Tejedor F J, Catterall W A
Department of Pharmacology, University of Washington, Seattle 98195.
Proc Natl Acad Sci U S A. 1988 Nov;85(22):8742-6. doi: 10.1073/pnas.85.22.8742.
Purified and reconstituted sodium channels from rat brain have been photoaffinity labeled with a photoactivable derivative of the alpha-scorpion toxin V from Leiurus quinquestriatus (LqTx). A battery of sequence-specific antibodies has been used to determine which of the peptides produced by chemical and enzymatic cleavage of the photolabeled sodium-channel alpha subunit contain covalently attached LqTx. Nearly all of the covalently attached LqTx is found within homologous domain I. Two site-directed antisera, which recognize residues 317 to 335 and residues 382 to 400, respectively, specifically immunoprecipitate a 14-kDa peptide produced by CNBr digestion to which LqTx is covalently attached. It is proposed that a portion of the receptor site for alpha-scorpion toxins is formed by peptide segment(s) between amino acid residues 335 and 378 which is located in an extracellular loop between transmembrane helices S5 and S6 of homologous domain I of the sodium channel alpha subunit.
从大鼠脑中纯化并重组的钠通道已用来自以色列金蝎(Leiurus quinquestriatus)的α-蝎毒素V的光活性衍生物进行了光亲和标记。一系列序列特异性抗体已被用于确定通过对光标记的钠通道α亚基进行化学和酶切产生的哪些肽含有共价连接的LqTx。几乎所有共价连接的LqTx都位于同源结构域I内。两种位点特异性抗血清,分别识别第317至335位残基和第382至400位残基,特异性免疫沉淀由CNBr消化产生的一种14 kDa肽,LqTx共价连接于此肽。有人提出,α-蝎毒素的部分受体位点是由位于钠通道α亚基同源结构域I的跨膜螺旋S5和S6之间的细胞外环中的氨基酸残基335和378之间的肽段形成的。