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[Fe‐Fe]‐hydrogenase reactivated by residue mutations as bridging carbonyl rearranges: A QM/MM study
Author(s) -
Motiu Stefan,
Gogonea Valentin
Publication year - 2010
Publication title -
international journal of quantum chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.484
H-Index - 105
eISSN - 1097-461X
pISSN - 0020-7608
DOI - 10.1002/qua.22381
Subject(s) - chemistry , oniom , qm/mm , gibbs free energy , hydrogenase , ab initio , residue (chemistry) , active site , enzyme , stereochemistry , crystallography , catalysis , computational chemistry , molecular dynamics , thermodynamics , organic chemistry , physics
In this work, we found aqueous enzyme phase reaction pathways for the reactivation of the exogenously inhibited [Fe‐Fe]‐hydrogenases by O 2 , or OH − , which metabolizes to H 2 O (Dogaru et al., Int J Quantum Chem 2008, 108; Motiu et al., Int J Quantum Chem 2007, 107, 1248). We used the hybrid quantum mechanics/molecular mechanics (QM/MM) method to study the reactivation pathways of the exogenously inhibited enzyme matrix. The ONIOM calculations performed on the enzyme agree with experimental results (Liu et al., J Am Chem Soc 2002, 124, 5175), that is, wild‐type [Fe‐Fe]‐hydrogenase H‐cluster is inhibited by oxygen metabolites. An enzyme spherical region with a radius of 8 Å (from the distal iron, Fe d ) has been screened for residues that prevent H 2 O from leaving the catalytic site and reactivate the [Fe‐Fe]‐hydrogenase H‐cluster. In the screening process, polar residues were removed, one at a time, and frequency calculations provided the change in the Gibbs' energy for the dissociation of water (due to their deletion). When residue deletion resulted in significant Gibbs' energy decrease, further residue substitutions have been carried out. Following each substitution, geometry optimization and frequency calculations have been performed to assess the change in the Gibbs' energy for the elimination of H 2 O. Favorable thermodynamic results have been obtained for both single residue removal (Δ G ΔGlu 374 = −1.6 kcal/mol), single substitution (Δ G Glu 374 His = −3.1 kcal/mol), and combined residue substitutions (Δ G Arg 111 Glu;Thr 145 Val;Glu 374 His;Tyr 375 Phe = −7.5 kcal/mol). Because the wild‐type enzyme has only an endergonic step to overcome, that is, for H 2 O removal, by eliminating several residues, one at a time, the endergonic step was made to proceed spontaneously. Thus, the most promising residue deletions which enhance H 2 O elimination are ΔArg 111 , ΔThr 145 , ΔSer 177 , ΔGlu 240 , ΔGlu 374 , and ΔTyr 375 . The thermodynamics and electronic structure analyses show that the bridging carbonyl (CO b ) of the H‐cluster plays a concomitant role in the enzyme inhibition/reactivation. In gas phase, CO b shifts towards Fe d to compensate for the electron density donated to oxygen upon the elimination of H 2 O. However, this is not possible in the wild‐type enzyme because the protein matrix hinders the displacement of CO b towards Fe d , which leads to enzyme inhibition. Nevertheless, enzyme reactivation can be achieved by means of appropriate amino acid substitutions. © 2009 Wiley Periodicals, Inc. Int J Quantum Chem, 2010