Effects of hydroxyl radical and sulfhydryl reagents on the open probability of the purified cardiac ryanodine receptor channel incorporated into planar lipid bilayers

被引:79
作者
Anzai, K [1 ]
Ogawa, K
Kuniyasu, A
Ozawa, T
Yamamoto, H
Nakayama, H
机构
[1] Natl Inst Radiol Sci, Bioregulat Res Grp, Chiba 260, Japan
[2] Kanagawa Univ, Dept Appl Biosci, Fac Sci, Yokohama, Kanagawa, Japan
[3] Kumamoto Univ, Fac Pharmaceut Sci, Kumamoto 860, Japan
关键词
D O I
10.1006/bbrc.1998.9244
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
We examined the effects of hydroxyl radical on the ion permeability of the ryanodine receptor, a calcium releasing channel of sarcoplasmic reticulum. The cardiac ryanodine receptor, purified from pig heart, was reconstituted to proteoliposomes and then incorporated into a planar bilayer membrane. A single channel activity with a conductance of 724 pS in 900/200 mM (cis/trans) KCl and an ion selectivity of P-K:P-CI = 1:0.08 was observed. These characteristics are similar to those observed by the incorporation of the channel through sarcoplasmic reticulum vesicles. Hydroxyl radicals chemically generated by the reaction of H2O2 and Cu(ethylenediamine)(2) at the cis compartment increased the open probability of the channel. Treatment with SH oxidizing reagents from the cis compartment also increased the open probability, and dithiothreitol, a SH reducing agent, reversed the effect. These findings suggest that hydroxyl radicals react with some SH groups of the ryanodine receptor and increase the Ca2+ release from sarcoplasmic reticulum through the ryanodine receptor. (C) 1998 Academic Press.
引用
收藏
页码:938 / 942
页数:5
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