5XEQ

Crystal Structure of human MDGA1 and human neuroligin-2 complex

5XEQ の概要

• エントリーDOI: 10.2210/pdb5xeq/pdb
• 分子名称: Neuroligin-2, MAM domain-containing glycosylphosphatidylinositol anchor protein 1, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total)
• 機能のキーワード: immunogloubulin-like domain, cell adhesion
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 100227.79

構造登録者

Kim, H.M.,Kim, J.A.,Kim, D. (登録日: 2017-04-05, 公開日: 2017-07-12, 最終更新日: 2024-10-30)

主引用文献

Kim, J.A.,Kim, D.,Won, S.Y.,Han, K.A.,Park, D.,Cho, E.,Yun, N.,An, H.J.,Um, J.W.,Kim, E.,Lee, J.O.,Ko, J.,Kim, H.M.
Structural Insights into Modulation of Neurexin-Neuroligin Trans-synaptic Adhesion by MDGA1/Neuroligin-2 Complex
Neuron, 94:1121-1131.e6, 2017

PubMed Abstract: Membrane-associated mucin domain-containing glycosylphosphatidylinositol anchor proteins (MDGAs) bind directly to neuroligin-1 (NL1) and neuroligin-2 (NL2), thereby respectively regulating excitatory and inhibitory synapse development. However, the mechanisms by which MDGAs modulate NL activity to specify development of the two synapse types remain unclear. Here, we determined the crystal structures of human NL2/MDGA1 Ig1-3 complex, revealing their stable 2:2 arrangement with three interaction interfaces. Cell-based assays using structure-guided, site-directed MDGA1 mutants showed that all three contact patches were required for the MDGA's negative regulation of NL2-mediated synaptogenic activity. Furthermore, MDGA1 competed with neurexins for NL2 via its Ig1 domain. The binding affinities of both MDGA1 and MDGA2 for NL1 and NL2 were similar, consistent with the structural prediction of similar binding interfaces. However, MDGA1 selectively associated with NL2, but not NL1, in vivo. These findings collectively provide structural insights into the mechanism by which MDGAs negatively modulate synapse development governed by NLs/neurexins.

PubMed: 28641111
DOI: 10.1016/j.neuron.2017.05.034

実験手法

X-RAY DIFFRACTION (3.136 Å)