A novel method of extraction of TnC from skeletal muscle myofibrils

被引:7
作者
Allhouse, LD
Potter, JD
Ashley, CC
机构
[1] Univ Oxford, Physiol Lab, Oxford OX1 3PT, England
[2] Univ Miami, Sch Med, Dept Mol & Cellular Pharmacol, Miami, FL 33101 USA
[3] Friday Harbor Labs, Friday Harbor, WA 98250 USA
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 1999年 / 437卷 / 05期
基金
英国惠康基金;
关键词
calcium; muscle; skeletal; vanadate;
D O I
10.1007/s004240050834
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Incubation of mechanically skinned barnacle myofibrillar bundles in 10 mM orthovanadate (pH 6.6) results in the loss of Ca2+-dependent force generation, which reduces to 0.98+/-0.006% (mean +/- SEM, n=25) of control levels. Analysis of myofibrillar bundles by gel electrophoresis showed that tension loss is primarily due to the extraction of troponin C (TnC) (65.4+/-5.04% mean +/-SEM, n=5). This is a novel finding, since treating cardiac fibres with orthovanadate results in the removal of both TnC and troponin I (TnI) (28). Ca2+ dependence was restored to the myofibrillar bundles following reconstitution with either native isoform of barnacle TnC (BTnC(1): 78.72+/-12.8%, n=9, BTnC(2): 82.73+/-20.3%, n=3). The reversible loss of Ca2+-dependent tension generation following the removal and replacement of TnC indicates that the regulation of contraction in the barnacle is controlled by thin-filament regulatory proteins.
引用
收藏
页码:695 / 701
页数:7
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