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首页> 外文期刊>Molecular cell >Synip: a novel insulin-regulated syntaxin 4-binding protein mediating GLUT4 translocation in adipocytes.
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Synip: a novel insulin-regulated syntaxin 4-binding protein mediating GLUT4 translocation in adipocytes.

机译:Synip:介导脂肪细胞中GLUT4易位的新型胰岛素调节syntaxin 4结合蛋白。

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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.
机译:胰岛素刺激的葡萄糖转运和GLUT4易位需要v-SNARE,VAMP2和t-SNARE,syntaxin 4之间的调节相互作用。我们已经分离出一种新颖的,与syntaxin 4相互作用的,与syntaxin 4结合的蛋白Synip。由于Synip对syntaxin 4的结合亲和力明显降低,导致Synip:syntaxin 4复合体解离。相反,Synip的羧基末端结构域并未响应胰岛素刺激而与syntaxin 4解离,但抑制了葡萄糖转运和GLUT4易位。这些数据暗示Synip作为胰岛素调节的syntaxin 4结合蛋白,直接参与葡萄糖转运和GLUT4囊泡移位的控制。

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