Format

Send to

Choose Destination
Sci Rep. 2018 Sep 10;8(1):13540. doi: 10.1038/s41598-018-31422-5.

Analyzing protein topology based on Laguerre tessellation of a pore-traversing water network.

Author information

1
LPTM, CNRS UMR 8089, Université de Cergy-Pontoise, 95302, Cergy-Pontoise, France. esque@insa-toulouse.fr.
2
LISBP, Université de Toulouse, CNRS, INSA, INRA, 135 Avenue de Rangueil, 31400, Toulouse, France. esque@insa-toulouse.fr.
3
Department of Biochemistry, University of Oxford, South Parks Road, Oxford, OX1 3QU, United Kingdom.
4
Laboratoire de Biochimie Théorique, CNRS, UPR9080, Univ Paris Diderot, Sorbonne Paris Cité, 13 rue Pierre et Marie Curie, 75005, Paris, France.
5
LPTM, CNRS UMR 8089, Université de Cergy-Pontoise, 95302, Cergy-Pontoise, France. oguey@ptm.u-cergy.fr.

Abstract

Given the tight relation between protein structure and function, we present a set of methods to analyze protein topology, implemented in the VLDP program, relying on Laguerre space partitions built from series of molecular dynamics snapshots. The Laguerre partition specifies inter-atomic contacts, formalized in graphs. The deduced properties are the existence and count of water aggregates, possible passage ways and constrictions, the structure, connectivity, stability and depth of the water network. As a test-case, the membrane protein FepA is investigated in its full environment, yielding a more precise description of the protein surface. Inside FepA, the solvent splits into isolated clusters and an intricate network connecting both sides of the lipid bilayer. The network is dynamic, connections set on and off, occasionally substantially relocating traversing paths. Subtle differences are detected between two forms of FepA, ligand-free and complexed with its natural iron carrier, the enterobactin. The complexed form has more constricted and more centered openings in the upper part whereas, in the lower part, constriction is released: two main channels between the plug and barrel lead directly to the periplasm. Reliability, precision and the variety of topological features are the main interest of the method.

PMID:
30202114
PMCID:
PMC6131185
DOI:
10.1038/s41598-018-31422-5
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Nature Publishing Group Icon for PubMed Central
Loading ...
Support Center