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一种参与骨骼肌兴奋-收缩偶联的鸟嘌呤核苷酸结合蛋白?

Is a guanine nucleotide-binding protein involved in excitation-contraction coupling in skeletal muscle?

作者信息

Di Virgilio F, Salviati G, Pozzan T, Volpe P

出版信息

EMBO J. 1986 Feb;5(2):259-62. doi: 10.1002/j.1460-2075.1986.tb04207.x.

Abstract

Plasma membrane depolarization causes skeletal muscle contraction by triggering Ca2+ release from an intracellular membrane network, the sarcoplasmic reticulum. A specialized portion of the sarcoplasmic reticulum, the terminal cisternae, is junctionally associated with sarcolemmal invaginations called the transverse tubules, but the mechanism by which the action potential at the level of the transverse tubules is coupled to Ca2+ release from the terminal cisternae is still mysterious. Here we show that: (i) GTP gamma S, a non-hydrolyzable analog of GTP, elicits isometric force development in skinned muscle fibre; (ii) GTP gamma S is unable to release CA2+ from isolated sarcoplasmic reticulum fractions; (iii) the threshold for tension development is shifted to higher GTP gamma S concentrations by pre-incubation with pertussis toxin. These results suggest that a GTP-binding protein is involved in coupling the action potential of transverse tubules to Ca2+ release from the terminal cisternae.

摘要

质膜去极化通过触发细胞内膜网络(肌浆网)释放Ca2+来引起骨骼肌收缩。肌浆网的一个特殊部分,即终池,与称为横小管的肌膜内陷在连接上相关联,但横小管水平的动作电位与终池Ca2+释放相偶联的机制仍然不明。在此我们表明:(i)GTPγS,一种不可水解的GTP类似物,在去皮肌纤维中引发等长力发展;(ii)GTPγS不能从分离的肌浆网组分中释放Ca2+;(iii)通过用百日咳毒素预孵育,张力发展的阈值向更高的GTPγS浓度偏移。这些结果表明,一种GTP结合蛋白参与了横小管动作电位与终池Ca2+释放的偶联。

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