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YidC Insertase of Escherichia coli: Water Accessibility and Membrane Shaping.
- Source :
-
Structure (London, England : 1993) [Structure] 2017 Sep 05; Vol. 25 (9), pp. 1403-1414.e3. Date of Electronic Publication: 2017 Aug 24. - Publication Year :
- 2017
-
Abstract
- The YidC/Oxa1/Alb3 family of membrane proteins function to insert proteins into membranes in bacteria, mitochondria, and chloroplasts. Recent X-ray structures of YidC from Bacillus halodurans and Escherichia coli revealed a hydrophilic groove that is accessible from the lipid bilayer and the cytoplasm. Here, we explore the water accessibility within the conserved core region of the E. coli YidC using in vivo cysteine alkylation scanning and molecular dynamics (MD) simulations of YidC in POPE/POPG membranes. As expected from the structure, YidC possesses an aqueous membrane cavity localized to the membrane inner leaflet. Both the scanning data and the MD simulations show that the lipid-exposed transmembrane helices 3, 4, and 5 are short, leading to membrane thinning around YidC. Close examination of the MD data reveals previously unrecognized structural features that are likely important for protein stability and function.<br /> (Copyright © 2017 Elsevier Ltd. All rights reserved.)
- Subjects :
- Alkylation
Cell Membrane metabolism
Crystallography, X-Ray
Cysteine chemistry
Escherichia coli chemistry
Models, Molecular
Molecular Dynamics Simulation
Protein Stability
Protein Structure, Secondary
Escherichia coli enzymology
Escherichia coli Proteins chemistry
Escherichia coli Proteins metabolism
Membrane Transport Proteins chemistry
Membrane Transport Proteins metabolism
Water metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1878-4186
- Volume :
- 25
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Structure (London, England : 1993)
- Publication Type :
- Academic Journal
- Accession number :
- 28844594
- Full Text :
- https://doi.org/10.1016/j.str.2017.07.008