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High pressure reveals structural determinants for globin hexacoordination: Neuroglobin and myoglobin cases
Author(s) -
Capece L.,
Marti M. A.,
BidonChanal A.,
Nadra A.,
Luque F. J.,
Estrin D. A.
Publication year - 2009
Publication title -
proteins: structure, function, and bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.699
H-Index - 191
eISSN - 1097-0134
pISSN - 0887-3585
DOI - 10.1002/prot.22297
Subject(s) - neuroglobin , myoglobin , globin , molecular dynamics , biophysics , chemistry , high pressure , hemoglobin , biochemistry , biology , thermodynamics , computational chemistry , physics
The influence of pressure on the equilibrium between five‐(5c) and six‐coordination (6c) forms in neuroglobin (Ngb) and myoglobin (Mb) has been examined by means of molecular dynamics (MD) simulations at normal and high pressure. The results show that the main effect of high pressure is to reduce the protein mobility without altering the structure in a significant manner. Moreover, our data suggest that the equilibrium between 5c and 6c states in globins is largely controlled by the structure and dynamics of the C‐D region. Finally, in agreement with the available experimental data, the free energy profiles obtained from steered MD for both proteins indicate that high pressure enhances hexacoordination. In Ngb, the shift in equilibrium is mainly related to an increase in the 6c→5c transition barrier, whereas in Mb such a shift is primarily due to a destabilization of the 5c state. Proteins 2009. © 2008 Wiley‐Liss, Inc.