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肌肉收缩的一种新范式。

A new paradigm for muscle contraction.

作者信息

Herzog Walter, Powers Krysta, Johnston Kaleena, Duvall Mike

机构信息

Faculty of Kinesiology, Engineering, Medicine and Veterinary Medicine, University of Calgary Calgary, AB, Canada.

出版信息

Front Physiol. 2015 Jun 10;6:174. doi: 10.3389/fphys.2015.00174. eCollection 2015.

Abstract

For the past 60 years, muscle contraction had been thought to be governed exclusively by the contractile filaments, actin, and myosin. This thinking explained most observations for concentric and isometric, but not for eccentric muscle contractions. Just over a decade ago, we discovered that eccentric contractions were associated with a force that could not be assigned to actin and myosin, but was at least in part associated with the filamentous protein titin. Titin was found to bind calcium upon activation, thereby increasing its structural stability, and thus its stiffness and force. Furthermore, there is increasing evidence that the proximal part of titin binds to actin in an activation- and force-dependent manner, thereby shortening its free length, thus increasing its stiffness and force. Therefore, we propose that muscle contraction involves three filaments, actin, myosin and titin, and that titin regulates force by binding calcium and by shortening its spring length by binding to actin.

摘要

在过去的60年里,人们一直认为肌肉收缩完全由收缩性细丝肌动蛋白和肌球蛋白控制。这种观点解释了大多数向心收缩和等长收缩的观察结果,但无法解释离心肌肉收缩。就在十多年前,我们发现离心收缩与一种无法归因于肌动蛋白和肌球蛋白的力有关,但至少部分与丝状蛋白肌联蛋白有关。研究发现,肌联蛋白在激活时会结合钙,从而增加其结构稳定性,进而增加其刚度和力量。此外,越来越多的证据表明,肌联蛋白的近端部分以一种依赖激活和力的方式与肌动蛋白结合,从而缩短其自由长度,进而增加其刚度和力量。因此,我们提出肌肉收缩涉及三种细丝,即肌动蛋白、肌球蛋白和肌联蛋白,并且肌联蛋白通过结合钙以及通过与肌动蛋白结合来缩短其弹簧长度来调节力量。

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