Intrinsically disordered proteins in synaptic vesicle trafficking and release

被引:51
作者
Snead, David [1 ]
Eliezer, David [1 ]
机构
[1] Weill Cornell Med, Dept Biochem, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
intrinsically disordered protein; neurotransmitter release; lipid vesicle; protein folding; membrane trafficking; -synuclein; complexin; membraneless organelles; phase transitions; synaptic vesicles; BOUND ALPHA-SYNUCLEIN; N-TERMINAL ACETYLATION; SPONTANEOUS NEUROTRANSMITTER RELEASE; LIPID-BINDING DOMAIN; PARKINSONS-DISEASE; SNARE-COMPLEX; MEMBRANE CURVATURE; WILD-TYPE; MOLECULAR RECOGNITION; PHOSPHOLIPID-BINDING;
D O I
10.1074/jbc.REV118.006493
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The past few years have resulted in an increased awareness and recognition of the prevalence and roles of intrinsically disordered proteins and protein regions (IDPs and IDRs, respectively) in synaptic vesicle trafficking and exocytosis and in overall synaptic organization. IDPs and IDRs constitute a class of proteins and protein regions that lack stable tertiary structure, but nevertheless retain biological function. Their significance in processes such as cell signaling is now well accepted, but their pervasiveness and importance in other areas of biology are not as widely appreciated. Here, we review the prevalence and functional roles of IDPs and IDRs associated with the release and recycling of synaptic vesicles at nerve terminals, as well as with the architecture of these terminals. We hope to promote awareness, especially among neuroscientists, of the importance of this class of proteins in these critical pathways and structures. The examples discussed illustrate some of the ways in which the structural flexibility conferred by intrinsic protein disorder can be functionally advantageous in the context of cellular trafficking and synaptic function.
引用
收藏
页码:3325 / 3342
页数:18
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