Visualizing conformation transitions of the Lipid II flippase MurJ.
The biosynthesis of many polysaccharides, including bacterial peptidoglycan and eukaryotic N-linked glycans, requires transport of lipid-linked oligosaccharide (LLO) precursors across the membrane by specialized flippases. MurJ is the flippase for the lipid-linked peptidoglycan precursor Lipid II, a key player in bacterial cell wall synthesis, and a target of recently discovered antibacterials. However, the flipping mechanism of LLOs including Lipid II remains poorly understood due to a dearth of structural information. Here we report crystal structures of MurJ captured in inward-closed, inward-open, inward-occluded and outward-facing conformations. Together with mutagenesis studies, we elucidate the conformational transitions in MurJ that mediate lipid flipping, identify the key ion for function, and provide a framework for the development of inhibitors.
Duke Scholars
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- Protein Domains
- Protein Conformation
- Phospholipid Transfer Proteins
- Mutagenesis, Site-Directed
- Models, Molecular
- Escherichia coli Proteins
- Escherichia coli
- Crystallography, X-Ray
Citation
Published In
DOI
EISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Protein Domains
- Protein Conformation
- Phospholipid Transfer Proteins
- Mutagenesis, Site-Directed
- Models, Molecular
- Escherichia coli Proteins
- Escherichia coli
- Crystallography, X-Ray