7USM

Integrin alphaM/beta2 ectodomain

7USM の概要

• エントリーDOI: 10.2210/pdb7usm/pdb
• EMDBエントリー: 26739
• 分子名称: Integrin alpha-M, Integrin beta, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (5 entities in total)
• 機能のキーワード: integrin, complement, receptor, 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: 211815.81

構造登録者

Goldsmith, J.A.,McLellan, J.S. (登録日: 2022-04-25, 公開日: 2022-08-17, 最終更新日: 2024-10-30)

主引用文献

Goldsmith, J.A.,DiVenere, A.M.,Maynard, J.A.,McLellan, J.S.
Structural basis for non-canonical integrin engagement by Bordetella adenylate cyclase toxin.
Cell Rep, 40:111196-111196, 2022

PubMed Abstract: Integrins are ubiquitous cell-surface heterodimers that are exploited by pathogens and toxins, including leukotoxins that target β integrins on phagocytes. The Bordetella adenylate cyclase toxin (ACT) uses the αβ integrin as a receptor, but the structural basis for integrin binding and neutralization by antibodies is poorly understood. Here, we use cryoelectron microscopy to determine a 2.7 Å resolution structure of an ACT fragment bound to αβ. This structure reveals that ACT interacts with the headpiece and calf-2 of the α subunit in a non-canonical manner specific to bent, inactive αβ. Neutralizing antibody epitopes map to ACT residues involved in α binding, providing the basis for antibody-mediated attachment inhibition. Furthermore, binding to αβ positions the essential ACT acylation sites, which are conserved among toxins exported by type I secretion systems, at the cell membrane. These findings reveal a structural mechanism for integrin-mediated attachment and explain antibody-mediated neutralization of ACT intoxication.

PubMed: 35977491
DOI: 10.1016/j.celrep.2022.111196

実験手法

ELECTRON MICROSCOPY (2.7 Å)