The Helicobacter pylori adhesin protein HopQ exploits the dimer interface of human CEACAMs to facilitate translocation of the oncoprotein CagA
Autor: | Dorothy Beckett, Daniel Deredge, Robert Beadenkopf, Rainer Haas, Blaine J. Dow, Qing Zhao, Daniel A. Bonsor, Patrick L. Wintrode, Barbara Schmidinger, Evelyn Weiss, Jingheng Wang, Eric J. Sundberg, Wolfgang Fischer |
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Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
education.field_of_study 030102 biochemistry & molecular biology General Immunology and Microbiology biology General Neuroscience Mutagenesis Population Chromosomal translocation Helicobacter pylori biology.organism_classification General Biochemistry Genetics and Molecular Biology Cell biology Bacterial adhesin 03 medical and health sciences 030104 developmental biology CagA Secretion education Cell adhesion Molecular Biology |
Zdroj: | The EMBO Journal. 37 |
ISSN: | 1460-2075 0261-4189 |
DOI: | 10.15252/embj.201798664 |
Popis: | Helicobacter pylori infects half of the world's population, and strains that encode the cag type IV secretion system for injection of the oncoprotein CagA into host gastric epithelial cells are associated with elevated levels of cancer. CagA translocation into host cells is dependent on interactions between the H. pylori adhesin protein HopQ and human CEACAMs. Here, we present high-resolution structures of several HopQ-CEACAM complexes and CEACAMs in their monomeric and dimeric forms establishing that HopQ uses a coupled folding and binding mechanism to engage the canonical CEACAM dimerization interface for CEACAM recognition. By combining mutagenesis with biophysical and functional analyses, we show that the modes of CEACAM recognition by HopQ and CEACAMs themselves are starkly different. Our data describe precise molecular mechanisms by which microbes exploit host CEACAMs for infection and enable future development of novel oncoprotein translocation inhibitors and H. pylori-specific antimicrobial agents. |
Databáze: | OpenAIRE |
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