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平滑肌重酶解肌球蛋白磷酸化依赖性调节机制

Mechanism of the phosphorylation-dependent regulation of smooth muscle heavy meromyosin.

作者信息

Sellers J R

出版信息

J Biol Chem. 1985 Dec 15;260(29):15815-9.

PMID:2933403
Abstract

Phosphorylation of smooth muscle heavy meromyosin (HMM) has been shown to result in about a 25-fold increase in the steady-state Vmax of the actin-activated MgATPase activity from 0.07 s-1 for unphosphorylated HMM to 1.9 s-1 for phosphorylated HMM. The steady-state MgATPase activity of unphosphorylated HMM in the absence of actin is 0.004 s-1. The true extent of regulation might be even larger since the actin activation of the MgATPase activity of unphosphorylated HMM (from 0.004 to 0.07 s-1 at Vmax) could be arising from a small fraction of modified HMM molecules which are no longer regulated and that truly regulated unphosphorylated HMM molecules are not activated by actin. To test this idea, a "limited turnover" experiment was used to measure the reassociation rate of acto-unphosphorylated HMM following addition of a 2-4-fold molar excess of ATP. The reassociation rate was very slow and was not significantly increased by raising the actin concentration from 10 to 75 microM or by addition of trace phosphorylated HMM. The rate constant was estimated to be about 0.002 s-1, which is in good agreement with the rate of product (both Pi and ADP) release estimated from unphosphorylated HMM alone measured by a gel filtration technique. These two experiments suggest that the rate of product release from unphosphorylated HMM may not be significantly affected by actin and that perhaps the true extent of regulation of HMM by phosphorylation is much greater than that determined by steady-state methods. It also suggests that phosphorylation may operate by increasing the forward rate constant for product release by approximately 1000-fold.

摘要

已表明平滑肌重酶解肌球蛋白(HMM)的磷酸化会导致肌动蛋白激活的MgATP酶活性的稳态Vmax增加约25倍,从未磷酸化HMM的0.07 s-1增加到磷酸化HMM的1.9 s-1。在没有肌动蛋白的情况下,未磷酸化HMM的稳态MgATP酶活性为0.004 s-1。实际的调节程度可能更大,因为未磷酸化HMM的MgATP酶活性的肌动蛋白激活作用(在Vmax时从0.004增加到0.07 s-1)可能来自一小部分不再受调节的修饰HMM分子,而真正受调节的未磷酸化HMM分子不会被肌动蛋白激活。为了验证这一想法,采用了“有限周转”实验来测量添加2 - 4倍摩尔过量ATP后肌动蛋白 - 未磷酸化HMM的重新结合速率。重新结合速率非常缓慢,并且通过将肌动蛋白浓度从10 microM提高到75 microM或添加微量磷酸化HMM,该速率没有显著增加。估计速率常数约为0.002 s-1,这与通过凝胶过滤技术单独测量的未磷酸化HMM估计的产物(Pi和ADP)释放速率非常一致。这两个实验表明,肌动蛋白可能不会显著影响未磷酸化HMM的产物释放速率,并且磷酸化对HMM的实际调节程度可能比稳态方法所确定的要大得多。这也表明磷酸化可能通过将产物释放的正向速率常数提高约1000倍来起作用。

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