Histone deacetylases (HDACs) have
found intense interest as drug
targets for a variety of diseases, but there is disagreement about
basic aspects of the inhibition and mechanism of HDACs. QM/MM calculations
of HDAC8 including a large QM region provide a model that is consistent
with the available crystal structures and structure–activity
relationships of different HDAC inhibitors. The calculations support
a spontaneous proton transfer from a hydroxamic acid to an active
site histidine upon binding to the zinc. The role of the H142/D176
catalytic dyad as the general base of the reaction is elucidated.
The reasons for the disagreements between previous proposals are discussed.
The results provide detailed insights into the unique mechanism of
HDACs, including the role of the two catalytic dyads and function
of the potassium near the active site. They also have important implications
for the design of novel inhibitors for a number of HDACs such as the
class IIa HDACs.
The heteronuclear oxo-cluster [VPO4](•+) is generated via electrospray ionization and investigated with respect to both its electronic structure as well as its gas-phase reactivity toward small hydrocarbons, thus permitting a comparison to the well-known vanadium-oxide cation [V2O4](•+). As described in previous studies, the latter oxide exhibits no or just minor reactivity toward small hydrocarbons, such as CH4, C2H6, C3H8, n-C4H10, and C2H4, while substitution of one vanadium by a phosphorus atom yields the reactive [VPO4](•+) ion; the latter brings about oxidative dehydrogenation (ODH) of saturated hydrocarbons, e.g., propane and butane as well as oxygen-atom transfer (OAT) to unsaturated hydrocarbons, e.g. ethene, at thermal conditions. Further, the gas-phase structure of [VPO4](•+) is determined by IR photodissociation spectroscopy and compared to that of [V2O4](•+). DFT calculations help to elucidate the reaction mechanism. The results underline the crucial role of phosphorus in terms of C-H bond activation of hydrocarbons by mixed VPO clusters.
A remarkable visible-light-promoted photoredox catalytic methodology involved with amines and ecofriendly potassium thioacids for amide formation was uncovered. This approach can mimic the natural coenzyme acetyl-CoA to selectively acylate amines without affecting other functional groups such as alcohols, phenols, esters, among others. The developed strategy may hold great potential for a comprehensive display of biologically interesting peptide synthesis and amino acid modification through a diacyl disulfide intermediate.
Histone deacetylases (HDACs) emerged as important drug targets in epigenetics. The most common HDAC inhibitors use hydroxamic acids as zinc binding groups despite unfavorable pharmacokinetic properties. A two-stage protocol of M05-2X calculations of a library of 48 fragments in a small model active site, followed by QM/MM hybrid calculations of the full enzyme with selected binders is used to prospectively select potential bidentate zinc binders. The energetics and interaction patterns of several zinc binders not previously used for the inhibition of HDACs are discussed.
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