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Science 26 July 1985:
Vol. 229. no. 4711, pp. 337 - 345
DOI: 10.1126/science.4012322

Articles

Science, Vol 229, Issue 4711, 337-345
Copyright © 1985 by American Association for the Advancement of Science


articles

Rate theories and puzzles of hemeprotein kinetics

H Frauenfelder and PG Wolynes

The binding of dioxygen and carbon monoxide to heme proteins such as myoglobin and hemoglobin has been studied with flash photolysis. At temperatures below 200 K, binding occurs from within the heme pocket and, contrary to expectation, with nearly equal rates for both ligands. This observation has led to a reexamination of the theory of the association reaction taking into account friction, protein structure, and the nature of electronic transitions. The rate coefficients for the limiting cases of large and small friction are found with simple arguments that use characteristic lengths and times. The arguments indicate how transition state theory as well as calculations based on nonadiabatic perturbation theory, which is called the Golden Rule, may fail. For ligand-binding reactions the data suggest the existence of intermediate states not directly observed so far. The general considerations may also apply to other biomolecular processes such as electron transport.


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