Department of Clinical Neurosciences, Cambridge Institute for Medical Research, University of Cambridge, Cambridge CB2 0XY, UK.
Open Biol. 2022 Feb;12(2):210334. doi: 10.1098/rsob.210334. Epub 2022 Feb 9.
Fundamental discoveries have shaped our molecular understanding of presynaptic processes, such as neurotransmitter release, active zone organization and mechanisms of synaptic vesicle (SV) recycling. However, certain regulatory steps still remain incompletely understood. Protein liquid-liquid phase separation (LLPS) and its role in SV clustering and active zone regulation now introduce a new perception of how the presynapse and its different compartments are organized. This article highlights the newly emerging concept of LLPS at the synapse, providing a systematic overview on LLPS tendencies of over 500 presynaptic proteins, spotlighting individual proteins and discussing recent progress in the field. Newly discovered LLPS systems like ELKS/liprin-alpha and Eps15/FCho are put into context, and further LLPS candidate proteins, including epsin1, dynamin, synaptojanin, complexin and rabphilin-3A, are highlighted.
基础发现已经使我们对突触前过程(如神经递质释放、活性区组织和突触小泡(SV)再循环的机制)有了分子水平的理解。然而,某些调节步骤仍然不完全清楚。蛋白质液-液相分离(LLPS)及其在 SV 聚集和活性区调节中的作用,现在为我们提供了一个新的认识,即突触前和其不同隔室是如何组织的。本文强调了突触处 LLPS 的新出现概念,对 500 多种突触前蛋白的 LLPS 倾向进行了系统概述,突出了个别蛋白,并讨论了该领域的最新进展。新发现的 LLPS 系统,如 ELKS/liprin-alpha 和 Eps15/FCho,被置于相应的背景下,进一步的 LLPS 候选蛋白,包括 epsin1、dynamin、synaptojanin、complexin 和 rabphilin-3A,也被强调。