State Key Laboratory of Natural and Biomimetic Drugs, 38 Xueyuan Road, Haidian District, Beijing 100191, China; Department of Molecular and Cellular Pharmacology, School of Pharmaceutical Sciences, Peking University Health Science Center, 38 Xueyuan Road, Haidian District, Beijing 100191, China.
Curr Opin Struct Biol. 2019 Feb;54:59-67. doi: 10.1016/j.sbi.2019.01.002. Epub 2019 Feb 8.
Synaptic adhesion-like molecules (SALMs), also known as leucine-rich repeat and fibronectin III domain-containing proteins (LRFNs), are a family of synaptic adhesion molecules that consist of five members. SALMs exhibit functions in regulating neurite outgrowth and branching, synapse formation, and synapse maturation. Recent clinical studies have shown an association of SALMs with diverse neurological disorders. In this review article, we summarize structural mechanisms of the interaction of SALMs with leukocyte common antigen (LAR) family receptor tyrosine phosphatases (LAR-RPTPs) for synaptic activity, based on recent advances in the structural biology of SALMs.
突触黏附样分子(SALMs),也称为富含亮氨酸重复和纤维连接蛋白 III 结构域蛋白(LRFNs),是一个由五个成员组成的突触黏附分子家族。SALMs 在调节轴突生长和分支、突触形成和突触成熟方面发挥作用。最近的临床研究表明,SALMs 与多种神经疾病有关。在这篇综述文章中,我们根据 SALMs 的结构生物学的最新进展,总结了 SALMs 与白细胞共同抗原(LAR)家族受体酪氨酸磷酸酶(LAR-RPTPs)相互作用的结构机制,以调节突触活性。