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肌动蛋白调节管状膜的形状和力学特性。

Actin modulates shape and mechanics of tubular membranes.

作者信息

Allard A, Bouzid M, Betz T, Simon C, Abou-Ghali M, Lemière J, Valentino F, Manzi J, Brochard-Wyart F, Guevorkian K, Plastino J, Lenz M, Campillo C, Sykes C

机构信息

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, Paris, France.

LAMBE, Université Évry Val d'Essonne, CNRS, CEA, Université Paris-Saclay, Évry, France.

出版信息

Sci Adv. 2020 Apr 22;6(17):eaaz3050. doi: 10.1126/sciadv.aaz3050. eCollection 2020 Apr.

Abstract

The actin cytoskeleton shapes cells and also organizes internal membranous compartments. In particular, it interacts with membranes for intracellular transport of material in mammalian cells, yeast, or plant cells. Tubular membrane intermediates, pulled along microtubule tracks, are formed during this process and destabilize into vesicles. While the role of actin in tubule destabilization through scission is suggested, literature also provides examples of actin-mediated stabilization of membranous structures. To directly address this apparent contradiction, we mimic the geometry of tubular intermediates with preformed membrane tubes. The growth of an actin sleeve at the tube surface is monitored spatiotemporally. Depending on network cohesiveness, actin is able to entirely stabilize or locally maintain membrane tubes under pulling. On a single tube, thicker portions correlate with the presence of actin. These structures relax over several minutes and may provide enough time and curvature geometries for other proteins to act on tube stability.

摘要

肌动蛋白细胞骨架塑造细胞形态,并组织内部膜性区室。特别是,它在哺乳动物细胞、酵母或植物细胞中与膜相互作用,以进行细胞内物质运输。在此过程中,沿着微管轨道被拉动的管状膜中间体形成,并不稳定地变成囊泡。虽然有研究表明肌动蛋白在通过切割使微管不稳定中发挥作用,但文献中也提供了肌动蛋白介导膜结构稳定的例子。为了直接解决这一明显的矛盾,我们用预先形成的膜管模拟管状中间体的几何形状。在管表面时空监测肌动蛋白套的生长。根据网络凝聚力,肌动蛋白能够在拉动下完全稳定或局部维持膜管。在单个管子上,较厚的部分与肌动蛋白的存在相关。这些结构在几分钟内松弛,可能为其他蛋白质作用于管的稳定性提供足够的时间和曲率几何形状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1de0/7176416/34edbab81604/aaz3050-F1.jpg

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