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棘阿米巴中磷酸化肌球蛋白I亚型的定量与定位

Quantification and localization of phosphorylated myosin I isoforms in Acanthamoeba castellanii.

作者信息

Baines I C, Corigliano-Murphy A, Korn E D

机构信息

Laboratory of Cell Biology, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

J Cell Biol. 1995 Aug;130(3):591-603. doi: 10.1083/jcb.130.3.591.

Abstract

The actin-activated Mg(2+)-ATPase activities of the three myosin I isoforms in Acanthamoeba castellanii are significantly expressed only after phosphorylation of a single site in the myosin I heavy chain. Synthetic phosphorylated and unphosphorylated peptides corresponding to the phosphorylation site sequences, which differ for the three myosin I isoforms, were used to raise isoform-specific antibodies that recognized only the phosphorylated myosin I or the total myosin I isoform (phosphorylated and unphosphorylated), respectively. With these antisera, the amounts of total and phosphorylated isoform were quantified, the phosphomyosin I isoforms localized, and the compartmental distribution of the phosphomyosin isoforms determined. Myosin IA, which was almost entirely in the actin-rich cortex, was 70-100% phosphorylated and particularly enriched under phagocytic cups. Myosins IB and IC were predominantly associated with plasma membranes and large vacuole membranes, where they were only 10-20% phosphorylated, whereas cytoplasmic myosins IB and IC, like cytoplasmic myosin IA, were mostly phosphorylated (60-100%). Moreover, phosphomyosin IB was concentrated in actively motile regions of the plasma membrane. More than 20-fold more phosphomyosin IC and 10-fold more F-actin were associated with the membranes of contracting contractile vacuoles (CV) than of filling CVs. As the total amount of CV-associated myosin IC remained constant, it must be phosphorylated at the start of CV contraction. These data extend previous proposals for the specific functions of myosin I isozymes in Acanthamoeba (Baines, I.C., H. Brzeska, and E.D. Korn. 1992. J. Cell Biol. 119: 1193-1203): phosphomyosin IA in phagocytosis, phosphomyosin IB in phagocytosis and pinocytosis, and phosphomyosin IC in contraction of the CV.

摘要

在棘阿米巴中,三种肌球蛋白I同工型的肌动蛋白激活的Mg(2+)-ATP酶活性仅在肌球蛋白I重链中的单个位点磷酸化后才显著表达。与磷酸化位点序列相对应的合成磷酸化和未磷酸化肽段,这三种肌球蛋白I同工型的序列不同,用于产生仅识别磷酸化肌球蛋白I或总肌球蛋白I同工型(磷酸化和未磷酸化)的同工型特异性抗体。利用这些抗血清,对总同工型和磷酸化同工型的量进行了定量,对磷酸化肌球蛋白I同工型进行了定位,并确定了磷酸化肌球蛋白同工型的区室分布。几乎完全位于富含肌动蛋白的皮层中的肌球蛋白IA,磷酸化程度为70-100%,在吞噬杯下尤其富集。肌球蛋白IB和IC主要与质膜和大液泡膜相关,在那里它们的磷酸化程度仅为10-20%,而细胞质中的肌球蛋白IB和IC,与细胞质中的肌球蛋白IA一样,大多被磷酸化(60-100%)。此外,磷酸化肌球蛋白IB集中在质膜的活跃运动区域。与正在收缩的收缩泡(CV)的膜相比,与充盈的CV的膜相关的磷酸化肌球蛋白IC多20倍以上,F-肌动蛋白多10倍。由于与CV相关的肌球蛋白IC的总量保持不变,它一定是在CV收缩开始时被磷酸化的。这些数据扩展了先前关于棘阿米巴中肌球蛋白I同工酶特定功能的提议(Baines, I.C., H. Brzeska, and E.D. Korn. 1992. J. Cell Biol. 119: 1193-1203):吞噬作用中的磷酸化肌球蛋白IA,吞噬作用和胞饮作用中的磷酸化肌球蛋白IB,以及CV收缩中的磷酸化肌球蛋白IC。

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