Pharmacology, Saitama Medical University, 21-7 Wakita-honcho, Kawagoe, Saitama, Japan.
Prog Biophys Mol Biol. 2011 May;105(3):129-33. doi: 10.1016/j.pbiomolbio.2010.12.002. Epub 2010 Dec 14.
The achievements of Natori and Ebashi, which greatly contributed to the progress in studies of excitation-contraction coupling, were reviewed. Natori succeeded in removing the cell membrane of an isolated fiber of skeletal muscle to prepare a skinned fiber, which still responded to an electrical stimulation with propagated contraction. Skinned fibers showed elastic extensibility beyond the elastic limit of intact muscle fibers. Based on this elasticity Natori predicted the presence of an elastic components, later found as connectin. Skinned fibers, an excellent experimental system, contributed greatly to the progress in subsequent studies. Ebashi showed that the essential principle of the relaxing factor was not the ATP-regenerating enzymes as generally thought, but a particulate fraction with MgATPase. Then he clearly showed that a minute amount of Ca(2+) is necessary for the contractile reaction of actomyosin, and that the relaxing factor strongly accumulates Ca(2+) in the presence of ATP and causes relaxation by the removal of Ca(2+). He further discovered that the Ca(2+)-induced regulation of the contractile reaction of the myosin-actin system requires the presence of tropomyosin and a new protein, troponin. Troponin binds to a specific site on tropomyosin, which in turn binds to actin in the thin filament. Troponin is the Ca(2+)-receptive protein, and changes in troponin molecules upon Ca(2+) binding is transmitted to actin through tropomyosin to regulate the actin-myosin interaction. Through these findings, the excitation was connected by Ca(2+) with the contraction.
回顾了 Natori 和 Ebashi 的成就,他们为兴奋-收缩偶联研究的进展做出了巨大贡献。Natori 成功地去除了分离的骨骼肌纤维的细胞膜,制备了一种仍能对电刺激产生传播收缩的去膜纤维。去膜纤维表现出超出完整肌纤维弹性极限的弹性伸展性。基于这种弹性,Natori 预测存在一种弹性成分,后来被发现为连接蛋白。去膜纤维是一种极好的实验系统,为随后的研究进展做出了巨大贡献。Ebashi 表明,松弛因子的基本原理不是普遍认为的 ATP 再生酶,而是具有 MgATPase 的颗粒部分。然后,他清楚地表明,肌球蛋白-肌动蛋白的收缩反应只需要少量的 Ca(2+),并且在存在 ATP 的情况下,松弛因子会强烈地积累 Ca(2+),从而通过去除 Ca(2+) 引起松弛。他进一步发现,钙调蛋白诱导的肌球蛋白-肌动蛋白系统的收缩反应调节需要原肌球蛋白和一种新的蛋白质,肌钙蛋白的存在。肌钙蛋白结合到原肌球蛋白上的特定位点,原肌球蛋白又结合到细肌丝中的肌动蛋白上。肌钙蛋白是 Ca(2+) 受体蛋白,Ca(2+) 结合后肌钙蛋白分子的变化通过原肌球蛋白传递到肌动蛋白,从而调节肌动蛋白-肌球蛋白的相互作用。通过这些发现,兴奋通过 Ca(2+) 与收缩相连接。