Wilson P T, Lentz T L, Hawrot E
Proc Natl Acad Sci U S A. 1985 Dec;82(24):8790-4. doi: 10.1073/pnas.82.24.8790.
A region of the alpha subunit of the nicotinic acetylcholine receptor containing the alpha-bungarotoxin-binding domain was mapped on the primary amino acid sequence in relation to asparagine-141, the presumed site of N-linked glycosylation. Proteolytic fragments of the alpha subunit, immobilized onto positively charged membrane filters, that bind 125I-labeled bungarotoxin were further analyzed on the basis of the size of the fragments and the presence of asparagine-141 as determined by susceptibility to digestion with endoglycosidase H. The bungarotoxin-binding site was found not to reside between amino acid residues 1 and 140 since bungarotoxin-binding fragments that are considerably larger than 140 amino acids and lack N-linked oligosaccharide chains were detected. The size of the smallest bungarotoxin-binding fragment containing asparagine-141 and the size of fragments produced by digestion with V8 protease further indicated that the bungarotoxin-binding site is contained within amino acid residues 153-241. A 32-amino acid synthetic peptide comprising a portion of this region (residues 173-204) was tested for its ability to bind 125I-labeled bungarotoxin. 125I-labeled bungarotoxin bound to the peptide and was competed by unlabeled bungarotoxin and d-tubocurarine with IC50 values of 0.5 microM and 2 mM, respectively. We conclude that a major determinant of the bungarotoxin-binding site on the alpha subunit resides between residues 173 and 204.
烟碱型乙酰胆碱受体α亚基中包含α-银环蛇毒素结合结构域的区域,相对于天冬酰胺-141(推测的N-连接糖基化位点),在一级氨基酸序列上进行了定位。固定在带正电荷的膜滤器上的α亚基蛋白水解片段,结合125I标记的银环蛇毒素,根据片段大小以及通过内切糖苷酶H消化敏感性确定的天冬酰胺-141的存在情况进行了进一步分析。发现银环蛇毒素结合位点不在氨基酸残基1至140之间,因为检测到了比140个氨基酸大得多且缺乏N-连接寡糖链的银环蛇毒素结合片段。包含天冬酰胺-141的最小银环蛇毒素结合片段的大小以及用V8蛋白酶消化产生的片段大小进一步表明,银环蛇毒素结合位点包含在氨基酸残基153 - 241内。测试了一个包含该区域一部分(残基173 - 204)的32个氨基酸的合成肽结合125I标记的银环蛇毒素的能力。125I标记的银环蛇毒素与该肽结合,并分别被未标记的银环蛇毒素和d - 筒箭毒碱竞争,IC50值分别为0.5 microM和2 mM。我们得出结论,α亚基上银环蛇毒素结合位点的一个主要决定因素位于残基173和204之间。