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首页> 外文期刊>Journal of Muscle Research and Cell Motility >Intensity of X-ray reflections from skeletal muscle thin filaments partially occupied with myosin heads: effect of cooperative binding
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Intensity of X-ray reflections from skeletal muscle thin filaments partially occupied with myosin heads: effect of cooperative binding

机译:来自部分被肌球蛋白头部占据的骨骼肌细丝的X射线反射强度:协同结合的作用

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摘要

For quantitative analysis of contractile proteins of muscle by means of X-ray diffraction, it is important to know how the intensities of individual reflections are related to the number of diffracting objects, i.e., the amount of constituent contractile protein in the muscle cell. Here we diffused various amounts of exogenous myosin subfragment-1 (S1) into overstretched skinned skeletal muscle fibers, either in the presence or absence of Ca2+ , and derived the relationship between the S1 content and the intensities of reflections arising from the S1. In theory, the intensities should be proportional to the square of the S1 content (square law). However, the intensity--content relation deviated systematically from the square law as the S1 content was lowered, and it was better described as a linear function at the lower end of the S1 contents (<20% of saturation level). Model calculations show that the way of deviation is explained by the cooperative manner of S1 binding to the regulated thin filament.
机译:为了通过X射线衍射对肌肉的收缩蛋白进行定量分析,重要的是要知道各个反射的强度与衍射物的数量,即肌肉细胞中的收缩蛋白的量如何相关。在这里,我们在有或没有Ca2 +的情况下,将各种数量的外源性肌球蛋白亚片段1(S1)扩散到过度拉伸的皮肤骨骼肌纤维中,得出S1含量与反射强度之间的关系。 S1。理论上,强度应与S1含量的平方成正比(平方律)。但是,随着S1含量的降低,强度与含量的关系系统地偏离平方律,最好将其描述为S1含量下端的线性函数(饱和度<20%)。模型计算表明,S1结合到调节的细丝上的协同方式解释了偏离的方式。

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