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是撒谎还是不撒谎:与肌球蛋白一起超级放松。

To lie or not to lie: Super-relaxing with myosins.

机构信息

Department of Biology, MyoKardia Inc, Brisbane, United States.

Department of Biochemistry, Stanford University School of Medicine, Stanford, United States.

出版信息

Elife. 2021 Feb 10;10:e63703. doi: 10.7554/eLife.63703.

Abstract

Since the discovery of muscle in the 19th century, myosins as molecular motors have been extensively studied. However, in the last decade, a new functional super-relaxed (SRX) state of myosin has been discovered, which has a 10-fold slower ATP turnover rate than the already-known non-actin-bound, disordered relaxed (DRX) state. These two states are in dynamic equilibrium under resting muscle conditions and are thought to be significant contributors to adaptive thermogenesis in skeletal muscle and can act as a reserve pool that may be recruited when there is a sustained demand for increased cardiac muscle power. This report provides an evolutionary perspective of how striated muscle contraction is regulated by modulating this myosin DRX↔SRX state equilibrium. We further discuss this equilibrium with respect to different physiological and pathophysiological perturbations, including insults causing hypertrophic cardiomyopathy, and small-molecule effectors that modulate muscle contractility in diseased pathology.

摘要

自 19 世纪发现肌肉以来,肌球蛋白作为分子马达已经得到了广泛的研究。然而,在过去的十年中,一种新的功能超松弛(SRX)状态的肌球蛋白已经被发现,其 ATP 周转率比已经知道的非肌动蛋白结合的、无序松弛(DRX)状态慢 10 倍。这两种状态在静止肌肉条件下处于动态平衡,并被认为是骨骼肌适应性产热的重要贡献者,并且可以作为储备池,当需要持续增加心肌力量时,可以被招募。本报告提供了一个进化的观点,即通过调节肌球蛋白 DRX↔SRX 状态平衡来调节横纹肌收缩。我们进一步讨论了这种平衡与不同生理和病理生理扰动之间的关系,包括导致肥厚型心肌病的损伤,以及在疾病病理中调节肌肉收缩性的小分子效应物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a62a/7875563/784e48a20b74/elife-63703-fig1.jpg

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