Duan Daisy, Koleske Anthony J
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06510, USA.
Department of Neuroscience, Yale University, New Haven, CT 06510, USA.
J Cell Sci. 2024 Dec 15;137(24). doi: 10.1242/jcs.263470. Epub 2024 Dec 13.
Protein liquid-liquid phase separation (LLPS) is driven by intrinsically disordered regions and multivalent binding domains, both of which are common features of diverse microtubule (MT) regulators. Many in vitro studies have dissected the mechanisms by which MT-binding proteins (MBPs) regulate MT nucleation, stabilization and dynamics, and investigated whether LLPS plays a role in these processes. However, more recent in vivo studies have focused on how MBP LLPS affects biological functions throughout neuronal development. Dysregulation of MBP LLPS can lead to formation of aggregates - an underlying feature in many neurodegenerative diseases - such as the tau neurofibrillary tangles present in Alzheimer's disease. In this Review, we highlight progress towards understanding the regulation of MT dynamics through the lens of phase separation of MBPs and associated cytoskeletal regulators, from both in vitro and in vivo studies. We also discuss how LLPS of MBPs regulates neuronal development and maintains homeostasis in mature neurons.
蛋白质液-液相分离(LLPS)由内在无序区域和多价结合结构域驱动,这两者都是多种微管(MT)调节因子的共同特征。许多体外研究剖析了微管结合蛋白(MBP)调节微管成核、稳定和动力学的机制,并研究了液-液相分离是否在这些过程中发挥作用。然而,最近的体内研究集中在MBP的液-液相分离如何在整个神经元发育过程中影响生物学功能。MBP液-液相分离的失调会导致聚集体的形成——这是许多神经退行性疾病的一个潜在特征——比如阿尔茨海默病中出现的tau神经原纤维缠结。在这篇综述中,我们重点介绍了从体外和体内研究两方面,在通过MBP和相关细胞骨架调节因子的相分离来理解微管动力学调控方面取得的进展。我们还讨论了MBP的液-液相分离如何调节神经元发育并维持成熟神经元的体内平衡。