Synip: A novel insulin-regulated syntaxin 4-binding protein mediating GLUT4 translocation in adipocytes

被引:165
作者
Min, J
Okada, S
Kanzaki, M
Elmendorf, JS
Coker, KJ
Ceresa, BP
Syu, LJ
Noda, Y
Saltiel, AR
Pessin, JE [1 ]
机构
[1] Univ Iowa, Dept Physiol & Biophys, Iowa City, IA 52242 USA
[2] Univ Michigan, Sch Med, Dept Physiol, Ann Arbor, MI 48109 USA
[3] Warner Lambert Parke Davis, Parke Davis Pharmaceut Res Div, Dept Cell Biol, Ann Arbor, MI 48105 USA
关键词
D O I
10.1016/S1097-2765(01)80007-1
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
Insulin-stimulated glucose transport and GLUT4 translocation require regulated interactions between the v-SNARE, VAMP2, and the t-SNARE, syntaxin 4. We have isolated a novel syntaxin 4-binding protein, Synip, which specifically interacts with syntaxin 4. Insulin induces a dissociation of the Synip:syntaxin 4 complex due to an apparent decrease in the binding affinity of Synip for syntaxin 4. In contrast, the carboxyterminal domain of Synip does not dissociate from syntaxin 4 in response to insulin stimulation but inhibits glucose transport and GLUT4 translocation. These data implicate Synip as an insulin-regulated syntaxin 4-binding protein directly involved in the control of glucose transport and GLUT4 vesicle translocation.
引用
收藏
页码:751 / 760
页数:10
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