van der Meulen J A, Emerson D M, Grinstein S
Biochim Biophys Acta. 1981 May 20;643(3):601-15. doi: 10.1016/0005-2736(81)90356-4.
We have tried to define which proteins of chromaffin cell plasma membranes are facing the cytoplasm by surface labelling a selectively oriented membrane preparation. Viable chromaffin cells were isolated by collagenase treatment of bovine adrenals. Plasma membranes from these cells were isolated on polycationic beads by the method of Jacobson and Branton (Jacobson, B.S. and Branton, D. (1977) Science 195, 302--304). The purity and orientation of the membranes were defined by biochemical and morphological criteria. The membranes, with their external side apposed to the bead surface, were enriched about 10-fold with respect to a whole cell homogenate, and contained only small amounts of contaminating organelles. Surface specific iodination of membranes on beads with 1,3,4,6-tetrachloro-3 alpha, 6 alpha-diphenylglycoluril (Iodogen), followed by polyacrylamide gel electrophoresis, allowed the identification of cytoplasmically exposed proteins. A different pattern was observed when intact cells were labelled prior to membrane isolation. The advantages and possible uses of this immobilized membrane preparation are discussed.
我们试图通过对选择性取向的膜制剂进行表面标记,来确定嗜铬细胞质膜中哪些蛋白质面向细胞质。通过用胶原酶处理牛肾上腺来分离活的嗜铬细胞。采用雅各布森和布兰顿的方法(雅各布森,B.S.和布兰顿,D.(1977年)《科学》195卷,302 - 304页),在聚阳离子珠上分离这些细胞的质膜。通过生化和形态学标准来确定膜的纯度和取向。膜的外侧与珠表面相对,相对于全细胞匀浆,其富集了约10倍,并且仅含有少量的污染细胞器。用1,3,4,6 - 四氯 - 3α,6α - 二苯基甘脲(碘甘脲)对珠上的膜进行表面特异性碘化,然后进行聚丙烯酰胺凝胶电泳,从而能够鉴定面向细胞质的蛋白质。在膜分离之前对完整细胞进行标记时,观察到了不同的模式。本文讨论了这种固定化膜制剂的优点和可能的用途。