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9CCS

CryoEM Structure of Escherichia coli FimCH in complex with 2H04 Fab

9CCS の概要
エントリーDOI10.2210/pdb9ccs/pdb
EMDBエントリー45456
分子名称Type 1 fimbiral adhesin FimH, 2H04 Fab light chain, 2H04 Fab heavy chain (3 entities in total)
機能のキーワードadhesin, inhibitor, complex, fab, chaperone, usher, pili, cell adhesion
由来する生物種Escherichia coli UTI89
詳細
タンパク質・核酸の鎖数3
化学式量合計79324.18
構造登録者
Lopatto, E.D.B.,Hultgren, S.J. (登録日: 2024-06-23, 公開日: 2025-07-02)
主引用文献Lopatto, E.D.B.,Santiago-Borges, J.M.,Sanick, D.A.,Malladi, S.K.,Azimzadeh, P.N.,Timm, M.W.,Fox, I.F.,Schmitz, A.J.,Turner, J.S.,Sayed Ahmed, S.M.,Ortinau, L.,Gualberto, N.C.,Pinkner, J.S.,Dodson, K.W.,Ellebedy, A.H.,Kau, A.L.,Hultgren, S.J.
Monoclonal antibodies targeting the FimH adhesin protect against uropathogenic E. coli UTI.
Sci Adv, 11:eadw0698-eadw0698, 2025
Cited by
PubMed Abstract: As antimicrobial resistance increases, urinary tract infections (UTIs) are expected to pose an increased burden in morbidity and expense on the health care system, increasing the need for alternative antibiotic-sparing treatments. Most UTIs are caused by uropathogenic (UPEC), whereas causes a large portion of non-UPEC UTIs. Both bacteria express type 1 pili tipped with the mannose-binding FimH adhesin critical for UTI pathogenesis. We generated and biochemically characterized 33 murine monoclonal antibodies (mAbs) to FimH. Three mAbs protected mice from UTI. Mechanistically, we show that this protection is Fc independent and mediated by the ability of these mAbs to sterically block FimH function by recognizing a high-affinity FimH conformation. Our data reveal that FimH mAbs hold promise as an antibiotic-sparing treatment strategy.
PubMed: 40540557
DOI: 10.1126/sciadv.adw0698
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (3.17 Å)
構造検証レポート
Validation report summary of 9ccs
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-07-02に公開中

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