Bloch R J, Resneck W G, O'Neill A, Strong J, Pumplin D W
Department of Physiology, University of Maryland School of Medicine, Baltimore 21201.
J Cell Biol. 1991 Oct;115(2):435-46. doi: 10.1083/jcb.115.2.435.
A 58-kD protein, identified in extracts of postsynaptic membrane from Torpedo electric organ, is enriched at sites where acetylcholine receptors (AChR) are concentrated in vertebrate muscle (Froehner, S. C., A. A. Murnane, M. Tobler, H. B. Peng, and R. Sealock. 1987. J. Cell Biol. 104:1633-1646). We have studied the 58-kD protein in AChR clusters isolated from cultured rat myotubes. Using immunofluorescence microscopy we show that the 58-kD protein is highly enriched at AChR clusters, but is also present in regions of the myotube membrane lacking AChR. Within clusters, the 58-kD protein codistributes with AChR, and is absent from adjacent membrane domains involved in myotube-substrate contact. Semiquantitative fluorescence measurements suggest that molecules of the 58-kD protein and AChR are present in approximately equal numbers. Differential extraction of peripheral membrane proteins from isolated AChR clusters suggests that the 58-kD protein is more tightly bound to cluster membrane than is actin or spectrin, but less tightly bound than the receptor-associated 43-kD protein. When AChR clusters are disrupted either in intact cells or after isolation, the 58-kD protein still codistributes with AChR. Clusters visualized by electron microscopy after immunogold labeling and quick-freeze, deep-etch replication show that, within AChR clusters, the 58-kD protein is sharply confined to AChR-rich domains, where it is present in a network of filaments lying on the cytoplasmic surface of the membrane. Additional actin filaments overlie, and are attached to, this network. Our results suggest that within AChR domains of clusters, the 58-kD protein lies between AChR and the receptor-associated 43-kD protein, and the membrane-skeletal proteins, beta-spectrin, and actin.
在电鳐电器官的突触后膜提取物中鉴定出的一种58-kD蛋白,在脊椎动物肌肉中乙酰胆碱受体(AChR)聚集的部位高度富集(Froehner, S. C., A. A. Murnane, M. Tobler, H. B. Peng, and R. Sealock. 1987. J. Cell Biol. 104:1633 - 1646)。我们研究了从培养的大鼠肌管中分离出的AChR簇中的58-kD蛋白。利用免疫荧光显微镜,我们发现58-kD蛋白在AChR簇中高度富集,但也存在于缺乏AChR的肌管膜区域。在簇内,58-kD蛋白与AChR共分布,而在参与肌管 - 底物接触的相邻膜结构域中不存在。半定量荧光测量表明,58-kD蛋白和AChR分子的数量大致相等。从分离的AChR簇中对外周膜蛋白进行差异提取表明,58-kD蛋白比肌动蛋白或血影蛋白与簇膜的结合更紧密,但比受体相关的43-kD蛋白结合得更松散。当AChR簇在完整细胞中或分离后被破坏时,58-kD蛋白仍与AChR共分布。免疫金标记和快速冷冻、深度蚀刻复制后通过电子显微镜观察到的簇表明,在AChR簇内,58-kD蛋白严格局限于富含AChR的结构域,在那里它存在于位于膜细胞质表面的细丝网络中。额外的肌动蛋白丝覆盖并附着在这个网络上。我们的结果表明,在簇的AChR结构域内,58-kD蛋白位于AChR与受体相关的43-kD蛋白以及膜骨架蛋白β-血影蛋白和肌动蛋白之间。