Structural features of [NiFeSe] and [NiFe] hydrogenases determining their different properties: a computational approach

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Hydrogenases are metalloenzymes that catalyze the reversible reaction H-2 reversible arrow 2H(+) + 2e(-), being potentially useful in H-2 production or oxidation. [NiFeSe] hydrogenases are a particularly interesting subgroup of the [NiFe] class that exhibit tolerance to O-2 inhibition and produce more H-2 than standard [NiFe] hydrogenases. However, the molecular determinants responsible for these properties remain unknown. Hydrophobic pathways for H-2 diffusion have been identified in [NiFe] hydrogenases, as have proton transfer pathways, but they have never been studied in [NiFeSe] hydrogenases. Our aim was, for the first time, to characterize the H-2 and proton pathways in a [NiFeSe] hydrogenase and compare them with those in a standard [NiFe] hydrogenase. We performed molecular dynamics simulations of H-2 diffusion in the [NiFeSe] hydrogenase from Desulfomicrobium baculatum and extended previous simulations of the [NiFe] hydrogenase from Desulfovibrio gigas (Teixeira et al. in Biophys J 91:2035-2045, 2006). The comparison showed that H-2 density near the active site is much higher in [NiFeSe] hydrogenase, which appears to have an alternative route for the access of H-2 to the active site. We have also determined a possible proton transfer pathway in the [NiFeSe] hydrogenase from D. baculatum using continuum electrostatics and Monte Carlo simulation and compared it with the proton pathway we found in the [NiFe] hydrogenase from D. gigas (Teixeira et al. in Proteins 70:1010-1022, 2008). The residues constituting both proton transfer pathways are considerably different, although in the same region of the protein. These results support the hypothesis that some of the special properties of [NiFeSe] hydrogenases could be related to differences in the H-2 and proton pathways.
Original languageUnknown
Pages (from-to)543-555
JournalJournal Of Biological Inorganic Chemistry
Issue number4
Publication statusPublished - 1 Jan 2012

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