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Article Dans Une Revue Proceedings of the National Academy of Sciences of the United States of America Année : 2021

Molecular insights into mechanisms of GPCR hijacking by Staphylococcus aureus

Résumé

Atypical chemokine receptor 1 (ACKR1) is a G protein–coupled receptor (GPCR) targeted by Staphylococcus aureus bicomponent pore-forming leukotoxins to promote bacterial growth and immune evasion. Here, we have developed an integrative molecular pharmacology and structural biology approach in order to characterize the effect of leukotoxins HlgA and HlgB on ACKR1 structure and function. Interestingly, using cell-based assays and native mass spectrometry, we found that both components HlgA and HlgB compete with endogenous chemokines through a direct binding with the extracellular domain of ACKR1. Unexpectedly, hydrogen/deuterium exchange mass spectrometry analysis revealed that toxin binding allosterically modulates the intracellular G protein–binding domain of the receptor, resulting in dissociation and/or changes in the architecture of ACKR1−Gαi1 protein complexes observed in living cells. Altogether, our study brings important molecular insights into the initial steps of leukotoxins targeting a host GPCR.
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Dates et versions

hal-03426718 , version 1 (12-11-2021)

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Claire Grison, Paul Lambey, Sylvain Jeannot, Elise del Nero, Simon Fontanel, et al.. Molecular insights into mechanisms of GPCR hijacking by Staphylococcus aureus. Proceedings of the National Academy of Sciences of the United States of America, 2021, 118 (42), pp.e2108856118. ⟨10.1073/pnas.2108856118⟩. ⟨hal-03426718⟩
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