Time Resolved EPR Study on the Photoinduced Long-Range Charge-Separated State in Protein: Electron Tunneling Mediated by Arginine Residue in Human Serum Albumin (original) (raw)

The journal of physical chemistry. B, 2016

Abstract

To elucidate how local molecular conformations play a role on electronic couplings for the long-range photoinduced charge-separated (CS) states in protein systems, we have analyzed time-resolved electron paramagnetic resonance (TREPR) spectra by polarized laser irradiations of 9,10-anthraquinone-1-sulfonate (AQ1S(-)) bound to human serum albumin (HSA). Analyses of the magnetophotoselection effects on the EPR spectra and a docking simulation clarified the molecular geometry and the electronic coupling of the long-range CS states of AQ1S(•2-)-tryptophan214 radical cation (W214(•+)) separated by 1.2 nm. The ligand of AQ1S(-) has been demonstrated to be bound to the drug site I in HSA. Molecular conformations of the binding region were estimated by the docking simulations, indicating that an arginine218 (R218(+)) residue bound to AQ1S(•2-) mediates the long-range electron-transfer. The energetics of triad states of AQ1S(•2-)-R218(+)-W214(•+) and AQ1S(-)-R218(•)-W214(•+) have been comput...

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