Department of Chemistry, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Korea.
Graduate School of Medical Science & Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Korea.
Mol Cells. 2018 Jul 31;41(7):622-630. doi: 10.14348/molcells.2018.0202. Epub 2018 Jul 11.
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 -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.
白细胞共同抗原相关蛋白酪氨酸磷酸酶 (LAR-RPTPs) 是肝素硫酸盐 (HS) 和软骨素硫酸盐 (CS) 蛋白聚糖的细胞受体,可调节轴突生长和神经元再生。LAR-RPTPs 还因其作为主要的突触前枢纽而受到特别关注,通过选择性结合许多突触后粘附伙伴来组织突触。最近对 LAR-RPTP 介导的 -突触粘附复合物的结构研究为其特异性相互作用的分子基础、选择性结合的关键代码以及 LAR-RPTP 用于突触发生必需的高级聚类提供了重要的见解。在这篇综述中,我们总结了 LAR-RPTP 与各种突触后粘附伙伴形成复合物的结构,并讨论了 LAR-RPTP 介导的突触发生的分子机制。