Direct observation of the influence of cardiolipin and antibiotics on lipid II binding to MurJ

Translocation of lipid II across cytoplasmic membrane is essential in peptidoglycan biogenesis. While most steps are understood, identifying the lipid II flippase has yielded conflicting results and the lipid II binding properties of two candidate flippases, MurJ and FtsW, remain largely unknown. He...

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Main Authors: Bolla, J, Sauer, J, Wu, D, Mehmood, S, Allison, T, Robinson, C
Format: Journal article
Published: Nature Publishing Group 2018
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author Bolla, J
Sauer, J
Wu, D
Mehmood, S
Allison, T
Robinson, C
author_facet Bolla, J
Sauer, J
Wu, D
Mehmood, S
Allison, T
Robinson, C
author_sort Bolla, J
collection OXFORD
description Translocation of lipid II across cytoplasmic membrane is essential in peptidoglycan biogenesis. While most steps are understood, identifying the lipid II flippase has yielded conflicting results and the lipid II binding properties of two candidate flippases, MurJ and FtsW, remain largely unknown. Here we apply native mass spectrometry to both proteins and characterise lipid II binding. We observed lower levels of lipid II binding to FtsW compared to MurJ, consistent with MurJ having a higher affinity. Site directed mutagenesis of MurJ suggests that mutations at A29 and D269 attenuate, and chemical modification of A29 eliminate, lipid II binding to MurJ. The antibiotic ramoplanin dissociates lipid II from MurJ whereas vancomycin binds to form a stable complex with MurJ:lipid II. Furthermore, we reveal cardiolipins associate with MurJ but not FtsW, and exogenous cardiolipins reduce lipid II binding to MurJ. These observations provide insights into determinants of lipid II binding to MurJ and suggest roles for endogenous lipids in regulating substrate binding
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spelling oxford-uuid:0167dce3-fb7e-47db-a40e-6f0d9d3740fa2022-03-26T08:34:47ZDirect observation of the influence of cardiolipin and antibiotics on lipid II binding to MurJJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:0167dce3-fb7e-47db-a40e-6f0d9d3740faSymplectic Elements at OxfordNature Publishing Group2018Bolla, JSauer, JWu, DMehmood, SAllison, TRobinson, CTranslocation of lipid II across cytoplasmic membrane is essential in peptidoglycan biogenesis. While most steps are understood, identifying the lipid II flippase has yielded conflicting results and the lipid II binding properties of two candidate flippases, MurJ and FtsW, remain largely unknown. Here we apply native mass spectrometry to both proteins and characterise lipid II binding. We observed lower levels of lipid II binding to FtsW compared to MurJ, consistent with MurJ having a higher affinity. Site directed mutagenesis of MurJ suggests that mutations at A29 and D269 attenuate, and chemical modification of A29 eliminate, lipid II binding to MurJ. The antibiotic ramoplanin dissociates lipid II from MurJ whereas vancomycin binds to form a stable complex with MurJ:lipid II. Furthermore, we reveal cardiolipins associate with MurJ but not FtsW, and exogenous cardiolipins reduce lipid II binding to MurJ. These observations provide insights into determinants of lipid II binding to MurJ and suggest roles for endogenous lipids in regulating substrate binding
spellingShingle Bolla, J
Sauer, J
Wu, D
Mehmood, S
Allison, T
Robinson, C
Direct observation of the influence of cardiolipin and antibiotics on lipid II binding to MurJ
title Direct observation of the influence of cardiolipin and antibiotics on lipid II binding to MurJ
title_full Direct observation of the influence of cardiolipin and antibiotics on lipid II binding to MurJ
title_fullStr Direct observation of the influence of cardiolipin and antibiotics on lipid II binding to MurJ
title_full_unstemmed Direct observation of the influence of cardiolipin and antibiotics on lipid II binding to MurJ
title_short Direct observation of the influence of cardiolipin and antibiotics on lipid II binding to MurJ
title_sort direct observation of the influence of cardiolipin and antibiotics on lipid ii binding to murj
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