INHIBITION OF THE PLASMA-MEMBRANE H+-ATPASE FROM DUNALIELLA-ADIDOPHILA BY OMEPRAZOLE

被引:6
|
作者
SEKLER, I
REMIS, D
GIMMLER, H
PICK, U
机构
[1] WEIZMANN INST SCI, DEPT BIOCHEM, IL-76100 REHOVOT, ISRAEL
[2] UNIV WURZBURG, LEHRSTUHL BOT 1, W-8700 WURZBURG, GERMANY
关键词
OMEPRAZOLE; ATPASE; H+-; (D-ACIDOPHILA);
D O I
10.1016/0005-2728(93)90088-W
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
The acid-activated sulfhydryl reagent omeprazole inhibits light-induced H+ secretion at pH 1 in cells of the halotolerant alga Dunaliella acidophila. Plasma-membrane vesicles, prepared from omeprazole-treated cells, have impaired vanadate-sensitive ATPase and ATP-induced H+ uptake activities. Omeprazole inhibits ATPase activity also in isolated plasma-membrane vesicles. The inhibition is enhanced at acidic pH and can be prevented by protonophores indicating that it is promoted; by internal acidification of the vesicles. Mercaptoethanol partially reverses omeprazole inhibition. ADP does not afford protection against omeprazole but it does protect against inhibition by N-ethylmaleimide, indicating that these reagents modify different sulfhydryl groups. It is suggested that omeprazole blocks SH groups of the D. acidophila plasma-membrane H+-ATPase, which face the outer side of the cell.
引用
收藏
页码:88 / 92
页数:5
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