Porter S, Froehner S C
J Biol Chem. 1983 Aug 25;258(16):10034-40.
A protein of Mr = 43,000 (43K protein) is a major component of highly purified postsynaptic membranes isolated from Torpedo electric organ. It can be removed from these membranes by alkaline treatment or with 10 mM lithium diiodosalicylate, conditions which extract peripheral membrane proteins without solubilizing the acetylcholine receptor. Two-dimensional polyacrylamide gel electrophoresis of the lithium diiodosalicylate extract shows it to contain several major Mr = 43,000 components of isoelectric points between 7.0 and 8.0 and a minor component of approximately pI 5.6. The pI 5.6 polypeptide co-migrates with skeletal muscle actin on a two-dimensional gel and gives a peptide map pattern very similar to that of actin. The three major spots of pI 7.0-8.0 yield peptide maps which are indistinguishable from one another but quite different from that of actin. The membrane-bound forms of both the basic 43K protein and actin can be iodinated in a lactoperoxidase-catalyzed reaction only if the membrane vesicles are first permeabilized with saponin, a treatment which permits entry of macromolecules to the interior of the vesicles. An immunoblot of a two-dimensional gel shows that a rabbit antiserum made against alkaline extract reacts strongly with the basic 43K protein and to lesser extent with an acidic component of Mr = 55,000 but not with actin. Immunofluorescence studies have shown that this antiserum reacts with the innervated face of Torpedo electrocytes and recognizes a component of rat diaphragm muscle which is highly concentrated at the neuromuscular junction (Froehner, S.C., Gulbrandsen, V., Hyman, C., Jeng, A. Y., Neubig, R. R., and Cohen, J. B. (1981) Proc. Natl. Acad. Sci. U. S. A. 78, 5230-5234). Similar experiments on intact rat muscle indicate that, like the 43K protein of Torpedo postsynaptic membranes, the immunologically related component in mammalian muscle endplates is located on the cytoplasmic side of the postsynaptic membrane.
分子量为43,000的蛋白质(43K蛋白质)是从电鳐电器官中分离出的高度纯化的突触后膜的主要成分。通过碱性处理或用10 mM二碘水杨酸锂可将其从这些膜中去除,在这些条件下可提取外周膜蛋白而不使乙酰胆碱受体溶解。二碘水杨酸锂提取物的二维聚丙烯酰胺凝胶电泳显示,它含有几种主要的分子量为43,000、等电点在7.0至8.0之间的成分以及一种等电点约为5.6的次要成分。在二维凝胶上,等电点为5.6的多肽与骨骼肌肌动蛋白迁移位置相同,并且给出的肽图模式与肌动蛋白非常相似。等电点为7.0 - 8.0的三个主要斑点产生的肽图彼此无法区分,但与肌动蛋白的肽图有很大不同。只有当膜囊泡先用皂素通透处理(这种处理允许大分子进入囊泡内部)后,碱性43K蛋白质和肌动蛋白的膜结合形式才能在乳过氧化物酶催化的反应中被碘化。二维凝胶的免疫印迹显示,针对碱性提取物制备的兔抗血清与碱性43K蛋白质强烈反应,与分子量为55,000的酸性成分反应较弱,但与肌动蛋白不反应。免疫荧光研究表明,这种抗血清与电鳐电细胞的受神经支配面反应,并识别大鼠膈肌中高度集中在神经肌肉接头处的一种成分(弗勒纳,S.C.,古尔布兰德森,V.,海曼,C.,郑,A.Y.,纽比格,R.R.,和科恩,J.B.(1981年)美国国家科学院院刊78,5230 - 5234)。对完整大鼠肌肉进行的类似实验表明,与电鳐突触后膜的43K蛋白质一样,哺乳动物肌肉终板中免疫相关成分位于突触后膜的细胞质一侧。