7LT8

Crystal structure of Ras suppressor-1

7LT8 の概要

• エントリーDOI: 10.2210/pdb7lt8/pdb
• 関連するPDBエントリー: 7LT9
• 分子名称: Ras suppressor protein 1 (2 entities in total)
• 機能のキーワード: leucine-rich repeat, cell adhesion
• 由来する生物種: Homo sapiens (Human)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 31861.54

構造登録者

Fukuda, K.,Qin, J. (登録日: 2021-02-19, 公開日: 2021-04-28, 最終更新日: 2024-03-06)

主引用文献

Fukuda, K.,Lu, F.,Qin, J.
Molecular basis for Ras suppressor-1 binding to PINCH-1 in focal adhesion assembly.
J.Biol.Chem., 296:100685-100685, 2021

PubMed Abstract: Ras suppressor-1 (Rsu-1) is a leucine-rich repeat (LRR)-containing protein that is crucial for regulating cell adhesion and is involved in such physiological and pathological processes as focal adhesion assembly and tumor metastasis. Rsu-1 interacts with zinc-finger type multi-LIM domain-containing adaptor protein PINCH-1, known to be involved in the integrin-mediated consensus adhesome, but not with its highly homologous family member PINCH-2. However, the structural basis for and regulatory mechanisms of this specific interaction remain unclear. Here, we determined the crystal structures of Rsu-1 and its complex with the PINCH-1 LIM4-5 domains. Rsu-1 displays an arc-shaped solenoid architecture, with eight LRRs shielded by N- and C-terminal capping modules. We showed that the conserved concave surface of the Rsu-1 LRR domain binds and stabilizes the PINCH-1 LIM5 domain via salt bridge and hydrophobic interactions, while the C-terminal non-LIM region of PINCH-2 sterically disfavors Rsu-1 binding. We also showed that Rsu-1 can be assembled, via PINCH-1-binding, into a heteropentamer complex comprising Rsu-1, PINCH-1, ILK, Parvin, and Kindlin-2, which constitute a major consensus integrin adhesome crucial for focal adhesion assembly. Our mutagenesis and cell biological data emphasize the significance of the Rsu-1/PINCH-1 interaction in focal adhesion assembly and cell spreading, providing crucial molecular insights into Rsu-1-mediated cell adhesion with implications for disease development.

PubMed: 33891945
DOI: 10.1016/j.jbc.2021.100685

実験手法

X-RAY DIFFRACTION (1.76000247097 Å)