Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/62426
Title: Role of PheE15 gate in ligand entry and nitric oxide detoxification function of Mycobacterium tuberculosis truncated hemoglobin N
Author: Oliveira, Ana
Singh, Sandeep
Bidon-Chanal Badia, Axel
Forti, Flavio
Martí, Marcelo A.
Boechi, Leonardo
Estrin, Darío
Dikshit, Kanak L.
Luque Garriga, F. Xavier
Keywords: Mycobacterium tuberculosis
Òxid nítric
Proteïnes
Bacteris
Hemoglobina
Mycobacterium tuberculosis
Nitric oxide
Proteins
Bacteria
Hemoglobin
Issue Date: 8-Nov-2012
Publisher: Public Library of Science (PLoS)
Abstract: The truncated hemoglobin N, HbN, of Mycobacterium tuberculosis is endowed with a potent nitric oxide dioxygenase (NOD) activity that allows it to relieve nitrosative stress and enhance in vivo survival of its host. Despite its small size, the protein matrix of HbN hosts a two-branched tunnel, consisting of orthogonal short and long channels, that connects the heme active site to the protein surface. A novel dual-path mechanism has been suggested to drive migration of O(2) and NO to the distal heme cavity. While oxygen migrates mainly by the short path, a ligand-induced conformational change regulates opening of the long tunnel branch for NO, via a phenylalanine (PheE15) residue that acts as a gate. Site-directed mutagenesis and molecular simulations have been used to examine the gating role played by PheE15 in modulating the NOD function of HbN. Mutants carrying replacement of PheE15 with alanine, isoleucine, tyrosine and tryptophan have similar O(2)/CO association kinetics, but display significant reduction in their NOD function. Molecular simulations substantiated that mutation at the PheE15 gate confers significant changes in the long tunnel, and therefore may affect the migration of ligands. These results support the pivotal role of PheE15 gate in modulating the diffusion of NO via the long tunnel branch in the oxygenated protein, and hence the NOD function of HbN.
Note: Reproducció del document publicat a: http://dx.doi.org/10.1371/journal.pone.0049291
It is part of: PLoS One, 2012, vol. 7, num. 11, p. e49291
Related resource: http://dx.doi.org/10.1371/journal.pone.0049291
URI: http://hdl.handle.net/2445/62426
ISSN: 1932-6203
Appears in Collections:Articles publicats en revistes (Farmàcia, Tecnologia Farmacèutica i Fisicoquímica)
Articles publicats en revistes (Institut de Biomedicina (IBUB))

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