Proteomics

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Structural basis of gate dynamics at the outer membrane lipopolysaccharide holo-translocon

ABSTRACT: Gram-negative bacteria resist many harmful chemicals, protected by an asymmetric outer membrane (OM) containing lipopolysaccharide (LPS) in its external leaflet. Leaflet-selective assembly of LPS is an essential, yet mechanistically elusive process. This reaction is mediated by the OM LPS core translocon, composed of the transmembrane protein LptD and its cognate lipoprotein LptE. Here, we characterize two additional translocon subunits, the lipoproteins LptM and YedD, uncovering their impact on LptD conformational dynamics. This dataset includes native MS allowing the identification of YedD, after gas-phase dissociation from the LptDE/LptDEM complexes (complex-down MS). We also include here bottom-up proteomics data after trypsin digestion from SDS-PAGE gel bands, confirming the nature of YedD in the purified complex.

INSTRUMENT(S):

ORGANISM(S): Escherichia Coli

SUBMITTER: Julien Marcoux  

LAB HEAD: Julien Marcoux

PROVIDER: PXD068376 | Pride | 2025-12-01

REPOSITORIES: Pride

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Action DRS
F143324.dat Other
F143325.dat Other
F143326.dat Other
F143327.dat Other
QEMMR241120_R_22.raw Raw
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Publications

Lipopolysaccharide (LPS) assembly at the surfaces-exposed leaflet of the bacterial outer membrane (OM) is mediated by the OM LPS translocon. An essential transmembrane β-barrel protein, LptD, and a cognate lipoprotein, LptE, translocate LPS selectively into the OM external leaflet via a poorly understood mechanism. Here, we characterize two additional translocon subunits, the lipoproteins LptM and LptY (formerly YedD). We use single-particle cryo-EM analysis, functional assays and molecular dyna  ...[more]

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