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首页> 外文期刊>Developmental cell >Profilin Interaction with Actin Filament Barbed End Controls Dynamic Instability, Capping, Branching, and Motility
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Profilin Interaction with Actin Filament Barbed End Controls Dynamic Instability, Capping, Branching, and Motility

机译:Profilin与肌动蛋白丝带刺末端的相互作用可控制动态不稳定性,封端,分支和运动

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摘要

Cell motility and actin homeostasis depend on the control of polarized growth of actin filaments. Profilin, an abundant regulator of actin dynamics, supports filament assembly at barbed ends by binding G-actin. Here, we demonstrate how, by binding and destabilizing filament barbed ends at physiological concentrations, profilin also controls motility, cell migration, and actin homeostasis. Profilin enhances filament length fluctuations. Profilin competes with Capping Protein at barbed ends, which generates a lower amount of profilin-actin than expected if barbed ends were tightly capped. Profilin competes with barbed end polymerases, such as formins and VopF, and inhibits filament branching by WASP-Arp2/3 complex by competition for filament barbed ends, accounting for its as-yet-unknown effects on motility and metastatic cell migration observed in this concentration range. In conclusion, profilin is a major coordinator of polarized growth of actin filaments, controlled by competition between barbed end cappers, trackers, destabilizers, and filament branching machineries.
机译:细胞运动性和肌动蛋白稳态取决于肌动蛋白丝极化生长的控制。 Profilin是肌动蛋白动力学的丰富调节剂,通过结合G-肌动蛋白来支持带刺末端的细丝组装。在这里,我们展示了如何通过在生理浓度下结合和破坏带刺刺丝的末端来稳定它们,profilin还能控制运动性,细胞迁移和肌动蛋白稳态。脯氨酸蛋白增加了丝的长度波动。 Profilin在带刺的末端与Capping Protein竞争,如果将带刺的末端盖紧,则Profilin产生的Profilin-actin量将少于预期。脯氨酸蛋白与带刺的末端聚合酶(如福尔马林和VopF)竞争,并通过竞争带刺的带刺末端来抑制WASP-Arp2 / 3复合物的细丝分支,这是在此浓度下观察到的其对运动性和转移性细胞迁移的未知作用范围。总之,profilin是肌动蛋白丝极化增长的主要协调者,受刺端帽,跟踪仪,去稳定剂和细丝分支机构之间的竞争控制。

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