中心体
微管
微管蛋白
生物
微管形核
细胞生物学
中心粒
高分子拥挤
微管组织中心
生物物理学
生物化学
细胞周期
细胞
高分子
作者
Jeffrey B. Woodruff,Beatriz Ferreira Gomes,Per O. Widlund,Julia Mahamid,Alf Honigmann,Anthony A. Hyman
出处
期刊:Cell
[Elsevier]
日期:2017-06-01
卷期号:169 (6): 1066-1077.e10
被引量:625
标识
DOI:10.1016/j.cell.2017.05.028
摘要
Centrosomes are non-membrane-bound compartments that nucleate microtubule arrays. They consist of nanometer-scale centrioles surrounded by a micron-scale, dynamic assembly of protein called the pericentriolar material (PCM). To study how PCM forms a spherical compartment that nucleates microtubules, we reconstituted PCM-dependent microtubule nucleation in vitro using recombinant C. elegans proteins. We found that macromolecular crowding drives assembly of the key PCM scaffold protein SPD-5 into spherical condensates that morphologically and dynamically resemble in vivo PCM. These SPD-5 condensates recruited the microtubule polymerase ZYG-9 (XMAP215 homolog) and the microtubule-stabilizing protein TPXL-1 (TPX2 homolog). Together, these three proteins concentrated tubulin ∼4-fold over background, which was sufficient to reconstitute nucleation of microtubule asters in vitro. Our results suggest that in vivo PCM is a selective phase that organizes microtubule arrays through localized concentration of tubulin by microtubule effector proteins.
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