Wiser O, Tobi D, Trus M, Atlas D
Department of Biological Chemistry, The Hebrew University of Jerusalem, Israel.
FEBS Lett. 1997 Mar 10;404(2-3):203-7. doi: 10.1016/s0014-5793(97)00130-0.
The voltage sensitive N-type calcium channel interacts functionally and biochemically with synaptotagmin (p65). N-type channel interaction with p65 is demonstrated in the Xenopus oocyte expression system, where p65 alters the steady state voltage inactivation of the N-channel, and fully restores the syntaxin-modified current amplitude and inactivation kinetics in a calcium dependent manner. In agreement with the functional results, GST-p65 fusion protein binds to a cytosolic region, amino acids 710-1090 of the N-type channel (N-loop(710-1090)). The results of the combined approach provide a functional and biochemical basis for proposing that p65 interaction with the N-type channel brings p65 into a close association with a syntaxin-coupled channel. In turn, calcium entry through the liberated channel initiates fusion of the primed vesicles with the cell membrane at a short distance from the site of calcium entry.
电压敏感型N型钙通道在功能和生化方面与突触结合蛋白(p65)相互作用。在非洲爪蟾卵母细胞表达系统中证实了N型通道与p65的相互作用,其中p65改变了N通道的稳态电压失活,并以钙依赖的方式完全恢复了 syntaxin 修饰的电流幅度和失活动力学。与功能结果一致,GST-p65融合蛋白与N型通道(N环(710-1090))的胞质区域(氨基酸710-1090)结合。综合方法的结果为提出p65与N型通道的相互作用使p65与 syntaxin 偶联通道紧密结合提供了功能和生化基础。反过来,通过释放的通道进入的钙引发了引发的囊泡与距钙进入位点短距离的细胞膜融合。