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肌浆网大小电导的单通道钙电流和钡电流

Single-channel calcium and barium currents of large and small conductance from sarcoplasmic reticulum.

作者信息

Smith J S, Coronado R, Meissner G

出版信息

Biophys J. 1986 Nov;50(5):921-8. doi: 10.1016/S0006-3495(86)83533-0.

Abstract

Two types of divalent cation conducting channels from rabbit skeletal muscle sarcoplasmic reticulum (SR) were incorporated into planar lipid bilayers. A high conductance (100 pS in 53 mM trans Ca2+) Ca2+ channel was incorporated from heavy density SR fractions. The 100-pS channel was activated by adenine nucleotides and Ca2+ and inhibited by Mg2+ and ruthenium red. A 10-pS calcium and barium conducting channel could be incorporated into planar lipid bilayers from light, intermediate, and heavy density SR vesicles. 10-pS channel activity in bilayers was not dependent on cis Ca2+ and was only weakly dependent on adenine nucleotides. Ruthenium red at concentrations up to 1 mM had no effect and Mg2+ was only marginally effective in inhibiting macroscopic Ba2+ currents from this channel. Calcium releasing activity in intermediate and heavy density SR fractions was assayed according to a rapid quench protocol and compared with the results obtained in the bilayer. Results from this comparison indicate that the 10-pS channel is probably not involved in rapid Ca2+- and adenine nucleotide-induced Ca2+ release from isolated SR vesicles.

摘要

从兔骨骼肌肌浆网(SR)中提取的两种二价阳离子传导通道被整合到平面脂质双分子层中。从高密度SR组分中整合出一种高电导(在53 mM反式Ca2+中为100 pS)的Ca2+通道。100-pS通道被腺嘌呤核苷酸和Ca2+激活,并被Mg2+和钌红抑制。一种10-pS的钙和钡传导通道可从低密度、中密度和高密度SR囊泡整合到平面脂质双分子层中。双分子层中的10-pS通道活性不依赖于顺式Ca2+,仅微弱依赖于腺嘌呤核苷酸。浓度高达1 mM的钌红没有作用,Mg2+对抑制该通道的宏观Ba2+电流仅有微弱效果。根据快速淬灭方案测定中密度和高密度SR组分中的钙释放活性,并与双分子层中获得的结果进行比较。该比较结果表明,10-pS通道可能不参与从分离的SR囊泡中快速的Ca2+和腺嘌呤核苷酸诱导的Ca2+释放。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd43/1329817/046c96f1bc39/biophysj00173-0151-a.jpg

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