Wiser O, Trus M, Tobi D, Halevi S, Giladi E, Atlas D
Department of Biological Chemistry, Hebrew University of Jerusalem, Israel.
FEBS Lett. 1996 Jan 22;379(1):15-20. doi: 10.1016/0014-5793(95)01475-6.
The membrane topology of alpha 2/delta subunit was investigated utilizing electrophysiological functional assay and specific anti-alpha 2 antibodies. (a) cRNA encoding a deleted alpha 2/delta subunit was coinjected with alpha 1C subunit of the L-type calcium channel into Xenopus oocytes. The truncated form, lacking the third putative TM domain (alpha 2/delta delta TMIII), failed to amplify the expressed inward currents, normally induced by alpha 1C coinjected with intact alpha 2/delta subunit. Western blot analysis of alpha 2/delta delta TMIII shows the appearance of a degraded alpha 2 protein and no expression of the full-size two-TM truncated-protein. The improper processing of alpha 2/delta delta TMIII suggests that the alpha 2/delta is a single TM domain protein and the TM region is positioned at the delta subunit. (b) External application of anti-alpha 2 antibodies, prepared for an epitope within the alternatively spliced and 'intracellular' region, inhibits depolarization induced secretion in PC12, further supporting an external location of the alpha 2 subunit and establishing delta subunit as the only membrane anchor for the extracellular alpha 2 subunit.
利用电生理功能测定和特异性抗α2抗体研究了α2/δ亚基的膜拓扑结构。(a) 将编码缺失的α2/δ亚基的cRNA与L型钙通道的α1C亚基共注射到非洲爪蟾卵母细胞中。缺少第三个假定跨膜结构域(α2/δΔTMIII)的截短形式未能增强由与完整α2/δ亚基共注射的α1C正常诱导的内向电流。对α2/δΔTMIII的蛋白质免疫印迹分析显示出现了降解的α2蛋白,且未表达全长双跨膜截短蛋白。α2/δΔTMIII的加工不当表明α2/δ是单跨膜结构域蛋白,且跨膜区域位于δ亚基。(b) 对为可变剪接和“细胞内”区域内的一个表位制备的抗α2抗体进行胞外应用,可抑制PC12中去极化诱导的分泌,进一步支持α2亚基位于胞外,并确定δ亚基是胞外α2亚基的唯一膜锚定物。