Ti Shih-Chieh
School of Biomedical Sciences, Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong SAR, China.
Front Cell Dev Biol. 2022 Apr 28;10:861648. doi: 10.3389/fcell.2022.861648. eCollection 2022.
Microtubules are cytoskeletal filaments underlying the morphology and functions of all eukaryotic cells. In higher eukaryotes, the basic building blocks of these non-covalent polymers, ɑ- and β-tubulins, are encoded by expanded tubulin family genes (i.e., isotypes) at distinct loci in the genome. While ɑ/β-tubulin heterodimers have been isolated and examined for more than 50 years, how tubulin isotypes contribute to the microtubule organization and functions that support diverse cellular architectures remains a fundamental question. To address this knowledge gap, reconstitution of microtubules with purified ɑ/β-tubulin proteins has been employed for biochemical and biophysical characterization. These assays have provided mechanistic insights into the regulation of microtubule dynamics, stability, and interactions with other associated proteins. Here we survey the evolving strategies of generating purified ɑ/β-tubulin heterodimers and highlight the advances in tubulin protein biochemistry that shed light on the roles of tubulin isotypes in determining microtubule structures and properties.
微管是所有真核细胞形态和功能的细胞骨架细丝。在高等真核生物中,这些非共价聚合物的基本组成部分α-和β-微管蛋白,由基因组中不同位点的扩展微管蛋白家族基因(即同种型)编码。虽然α/β-微管蛋白异二聚体已被分离和研究了50多年,但微管蛋白同种型如何促进支持多种细胞结构的微管组织和功能仍然是一个基本问题。为了填补这一知识空白,已采用用纯化的α/β-微管蛋白重组微管进行生化和生物物理表征。这些分析为微管动力学、稳定性以及与其他相关蛋白相互作用的调控提供了机制性见解。在这里,我们综述了生成纯化α/β-微管蛋白异二聚体的不断发展的策略,并强调了微管蛋白生物化学的进展,这些进展揭示了微管蛋白同种型在决定微管结构和特性中的作用。