important for V. parahaemolyticus pathology. In total, these studies identify F1-ATP as a valuable chemical probe of protein AMPylation.
引用
收藏
页码:1701 / 1706
页数:6
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