Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/74772
Title: Hydrogen bonding effect between active site and protein environment on catalysis performance in H2-producing [NiFe] hydrogenases
Authors: Qiu, Siyao
Azofra Mesa, Luis Miguel 
MacFarlane, Douglas R.
Sun, Chenghua
UNESCO Clasification: 221001 Catálisis
Issue Date: 2018
Journal: Physical Chemistry Chemical Physics 
Abstract: The interaction between the active site and the surrounding protein environment plays a fundamental role in the hydrogen evolution reaction (HER) in [NiFe] hydrogenases. Our density functional theory (DFT) findings demonstrate that the reaction Gibbs free energy required for the rate determining step decreases by 7.1 kcal mol1 when the surrounding protein environment is taken into account, which is chiefly due to free energy decreases for the two H+/e addition steps (the so-called Ni-SIa to I1, and Ni-C to Ni-R), being the largest thermodynamic impediments of the whole reaction. The variety of hydrogen bonds (H-bonds) between the amino acids and the active site is hypothesised to be the main reason for such stability: H-bonds not only work as electrostatic attractive forces that influence the charge redistribution, but more importantly, they act as an electron ‘pull’ taking electrons from the active site towards the amino acids. Moreover, the electron ‘pull’ effect through H-bonds via the S in cysteine residues shows a larger influence on the energy profile than that via the CN ligands on Fe.
URI: http://hdl.handle.net/10553/74772
ISSN: 1463-9076
DOI: 10.1039/C7CP07685A
Source: Physical chemistry chemical physics [ISSN 1463-9076], v. 20, p. 6735-6743
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