作者: Gabriel Berstein , Jonathan L. Blank , Deok-Young Jhon , John H. Exton , Sue Goo Rhee
DOI: 10.1016/0092-8674(92)90165-9
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摘要: Abstract Purified M1 muscarinic cholinergic receptor and G q/11 were coreconstituted in lipid vesicles. Addition of purified phospholipase C-β1 (PLC-β1) further stimulated the receptor-promoted steady-state GTPase activity up to 20-fold. Stimulation depended upon receptor-mediated GTP-GDP exchange. PLC-β1 caused a rapid burst hydrolysis -bound GTP that was at least 50-fold faster than its absence. Thus, stimulates acts as GTPase-activating protein (GAP) for physiologic regulator, . GTPase-stimulating specific both Such GAP by an effector coupled trimeric can reconcile slow pure proteins vitro with fast deactivation protein-mediated signaling.