Please use this identifier to cite or link to this item: https://ktisis.cut.ac.cy/handle/10488/6545
Title: Binding and docking interactions of NO, CO and O 2 in heme proteins as probed by density functional theory
Authors: Varotsis, Constantinos 
Daskalakis, Evangelos 
Keywords: Density functionals;Carbon monoxide;Hemoproteins;Nitric oxide;Oxygen;Hydrogen bonding;Molecular dynamics;Protein binding
Issue Date: 2009
Publisher: MDPI
Source: International journal of molecular sciences, 2009, volume 10, issue 9, pages 4137-4156
Abstract: Dynamics and reactivity in heme proteins include direct and indirect interactions of the ligands/substrates like CO, NO and O 2 with the environment. Direct electrostatic interactions result from amino acid side chains in the inner cavities and/or metal coordination in the active site, whereas indirect interactions result by ligands in the same coordination sphere. Interactions play a crucial role in stabilizing transition states in catalysis or altering ligation chemistry. We have probed, by Density Functional Theory (DFT), the perturbation degree in the stretching vibrational frequencies of CO, NO and O 2 molecules in the presence of electrostatic interactions or hydrogen bonds, under conditions simulating the inner cavities. Moreover, we have studied the vibrational characteristics of the heme bound form of the CO and NO ligands by altering the chemistry of the proximal to the heme ligand. CO, NO and O 2 molecules are highly polarizable exerting vibrational shifts up to 80, 200 and 120 cm -1, respectively, compared to the non-interacting ligand. The importance of Density Functional Theory (DFT) methodology in the investigation of the heme-ligand-protein interactions is also addressed
URI: http://ktisis.cut.ac.cy/handle/10488/6545
ISSN: 14220067
DOI: 10.3390/ijms10094137
Rights: © 2009 by the authors
Type: Article
Appears in Collections:Άρθρα/Articles

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