Microtubule dynamics: an interplay of biochemistry and mechanics

被引:370
作者
Brouhard, Gary J. [1 ]
Rice, Luke M. [2 ]
机构
[1] McGill Univ, Dept Biol, Montreal, PQ, Canada
[2] Univ Texas Southwestern, Dept Biophys, Dallas, TX 75390 USA
基金
加拿大健康研究院; 美国国家科学基金会; 加拿大自然科学与工程研究理事会; 美国国家卫生研究院;
关键词
ALPHA-BETA-TUBULIN; PLUS-END-TRACKING; KINESIN-RELATED PROTEIN; PROMOTES MICROTUBULE; DOUBLECORTIN RECOGNIZES; NUCLEATING ACTIVITY; STRUCTURAL MODEL; BUDDING YEAST; BINDING-SITE; SELF-REPAIR;
D O I
10.1038/s41580-018-0009-y
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Microtubules are dynamic polymers of alpha beta-tubulin that are essential for intracellular organization, organelle trafficking and chromosome segregation. Microtubule growth and shrinkage occur via addition and loss of alpha beta-tubulin subunits, which are biochemical processes. Dynamic microtubules can also engage in mechanical processes, such as exerting forces by pushing or pulling against a load. Recent advances at the intersection of biochemistry and mechanics have revealed the existence of multiple conformations of alpha beta-tubulin subunits and their central role in dictating the mechanisms of microtubule dynamics and force generation. It has become apparent that microtubule-associated proteins (MAPs) selectively target specific tubulin conformations to regulate microtubule dynamics, and mechanical forces can also influence microtubule dynamics by altering the balance of tubulin conformations. Importantly, the conformational states of tubulin dimers are likely to be coupled throughout the lattice: the conformation of one dimer can influence the conformation of its nearest neighbours, and this effect can propagate over longer distances. This coupling provides a long-range mechanism by which MAPs and forces can modulate microtubule growth and shrinkage. These findings provide evidence that the interplay between biochemistry and mechanics is essential for the cellular functions of microtubules.
引用
收藏
页码:451 / 463
页数:13
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