首页> 美国卫生研究院文献>The Journal of Biophysical and Biochemical Cytology >Direct electron microscopic visualization of barbed end capping and filament cutting by intestinal microvillar 95-kdalton protein (villin): a new actin assembly assay using the limulus acrosomal process
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Direct electron microscopic visualization of barbed end capping and filament cutting by intestinal microvillar 95-kdalton protein (villin): a new actin assembly assay using the limulus acrosomal process

机译:肠微绒毛95-kdalton蛋白(villin)的带刺端盖和细丝切割的直接电子显微镜可视化:一种使用顶体过程的新型肌动蛋白组装测定法

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摘要

We have re-examined the Ca(++)-dependent interaction of an intestinal microvillar 95- kdalton protein (MV-95K) and actin using the isolated acrosomal process bundles from limulus sperm. Making use of the processes as nuclei for assembling actin filaments, we quantitatively and qualitatively examined MV-95K’s effect on filament assembly and on F- actin, both in the presence and in the absence of Ca(++). The acrosomal processes are particularly advantageous for this approach because they nucleate large numbers of filaments, they are extremely stable, and their morphology can be used to determine the polarity of any nucleated filaments. When filament nucleation was initiated in the presence of MV-95K and the absence of Ca(++), there was biased filament assembly from the bundle ends. The calculated elongation rates from both the barbed and pointed filament ends were virtually indistinguishable from control preparations. In the presence of Ca(++), MV-95K completely inhibited filament assembly from the barbed filament end without affecting the initial rate of assembly from the pointed filament end. The inhibition of assembly results from MV-95K binding to and capping the barbed filament end, thereby preventing monomer addition. This indicates that, while MV-95K is a potent nucleator of actin assembly, it is also a potent inhibitor of actin filament elongation. To examine the effects of MV-95K on F-actin in the presence of Ca(++), we developed an assay where MV-95K is added to filaments previously assembled from acrosomal processes without causing filament breakage during mixing. These results clearly demonstrated that rapid filament shortening by MV-95K results through a mechanism of disrupting intrafilament monomer-monomer interactions. Finally, we show that tropomyosin-containing actin filaments are insensitive to cutting, but not to capping, by MV-95K in the presence of Ca(++).
机译:我们已经重新检查了Ca(++)依赖性的肠道微绒毛95-kdalton蛋白(MV-95K)和肌动蛋白,使用了从精中分离的顶体过程束。利用该过程作为组装肌动蛋白丝的核心,我们定量和定性地研究了有无Ca(++)情况下MV-95K对肌动蛋白丝和F-肌动蛋白的影响。顶体过程对该方法特别有利,因为它们使大量细丝成核,非常稳定,并且它们的形态可用于确定任何成核细丝的极性。当在MV-95K存在且Ca(++)不存在的情况下开始细丝成核时,从束末端出现细丝组件。从带刺的和有尖的长丝末端计算出的伸长率实际上与对照制剂没有区别。在存在Ca(++)的情况下,MV-95K完全抑制了从倒刺的长丝末端开始的长丝组装,而不会影响从尖的长丝末端开始的初始组装速率。组装的抑制是由于MV-95K结合并覆盖了带刺的长丝末端,从而防止了单体的添加。这表明,虽然MV-95K是肌动蛋白装配的有效成核剂,但它还是肌动蛋白丝伸长的有效抑制剂。为了检查在Ca(++)存在下MV-95K对F-肌动蛋白的影响,我们开发了一种测定方法,其中将MV-95K添加到先前由顶体过程组装而成的细丝中,而不会在混合过程中造成细丝断裂。这些结果清楚地表明,通过破坏丝内单体-单体相互作用的机理,MV-95K导致了短丝的快速缩短。最后,我们显示了含有原肌球蛋白的肌动蛋白丝对在Ca(++)存在下通过MV-95K切割不敏感,但对加帽不敏感。

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