Literature DB >> 17266122

X-ray absorption and molecular dynamics study of cation binding sites in the purple membrane.

Francesc Sepulcre1, Arnau Cordomí, M Grazia Proietti, Juan J Perez, Joaquin García, Enric Querol, Esteve Padrós.   

Abstract

The present work describes the results of a study aimed at identifying candidate cation binding sites on the extracellular region of bacteriorhodopsin, including a site near the retinal pocket. The approach used is a combined effort involving computational chemistry methods (computation of cation affinity maps and molecular dynamics) together with the Extended X-Ray Absorption Fine Structure (EXAFS) technique to obtain relevant information about the local structure of the protein in the neighborhood of Mn(2+) ions in different affinity binding sites. The results permit the identification of a high-affinity binding site where the ion is coordinated simultaneously to Asp212(-) and Asp85(-). Comparison of EXAFS data of the wild type protein with the quadruple mutant E9Q/E74Q/E194Q/E204Q at pH 7.0 and 10.0 demonstrate that extracellular glutamic acid residues are involved in cation binding. (c) 2007 Wiley-Liss, Inc.

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Year:  2007        PMID: 17266122     DOI: 10.1002/prot.21273

Source DB:  PubMed          Journal:  Proteins        ISSN: 0887-3585


  1 in total

1.  Combination of extended X-ray absorption fine structure spectroscopy with lipidic cubic phases for the study of cation binding in bacteriorhodopsin.

Authors:  Alex Perálvarez-Marín; Francesc Sepulcre; Mercedes Márquez; Maria Grazia Proietti; Esteve Padrós
Journal:  Eur Biophys J       Date:  2011-06-12       Impact factor: 1.733

  1 in total

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