NEW METHOD OF PREPARING CA2+-ATPASE FROM SARCOPLASMIC-RETICULUM - EXTRACTION WITH OCTYLGLUCOSIDE

被引:36
作者
BANERJEE, R [1 ]
EPSTEIN, M [1 ]
KANDRACH, M [1 ]
ZIMNIAK, P [1 ]
RACKER, E [1 ]
机构
[1] CORNELL UNIV,BIOCHEM SECT,ITHACA,NY 14853
来源
MEMBRANE BIOCHEMISTRY | 1979年 / 2卷 / 3-4期
关键词
D O I
10.3109/09687687909063868
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A fast method for preparing Ca2+-ATPase from rabbit muscle sarcoplasmic reticulum was devised. The method involves extracting extrinsic membrane proteins with the non-ionic detergent octylglucoside at high salt concentration. A Ca2+ ATPase of consistently high specific activity (about 25 μmoles/mg·min) is found in the insoluble residue. The method was optimized with respect to the concentrations of detergent and salt, pH, and other extraction conditions. By the criteria of the protein pattern in SDS-polyacrylamide gel electrophoresis, dependence of the hydrolytic activity on the presence of Ca2+, and the phosphoprotein formation, the preparation is identical with the Ca2+-ATPase isolated previously by MacLennan [10] and other authors. The main advantages of the new method are its rapidity, its reliability, and the high specific activity of the purified enzyme. © 1979 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted.
引用
收藏
页码:283 / 296
页数:14
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