Su-yin, Kan and Miriam, Walden and John M, Edwards (2015) An internal thioester in a pathogen surface protein mediates covalent host binding. eLife, 4. pp. 1-24. ISSN 2050084X
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Abstract
To cause disease and persist in a host, pathogenic and commensal microbes must adhere to tissues. Colonization and infection depend on specific molecular interactions at the host-microbe interface that involve microbial surface proteins, or adhesins. To date, adhesins are only known to bind to host receptors non-covalently. Here we show that the streptococcal surface protein SfbI mediates covalent interaction with the host protein fibrinogen using an unusual internal thioester bond as a ‘chemical harpoon’. This cross-linking reaction allows bacterial attachment to fibrin and SfbI binding to human cells in a model of inflammation. Thioester-containing domains are unexpectedly prevalent in Gram-positive bacteria, including many clinically relevant pathogens. Our findings support bacterial-encoded covalent binding as a new molecular principle in host-microbe interactions. This represents an as yet unexploited target to treat bacterial infection and may also offer novel opportunities for engineering beneficial interactions.
Item Type: | Article |
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Uncontrolled Keywords: | Clostridium perfringens; Streptococcus pneumoniae; Streptococcus pyogenes; bacterial surface proteins; biophysics; fibrinogen; host-microbe interactions; infectious disease; microbiology; structural biology |
Subjects: | Q Science > QH Natural history > QH301 Biology |
Divisions: | Faculty of Health Sciences |
Depositing User: | Syahmi Manaf |
Date Deposited: | 13 Sep 2022 05:50 |
Last Modified: | 13 Sep 2022 05:50 |
URI: | http://eprints.unisza.edu.my/id/eprint/6442 |
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