Interaction of e. coli outer‐membrane protein A with sugars on the receptors of the brain microvascular endothelial cells
- 9 December 2002
- journal article
- research article
- Published by Wiley in Proteins-Structure Function and Bioinformatics
- Vol. 50 (2) , 213-221
- https://doi.org/10.1002/prot.10257
Abstract
Esherichia coli, the most common gram‐negative bacteria, can penetrate the brain microvascular endothelial cells (BMECs) during the neonatal period to cause meningitis with significant morbidity and mortality. Experimental studies have shown that outer‐membrane protein A (OmpA) of E. coli plays a key role in the initial steps of the invasion process by binding to specific sugar moieties present on the glycoproteins of BMEC. These experiments also show that polymers of chitobiose (GlcNAcβ1‐4GlcNAc) block the invasion, while epitopes substituted with the L‐fucosyl group do not. We used HierDock computational technique that consists of a hierarchy of coarse grain docking method with molecular dynamics (MD) to predict the binding sites and energies of interactions of GlcNAcβ1‐4GlcNAc and other sugars with OmpA. The results suggest two important binding sites for the interaction of carbohydrate epitopes of BMEC glycoproteins to OmpA. We identify one site as the binding pocket for chitobiose (GlcNAcβ1‐4GlcNAc) in OmpA, while the second region (including loops 1 and 2) may be important for recognition of specific sugars. We find that the site involving loops 1 and 2 has relative binding energies that correlate well with experimental observations. This theoretical study elucidates the interaction sites of chitobiose with OmpA and the binding site predictions made in this article are testable either by mutation studies or invasion assays. These results can be further extended in suggesting possible peptide antagonists and drug design for therapeutic strategies. Proteins 2003;50:213–221.Keywords
This publication has 31 references indexed in Scilit:
- Stabilization of Coiled-Coil Peptide Domains by Introduction of TrifluoroleucineBiochemistry, 2001
- High-resolution structure of the OmpA membrane domainJournal of Molecular Biology, 2000
- Generalized Born Model Based on a Surface Integral FormulationThe Journal of Physical Chemistry B, 1998
- Structure of the outer membrane protein A transmembrane domainNature Structural & Molecular Biology, 1998
- Substrate Distortion to a Boat Conformation at Subsite −1 Is Critical in the Mechanism of Family 18 ChitinasesJournal of the American Chemical Society, 1998
- All-Atom Empirical Potential for Molecular Modeling and Dynamics Studies of ProteinsThe Journal of Physical Chemistry B, 1998
- Accurate First Principles Calculation of Molecular Charge Distributions and Solvation Energies from Ab Initio Quantum Mechanics and Continuum Dielectric TheoryJournal of the American Chemical Society, 1994
- Gram-negative enteric bacillary meningitis: A twenty-one-year experienceThe Journal of Pediatrics, 1993
- Charge equilibration for molecular dynamics simulationsThe Journal of Physical Chemistry, 1991
- A geometric approach to macromolecule-ligand interactionsJournal of Molecular Biology, 1982