| Literature DB >> 30661983 |
Xiandeng Wu1, Qixu Cai1, Zeyu Shen1, Xudong Chen1, Menglong Zeng1, Shengwang Du2, Mingjie Zhang3.
Abstract
Both the timing and kinetics of neurotransmitter release depend on the positioning of clustered Ca2+ channels in active zones to docked synaptic vesicles on presynaptic plasma membranes. However, how active zones form is not known. Here, we show that RIM and RIM-BP, via specific multivalent bindings, form dynamic and condensed assemblies through liquid-liquid phase separation. Voltage-gated Ca2+ channels (VGCCs), via C-terminal-tail-mediated direct binding to both RIM and RIM-BP, can be enriched to the RIM and RIM-BP condensates. We further show that RIM and RIM-BP, together with VGCCs, form dense clusters on the supported lipid membrane bilayers via phase separation. Therefore, RIMs and RIM-BPs are plausible organizers of active zones, and the formation of RIM and RIM-BP condensates may cluster VGCCs into nano- or microdomains and position the clustered Ca2+ channels with Ca2+ sensors on docked vesicles for efficient and precise synaptic transmissions.Entities:
Keywords: RIM; RIM-BP; biological condensates; liquid-liquid phase transition; membraneless compartments; neurotransmitter release; presynaptic active zone; scaffold proteins
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Year: 2019 PMID: 30661983 DOI: 10.1016/j.molcel.2018.12.007
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970