Tunneling in Ligand Binding to Heme Proteins

N. Alberding(University of Illinois Urbana-Champaign), Robert H. Austin(University of Illinois Urbana-Champaign), K. W. Beeson(University of Illinois Urbana-Champaign), S. S. Chan(University of Illinois Urbana-Champaign), L. Eisenstein(University of Illinois Urbana-Champaign), Hans Frauenfelder(University of Illinois Urbana-Champaign), T. M. Nordlund(University of Illinois Urbana-Champaign)
Science
June 4, 1976
Cited by 131

Abstract

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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