6RH6

Solution structure and 1H, 13C and 15N chemical shift assignments for the complex of NECAP1 PHear domain with phosphorylated AP2 mu2 148-163

6RH6 の概要

• エントリーDOI: 10.2210/pdb6rh6/pdb
• NMR情報: BMRB: 34395
• 分子名称: Adaptin ear-binding coat-associated protein 1, AP-2 complex subunit mu (2 entities in total)
• 機能のキーワード: clathrin mediated endocytosis, regulation by phosphorylation, ap2 endocytic adaptor, necap, snx9, endocytosis
• 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: 17361.26

構造登録者

Owen, D.J.,Neuhaus, D.,Yang, J.-C.,Herrmann, T. (登録日: 2019-04-18, 公開日: 2019-09-04, 最終更新日: 2024-11-13)

主引用文献

Wrobel, A.G.,Kadlecova, Z.,Kamenicky, J.,Yang, J.C.,Herrmann, T.,Kelly, B.T.,McCoy, A.J.,Evans, P.R.,Martin, S.,Muller, S.,Sroubek, F.,Neuhaus, D.,Honing, S.,Owen, D.J.
Temporal Ordering in Endocytic Clathrin-Coated Vesicle Formation via AP2 Phosphorylation.
Dev.Cell, 50:494-508.e11, 2019

PubMed Abstract: Clathrin-mediated endocytosis (CME) is key to maintaining the transmembrane protein composition of cells' limiting membranes. During mammalian CME, a reversible phosphorylation event occurs on Thr156 of the μ2 subunit of the main endocytic clathrin adaptor, AP2. We show that this phosphorylation event starts during clathrin-coated pit (CCP) initiation and increases throughout CCP lifetime. μ2Thr156 phosphorylation favors a new, cargo-bound conformation of AP2 and simultaneously creates a binding platform for the endocytic NECAP proteins but without significantly altering AP2's cargo affinity in vitro. We describe the structural bases of both. NECAP arrival at CCPs parallels that of clathrin and increases with μ2Thr156 phosphorylation. In turn, NECAP recruits drivers of late stages of CCP formation, including SNX9, via a site distinct from where NECAP binds AP2. Disruption of the different modules of this phosphorylation-based temporal regulatory system results in CCP maturation being delayed and/or stalled, hence impairing global rates of CME.

PubMed: 31430451
DOI: 10.1016/j.devcel.2019.07.017

実験手法

SOLUTION NMR