Structural Basis for LAR-RPTP-Mediated Synaptogenesis

被引:10
作者
Won, Seoung Youn [1 ]
Kim, Ho Min [2 ,3 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem, Daejeon 34141, South Korea
[2] Korea Adv Inst Sci & Technol, Grad Sch Med Sci & Engn, Daejeon 34141, South Korea
[3] Inst for Basic Sci Korea, Ctr Synapt Brain Dysfunct, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
heparan sulfate; higher-order clustering; LAR-RPTPs; LAR-RPTP-mediated trans-synaptic adhesion complex; synaptic adhesion molecules; PROTEIN-TYROSINE-PHOSPHATASES; SYNAPTIC ADHESION MOLECULES; RAT HIPPOCAMPAL-NEURONS; PTP-SIGMA; CRYSTAL-STRUCTURE; TRANSSYNAPTIC INTERACTION; INTERLEUKIN-1; RECEPTOR; MENTAL-RETARDATION; COMPLEX; FAMILY;
D O I
10.14348/molcells.2018.0202
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
Leukocyte common antigen-related protein tyrosine phosphatases (LAR-RPTPs) are cellular receptors of heparan sulfate (HS) and chondroitin sulfate (CS) proteoglycans that regulate neurite outgrowth and neuronal regeneration. LAR-RPTPs have also received particular attention as the major presynaptic hubs for synapse organization through selective binding to numerous postsynaptic adhesion partners. Recent structural studies on LAR-RPTP-mediated trans-synaptic adhesion complexes have provided significant insight into the molecular basis of their specific interactions, the key codes for their selective binding, as well as the higher-order clustering of LAR-RPTPs necessary for synaptogenic activity. In this review, we summarize the structures of LAR-RPTPs in complex with various postsynaptic adhesion partners and discuss the molecular mechanisms underlying LAR-RPTP-mediated synaptogenesis.
引用
收藏
页码:622 / 630
页数:9
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