7ML7

Structural basis for CSPG4 as a receptor for TcdB and a therapeutic target in Clostridioides difficile infection

7ML7 の概要

• エントリーDOI: 10.2210/pdb7ml7/pdb
• EMDBエントリー: 23909
• 分子名称: Toxin B, Chondroitin sulfate proteoglycan 4, ZINC ION (3 entities in total)
• 機能のキーワード: cspg4, tcdb, clostridioides difficile infection, toxin
• 由来する生物種: Clostridioides difficile (Peptoclostridium difficile); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 311116.24

構造登録者

Chen, P.,Jin, R. (登録日: 2021-04-27, 公開日: 2021-06-09, 最終更新日: 2024-10-30)

主引用文献

Chen, P.,Zeng, J.,Liu, Z.,Thaker, H.,Wang, S.,Tian, S.,Zhang, J.,Tao, L.,Gutierrez, C.B.,Xing, L.,Gerhard, R.,Huang, L.,Dong, M.,Jin, R.
Structural basis for CSPG4 as a receptor for TcdB and a therapeutic target in Clostridioides difficile infection.
Nat Commun, 12:3748-3748, 2021

PubMed Abstract: C. difficile is a major cause of antibiotic-associated gastrointestinal infections. Two C. difficile exotoxins (TcdA and TcdB) are major virulence factors associated with these infections, and chondroitin sulfate proteoglycan 4 (CSPG4) is a potential receptor for TcdB, but its pathophysiological relevance and the molecular details that govern recognition remain unknown. Here, we determine the cryo-EM structure of a TcdB-CSPG4 complex, revealing a unique binding site spatially composed of multiple discontinuous regions across TcdB. Mutations that selectively disrupt CSPG4 binding reduce TcdB toxicity in mice, while CSPG4-knockout mice show reduced damage to colonic tissues during C. difficile infections. We further show that bezlotoxumab, the only FDA approved anti-TcdB antibody, blocks CSPG4 binding via an allosteric mechanism, but it displays low neutralizing potency on many TcdB variants from epidemic hypervirulent strains due to sequence variations in its epitopes. In contrast, a CSPG4-mimicking decoy neutralizes major TcdB variants, suggesting a strategy to develop broad-spectrum therapeutics against TcdB.

PubMed: 34145250
DOI: 10.1038/s41467-021-23878-3

実験手法

ELECTRON MICROSCOPY (3.17 Å)