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首页> 外文期刊>Journal of biomedicine & biotechnology >Mechanism of Catch Force: Tethering of Thick and Thin Filaments by Twitchin
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Mechanism of Catch Force: Tethering of Thick and Thin Filaments by Twitchin

机译:捕获力的机制:Twitchin束缚细丝和细丝

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摘要

Catch is a mechanical state occurring in some invertebrate smooth muscles characterized by high force maintenance and resistance to stretch during extremely slow relaxation. During catch, intracellular calcium is near basal concentration and myosin crossbridge cyctng rate is extremely slow. Catch force is relaxed by a protein kinase A-mediated phosphorylation of sites near the N- and C- temini of the minititin twitchin (approx526 kDa). Some catch force maintenance car also occur together with cycling myosin crossbridges at submaximal calcium concentrations, but not when the muscle is maximally activated. Additionally, the link responsible for catch can adjust during shortening of submaximally activated muscles and maintain catch force at the new shorter length. Twitchin binds to both thick and thin filaments, and the thin filament binding shown by both the N- and Cterminal portions of twitchin is decreased by phosphorylation of the sites that regulate catch. The data suggest that the twitchin molecule itself is the catch force bearing tether between thick and thin filaments. We present a model for the regulation of catch in which the twitchin tether can be displaced from thin filaments by both (a) the phosphorylation of twitchin and (b) the attachment of high force myosin crossbridges.
机译:atch抓是一种机械状态,发生在一些无脊椎动物的平滑肌中,其特征在于保持极高的力量并在极慢的放松过程中抵抗拉伸。在捕获过程中,细胞内钙接近基础浓度,而肌球蛋白跨桥循环速率极慢。捕获力通过蛋白激酶A介导的小titintwitchin的N-末端和C-末端的位点(约526 kDa)的磷酸化而放松。一些捕捉力维持车也会在钙浓度低于最大浓度的情况下与循环肌球蛋白横桥同时出现,但不会在肌肉被最大程度地激活时发生。此外,负责捕捉的连杆可以在缩短次最大激活的肌肉期间进行调节,并在新的较短长度上保持捕捉力。 Twitchin既与粗细丝结合,又与细丝结合,并且通过调节捕获物的位点的磷酸化,Twitchin的N端和C端部分都显示出细丝结合。数据表明,twitchin分子本身就是粗​​细丝之间的束缚力。我们提出了一种调节捕获的模型,在该模型中,(a)链球菌素的磷酸化和(b)附着力强的肌球蛋白横桥均可将链球菌素的系链从细丝上移开。

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