Clathrin-coated vesicles bearing GAIP possess GTPase-activating protein activity in vitro.
Clathrin-coated vesicles bearing GAIP possess GTPase-activating protein activity in vitro.
复制标题
带有 GAIP 的网格蛋白包被的囊泡在体外具有 GTP 酶激活蛋白活性。
DOI:
10.1073/pnas.96.12.6722
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发表时间:
1999
影响因子:
11.1
通讯作者:
Farquhar,MG
中科院分区:
文献类型:
--
作者:
Fischer,T;Elenko,E;McCaffery,JM;DeVries,L;Farquhar,MG
Gα-interacting protein (GAIP) is a member of the RGS (regulators of G protein signaling) family, which serve as GAPs (GTPase-activating proteins) for Gα subunits. Previously, we demonstrated that GAIP is localized on clathrin-coated vesicles (CCVs). Here, we tested whether GAIP-enriched vesicles could accelerate the GTPase activity of Gαiproteins. A rat liver fraction containing vesicular carriers (CV2) was enriched (4.5×) for GAIP by quantitative immunoblotting, and GAIP was detected on some of the vesicles in the CV2 fraction by immunoelectron microscopy. When liver fractions were added to recombinant Gαi3and tested for GAP activity, only the CV2 fraction contained GAP activity. Increasing amounts of CV2 increased the activity, whereas immunodepletion of the CV2 fraction with an antibody against the C terminus of GAIP decreased GAP activity. CCV fractions were prepared from rat liver by using a protocol that maintains the clathrin coats. GAIP was enriched in these fractions and was detected on CCVs by immunogold labeling. Addition of increasing amounts of CCV to recombinant Gαi3protein increased the GTPase activity. We conclude that CCVs possess GAP activity for Gαi3and that membrane-associated GAIP is capable of interacting with Gαi3. The reconstitution of the interaction between a heterotrimeric G protein and GAIP on CCVs provides biochemical evidence for a model whereby the G protein and its GAP are compartmentalized on different membranes and come into contact at the time of vesicle fusion. Alternatively, they may be located on the same membrane and segregate at the time of vesicle budding.