Department of Physics, Lomonosov Moscow State University, Moscow, Russia.
Center for Theoretical Problems of Physicochemical Pharmacology, Russian Academy of Sciences, Moscow, Russia.
Nat Rev Mol Cell Biol. 2021 Dec;22(12):777-795. doi: 10.1038/s41580-021-00399-x. Epub 2021 Aug 18.
Microtubule dynamics and their control are essential for the normal function and division of all eukaryotic cells. This plethora of functions is, in large part, supported by dynamic microtubule tips, which can bind to various intracellular targets, generate mechanical forces and couple with actin microfilaments. Here, we review progress in the understanding of microtubule assembly and dynamics, focusing on new information about the structure of microtubule tips. First, we discuss evidence for the widely accepted GTP cap model of microtubule dynamics. Next, we address microtubule dynamic instability in the context of structural information about assembly intermediates at microtubule tips. Three currently discussed models of microtubule assembly and dynamics are reviewed. These are considered in the context of established facts and recent data, which suggest that some long-held views must be re-evaluated. Finally, we review structural observations about the tips of microtubules in cells and describe their implications for understanding the mechanisms of microtubule regulation by associated proteins, by mechanical forces and by microtubule-targeting drugs, prominently including cancer chemotherapeutics.
微管动力学及其调控对于所有真核细胞的正常功能和分裂至关重要。这种众多的功能在很大程度上是由动态微管尖端支持的,它可以与各种细胞内靶标结合,产生机械力并与肌动蛋白微丝偶联。在这里,我们回顾了对微管组装和动力学的理解的进展,重点介绍了关于微管尖端结构的新信息。首先,我们讨论了广泛接受的微管动力学 GTP 帽模型的证据。接下来,我们在微管尖端组装中间体的结构信息的背景下讨论微管动态不稳定性。我们回顾了三种当前讨论的微管组装和动力学模型。在既定事实和最近数据的背景下考虑这些模型,这表明一些长期存在的观点必须重新评估。最后,我们回顾了关于细胞中微管尖端的结构观察,并描述了它们对理解相关蛋白、机械力和微管靶向药物(尤其是癌症化疗药物)调节微管机制的影响。