9Q1V
Crystal Structure of de novo design FimH minibinder F7 complex
9Q1V の概要
エントリーDOI | 10.2210/pdb9q1v/pdb |
分子名称 | FimH minibinder F7, Type 1 fimbrin D-mannose specific adhesin (3 entities in total) |
機能のキーワード | de novo design, multidrug-resistant, bacterial infections, bacterial adhesins, miniprotein inhibitors, de novo protein |
由来する生物種 | synthetic construct 詳細 |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 49010.73 |
構造登録者 | |
主引用文献 | Chazin-Gray, A.M.,Thompson, T.R.,Lopatto, E.D.B.,Magala, P.,Erickson, P.W.,Hunt, A.C.,Manchenko, A.,Aprikian, P.,Tchesnokova, V.,Basova, I.,Sanick, D.A.,Tamadonfar, K.O.,Timm, M.R.,Pinkner, J.S.,Dodson, K.W.,Kang, A.,Joyce, E.,Bera, A.K.,Schmitz, A.J.,Ellebedy, A.H.,Hvorecny, K.L.,Cartwright, M.J.,Vernet, A.,Bardales, S.,White, D.,Klevit, R.E.,Sokurenko, E.V.,Hultgren, S.J.,Baker, D. De Novo Design of Miniprotein Inhibitors of Bacterial Adhesins. Biorxiv, 2025 Cited by PubMed Abstract: The rise of multidrug-resistant bacterial infections necessitates the discovery of novel antimicrobial strategies. Here, we show that protein design provides a generalizable means of generating new antimicrobials by neutralizing the function of bacterial adhesins, which are virulence factors critical in host-pathogen interactions. We designed high-affinity miniprotein binders to FimH and Abp1D/Abp2D chaperone usher pili adhesins from uropathogenic and , respectively, which are implicated in mediating both uncomplicated and catheter-associated urinary tract infections (UTI) responsible for significant morbidity and mortality worldwide. The designed antagonists have high specificity and stability, disrupt bacterial recognition of host receptors, block biofilm formation, and are effective in treating and preventing uncomplicated and catheter-associated UTIs . Targeting virulence factors outside the cell membrane with protein design provides a rapid route to next-generation therapeutics that can disrupt pathogenesis and thus are capable of treating and preventing disease in an antibiotic-sparing manner. PubMed: 40894640DOI: 10.1101/2025.08.18.670751 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.75 Å) |
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