Neumann D, Barchan D, Safran A, Gershoni J M, Fuchs S
Proc Natl Acad Sci U S A. 1986 May;83(9):3008-11. doi: 10.1073/pnas.83.9.3008.
Synthetic peptides and their respective antibodies have been used in order to map the alpha-bungarotoxin binding site within the alpha subunit of the acetylcholine receptor. By using antibodies to a synthetic peptide corresponding to residues 169-181 of the alpha subunit, we demonstrate that this sequence is included within the 18-kDa toxin binding fragment previously reported. Furthermore, the 18-kDa fragment was also found to bind a monoclonal antibody (5.5) directed against the cholinergic binding site. Sequential proteolysis of the acetylcholine receptor with trypsin, prior to Staphylococcus aureus V8 protease digestion, resulted in a 15-kDa toxin binding fragment that is included within the 18-kDa fragment but is shorter than it only at its carboxyl terminus. This 15-kDa fragment therefore initiates beyond Asp-152 and terminates in the region of Arg-313/Lys-314. In addition, experiments are reported that indicate that in the intact acetylcholine receptor, Cys-128 and/or Cys-142 are not crosslinked by disulfide bridges with any of the cysteines (at positions 192, 193, and 222) that reside in the 15-kDa toxin binding fragment. Finally, the synthetic dodecapeptide Lys-His-Trp-Val-Tyr-Tyr-Thr-Cys-Cys-Pro-Asp-Thr, which is present in the 15-kDa fragment (corresponding to residues 185-196 of the alpha subunit) was shown to bind alpha-bungarotoxin directly. This binding was completely inhibited by competition with d-tubocurarine.
为了绘制乙酰胆碱受体α亚基内的α-银环蛇毒素结合位点,人们使用了合成肽及其相应抗体。通过使用针对与α亚基169 - 181位残基相对应的合成肽的抗体,我们证明该序列包含在先前报道的18 kDa毒素结合片段内。此外,还发现18 kDa片段也能结合针对胆碱能结合位点的单克隆抗体(5.5)。在用金黄色葡萄球菌V8蛋白酶消化之前,先用胰蛋白酶对乙酰胆碱受体进行顺序蛋白水解,产生了一个15 kDa毒素结合片段,该片段包含在18 kDa片段内,但仅在其羧基末端比18 kDa片段短。因此,这个15 kDa片段起始于天冬氨酸-152之后,终止于精氨酸-313/赖氨酸-314区域。此外,有实验报道表明,在完整的乙酰胆碱受体中,半胱氨酸-128和/或半胱氨酸-142没有与存在于15 kDa毒素结合片段中的任何半胱氨酸(位于192、193和222位)通过二硫键交联。最后,存在于15 kDa片段(对应于α亚基的185 - 196位残基)中的合成十二肽赖氨酸-组氨酸-色氨酸-缬氨酸-酪氨酸-酪氨酸-苏氨酸-半胱氨酸-半胱氨酸-脯氨酸-天冬氨酸-苏氨酸被证明能直接结合α-银环蛇毒素。这种结合可被与筒箭毒碱的竞争完全抑制。