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在肌肉收缩过程中,许多横桥同时附着的模型可以解释每消耗一个ATP所产生的细丝运动。

Models in which many cross-bridges attach simultaneously can explain the filament movement per ATP split during muscle contraction.

作者信息

Barclay C J

机构信息

School of Physiotherapy and Exercise Science, Griffith University, Gold Coast Campus, PMB 50 Gold Coast Mail Centre, Queensland, Australia.

出版信息

Int J Biol Macromol. 2003 Sep;32(3-5):139-47. doi: 10.1016/s0141-8130(03)00047-3.

Abstract

Contractile filaments in skeletal muscle are moved by less than 2nm for each ATP used. If just one cross-bridge is attached to each thin filament at any instant then this distance represents the fundamental myosin cross-bridge step size (i.e. the distance one cross-bridge moves a thin filament in one ATP-splitting cycle). However, most contraction models assume many cross-bridges are attached at any instant along each thin filament. The purpose of this study was to establish whether the net filament sliding per ATP used could be explained quantitatively in terms of a cross-bridge model in which multiple cross-bridges are attached along each thin filament. It was found that the relationship between net filament sliding per ATP split and the load against which the muscle shortens is compatible with such a model and furthermore predicts that the cross-bridge step size is between 7.5 and 12.5nm over most of the range of loads. These values were similar for different muscle fibre types.

摘要

骨骼肌中的收缩细丝每消耗一个ATP移动不到2纳米。如果在任何时刻每条细肌丝上仅附着一个横桥,那么这个距离就代表了肌球蛋白横桥的基本步长(即一个横桥在一个ATP水解循环中使细肌丝移动的距离)。然而,大多数收缩模型假设在任何时刻沿着每条细肌丝都附着有许多横桥。本研究的目的是确定每消耗一个ATP时细丝的净滑动是否可以根据一个横桥模型进行定量解释,在该模型中沿着每条细肌丝附着有多个横桥。研究发现,每分解一个ATP时细丝的净滑动与肌肉缩短所对抗的负荷之间的关系与这样一个模型相符,而且进一步预测在大多数负荷范围内横桥步长在7.5至12.5纳米之间。不同肌肉纤维类型的这些值相似。

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