St John P A, Froehner S C, Goodenough D A, Cohen J B
J Cell Biol. 1982 Feb;92(2):333-42. doi: 10.1083/jcb.92.2.333.
Experiments were conducted to examine the topographic arrangement of the polypeptides of the acetylcholine receptor (AcChR) and the nonreceptor Mr 43,000 protein in postsynaptic membranes isolated from Torpedo electric organ. When examined by electron microscopy, greater than 85% of vesicles were not permeable to ferritin or lactoperoxidase (LPO). Exposure to saponin was identified as a suitable procedure to permeabilize the vesicles to macromolecules with minimal alteration of vesicle size or ultrastructure. The sidedness of vesicles was examined morphologically and biochemically. Comparison of the distribution of intramembrane particles on freeze-fractured vesicles and the distribution found in situ indicated that greater than 85% of the vesicles were extracellular-side out. Vesicles labeled with alpha-bungarotoxin (alpha-Bgtx) were reacted with antibodies against alpha-BgTx or against purified AcChR of Torpedo. Bound antibodies were detected by the use of ferritin-conjugated goat anti-rabbit antibody and were located on the outside of greater than 99% of labeled vesicles. Similar results were obtained for normal vesicles or vesicles exposed to saponin. Quantification of the amount of [3H]-alpha-BgTx bound to vesicles before and after they were made permeable with saponin indicated that less than 5% of alpha-BgTx binding sites were cryptic in normal vesicles. It was concluded that greater than 95% of postsynaptic membranes were oriented extracellular-side out. LPO-catalyzed radioiodinations were performed on normal and saponin-treated vesicles and on vesicles from which the Mr (relative molecular mass) 43,000 protein had been removed by alkaline extraction. In normal vesicles, polypeptides of the AcChR were iodinated while the Mr 43,000 protein was not. In vesicles made permeable with saponin, the pattern of labeling of AcChR polypeptides was unchanged, but the Mr 43,000 protein was heavily iodinated. The relative iodination of AcChR polypeptides was unchanged in membranes equilibrated with agonist or with alpha-BgTx or after alkaline-extraction. It was concluded that the Mr 43,000 protein is present on the intracellular surface of the postsynaptic membrane and that AcChR polypeptides are exposed on the extracellular surface.
进行了实验,以研究从电鳐电器官分离的突触后膜中乙酰胆碱受体(AcChR)和分子量为43,000的非受体蛋白的多肽的拓扑排列。通过电子显微镜检查时,超过85%的囊泡对铁蛋白或乳过氧化物酶(LPO)不可渗透。已确定用皂角苷处理是使囊泡对大分子通透的合适方法,且对囊泡大小或超微结构的改变最小。从形态学和生物化学方面检查了囊泡的内外侧。比较冷冻断裂囊泡上膜内颗粒的分布与原位发现的分布表明,超过85%的囊泡外侧为细胞外侧。用α-银环蛇毒素(α-Bgtx)标记的囊泡与抗α-BgTx抗体或抗电鳐纯化AcChR的抗体反应。通过使用铁蛋白偶联的山羊抗兔抗体检测结合的抗体,发现其位于超过99%的标记囊泡的外侧。正常囊泡或经皂角苷处理的囊泡也得到了类似结果。对用皂角苷使其通透前后与囊泡结合的[3H]-α-BgTx量进行定量分析表明,正常囊泡中不到5%的α-BgTx结合位点是隐蔽的。得出的结论是,超过95%的突触后膜外侧为细胞外侧。对正常和经皂角苷处理的囊泡以及经碱性提取去除了分子量43,000蛋白的囊泡进行了LPO催化的放射性碘化。在正常囊泡中,AcChR的多肽被碘化,而分子量43,000的蛋白未被碘化。在用皂角苷使其通透的囊泡中,AcChR多肽的标记模式未改变,但分子量43,000的蛋白被大量碘化。在用激动剂或α-BgTx平衡的膜中或碱性提取后,AcChR多肽的相对碘化程度未改变。得出的结论是,分子量43,000的蛋白存在于突触后膜的细胞内表面,而AcChR多肽暴露于细胞外表面。