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4,4'-二硫代二吡啶引起的离体肌浆网钙释放

Calcium release from isolated sarcoplasmic reticulum due to 4,4'-dithiodipyridine.

作者信息

Nagura S, Kawasaki T, Taguchi T, Kasai M

机构信息

Departmeht of Biophysical Engineering, Faculty of Engineering Science, Osaka University.

出版信息

J Biochem. 1988 Sep;104(3):461-5. doi: 10.1093/oxfordjournals.jbchem.a122490.

Abstract

The effects of SH reagents on Ca2+ release from sarcoplasmic reticulum (SR) vesicles were examined by the tracer method using 45Ca2+. Among the various SH reagents tested, 4,4'-dithiodipyridine (PDS) was found to induce Ca2+ release most specifically from the heavy fraction of SR vesicles. Further, the following results were obtained. (i) PDS bound covalently to proteins in the SR membrane and induced Ca2+ release. (ii) The Ca2+ release was further enhanced by ATP and caffeine, but inhibited by procaine, ruthenium red and various divalent cations. (iii) PDS enhanced the Ca2+ release in the whole range of Ca2+ concentrations tested. (iv) Choline permeability was also enhanced by PDS. Further, the electrical conductance of the Ca2+-induced Ca2+ release channels was studied by incorporating them into lipid bilayers and it was found that PDS increased the probability of opening of the channels. These results suggest that PDS binds to certain SH groups of the Ca2+-induced Ca2+ release channels in the SR membrane and thus induces Ca2+ release.

摘要

利用45Ca2+示踪法研究了巯基(SH)试剂对肌浆网(SR)囊泡Ca2+释放的影响。在所测试的各种SH试剂中,发现4,4'-二硫代二吡啶(PDS)能最特异性地诱导Ca2+从SR囊泡的重组分中释放。此外,还获得了以下结果。(i)PDS与SR膜中的蛋白质共价结合并诱导Ca2+释放。(ii)ATP和咖啡因可进一步增强Ca2+释放,但普鲁卡因、钌红和各种二价阳离子可抑制Ca2+释放。(iii)在整个测试的Ca2+浓度范围内,PDS均增强了Ca2+释放。(iv)PDS还增强了胆碱通透性。此外,通过将Ca2+诱导的Ca2+释放通道整合到脂质双层中,研究了其电导,发现PDS增加了通道开放的概率。这些结果表明,PDS与SR膜中Ca2+诱导的Ca2+释放通道的某些SH基团结合,从而诱导Ca2+释放。

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