Publication | Closed Access
Tunneling in Ligand Binding to Heme Proteins
131
Citations
15
References
1976
Year
EngineeringMolecular BiologyExcitation Energy TransferLigand BindingHeme TraffickingTunneling MicroscopyBarrier HeightProtein FoldingPhotophysical PropertyBiophysicsQuantum ScienceBiochemistryPhysicsHeme SignalingAtomic PhysicsHeme TransportPhysical ChemistryQuantum ChemistryTunneling RateLaser PhotochemistryNatural SciencesSpectroscopyApplied PhysicsQuantum BiologyCarbon Monoxide
Rebinding of carbon monoxide to the beta chain of hemoglobin after photodissociation by a laser flash is intramolecular below about 200 K. Above 25 K, rebinding occurs via classical over-the-barrier motion; below, quantum-mechanical tunneling dominates. Both are described by an energy spectrum peaked at Epeak=4.0 kilojoules per mole. The barrier width d(E), determined from the energy dependence of the tunneling rate, depends on barrier height, d(E) approximately 0.05 nanometer X (E/Epeak) 1.5.
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