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‘Double water exclusion’: a hypothesis refining the O-ring theory for the hot spots at protein interfaces

Motivation: The O-ring theory reveals that the binding hot spot at a protein interface is surrounded by a ring of residues that are energetically less important than the residues in the hot spot. As this ring of residues is served to occlude water molecules from the hot spot, the O-ring theory is al...

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Autores principales: Li, Jinyan, Liu, Qian
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654803/
https://www.ncbi.nlm.nih.gov/pubmed/19179356
http://dx.doi.org/10.1093/bioinformatics/btp058
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author Li, Jinyan
Liu, Qian
author_facet Li, Jinyan
Liu, Qian
author_sort Li, Jinyan
collection PubMed
description Motivation: The O-ring theory reveals that the binding hot spot at a protein interface is surrounded by a ring of residues that are energetically less important than the residues in the hot spot. As this ring of residues is served to occlude water molecules from the hot spot, the O-ring theory is also called ‘water exclusion’ hypothesis. We propose a ‘double water exclusion’ hypothesis to refine the O-ring theory by assuming the hot spot itself is water-free. To computationally model a water-free hot spot, we use a biclique pattern that is defined as two maximal groups of residues from two chains in a protein complex holding the property that every residue contacts with all residues in the other group. Methods and Results: Given a chain pair A and B of a protein complex from the Protein Data Bank (PDB), we calculate the interatomic distance of all possible pairs of atoms between A and B. We then represent A and B as a bipartite graph based on these distance information. Maximal biclique subgraphs are subsequently identified from all of the bipartite graphs to locate biclique patterns at the interfaces. We address two properties of biclique patterns: a non-redundant occurrence in PDB, and a correspondence with hot spots when the solvent-accessible surface area (SASA) of a biclique pattern in the complex form is small. A total of 1293 biclique patterns are discovered which have a non-redundant occurrence of at least five, and which each have a minimum two and four residues at the two sides. Through extensive queries to the HotSprint and ASEdb databases, we verified that biclique patterns are rich of true hot residues. Our algorithm and results provide a new way to identify hot spots by examining proteins' structural data. Availability: The biclique mining algorithm is available at http://www.ntu.edu.sg/home/jyli/dwe.html. Contact: jyli@ntu.edu.sg Supplementary information: Supplementary data are available at Bioinformatics online.
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spelling pubmed-26548032009-04-02 ‘Double water exclusion’: a hypothesis refining the O-ring theory for the hot spots at protein interfaces Li, Jinyan Liu, Qian Bioinformatics Original Papers Motivation: The O-ring theory reveals that the binding hot spot at a protein interface is surrounded by a ring of residues that are energetically less important than the residues in the hot spot. As this ring of residues is served to occlude water molecules from the hot spot, the O-ring theory is also called ‘water exclusion’ hypothesis. We propose a ‘double water exclusion’ hypothesis to refine the O-ring theory by assuming the hot spot itself is water-free. To computationally model a water-free hot spot, we use a biclique pattern that is defined as two maximal groups of residues from two chains in a protein complex holding the property that every residue contacts with all residues in the other group. Methods and Results: Given a chain pair A and B of a protein complex from the Protein Data Bank (PDB), we calculate the interatomic distance of all possible pairs of atoms between A and B. We then represent A and B as a bipartite graph based on these distance information. Maximal biclique subgraphs are subsequently identified from all of the bipartite graphs to locate biclique patterns at the interfaces. We address two properties of biclique patterns: a non-redundant occurrence in PDB, and a correspondence with hot spots when the solvent-accessible surface area (SASA) of a biclique pattern in the complex form is small. A total of 1293 biclique patterns are discovered which have a non-redundant occurrence of at least five, and which each have a minimum two and four residues at the two sides. Through extensive queries to the HotSprint and ASEdb databases, we verified that biclique patterns are rich of true hot residues. Our algorithm and results provide a new way to identify hot spots by examining proteins' structural data. Availability: The biclique mining algorithm is available at http://www.ntu.edu.sg/home/jyli/dwe.html. Contact: jyli@ntu.edu.sg Supplementary information: Supplementary data are available at Bioinformatics online. Oxford University Press 2009-03-15 2009-01-29 /pmc/articles/PMC2654803/ /pubmed/19179356 http://dx.doi.org/10.1093/bioinformatics/btp058 Text en © 2009 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Papers
Li, Jinyan
Liu, Qian
‘Double water exclusion’: a hypothesis refining the O-ring theory for the hot spots at protein interfaces
title ‘Double water exclusion’: a hypothesis refining the O-ring theory for the hot spots at protein interfaces
title_full ‘Double water exclusion’: a hypothesis refining the O-ring theory for the hot spots at protein interfaces
title_fullStr ‘Double water exclusion’: a hypothesis refining the O-ring theory for the hot spots at protein interfaces
title_full_unstemmed ‘Double water exclusion’: a hypothesis refining the O-ring theory for the hot spots at protein interfaces
title_short ‘Double water exclusion’: a hypothesis refining the O-ring theory for the hot spots at protein interfaces
title_sort ‘double water exclusion’: a hypothesis refining the o-ring theory for the hot spots at protein interfaces
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2654803/
https://www.ncbi.nlm.nih.gov/pubmed/19179356
http://dx.doi.org/10.1093/bioinformatics/btp058
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