Back to Search Start Over

Shedding light on protein–ligand binding by graph theory: The topological nature of allostery

Authors :
De Ruvo, Micol
Giuliani, Alessandro
Paci, Paola
Santoni, Daniele
Di Paola, Luisa
Source :
Biophysical Chemistry. May2012, Vol. 165/166, p21-29. 9p.
Publication Year :
2012

Abstract

Abstract: Allostery is a very important feature of proteins; we propose a mesoscopic approach to allosteric mechanisms elucidation, based on protein contact matrices. The application of graph theory methods to the characterization of the allosteric process and, more broadly, to obtain the conformational changes upon binding, reveals key features of the protein function. The proposed method highlights the leading role played by topological over geometrical changes in allosteric transitions. Topological invariants were able to discriminate between true allosteric motions and generic protein motions upon binding. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
03014622
Volume :
165/166
Database :
Academic Search Index
Journal :
Biophysical Chemistry
Publication Type :
Academic Journal
Accession number :
75183999
Full Text :
https://doi.org/10.1016/j.bpc.2012.03.001