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Low temperature study of myoglobin-ligand rebinding kinetics with Mössbauer spectroscopy

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Abstract

We have studied the recombination kinetics of carboxymyoglobin (after photodissociation of the CO ligand) by Mössbauer spectroscopy for temperatures in the range 4.2 – 60 K. The observed kinetics display non-exponential behaviour which was monitored over periods of a few days. It is shown that the time dependence of the kinetics can be reduced to a single universal function of the temperature-dependent variable (t/τ 1/2(T))β(T). The half-decay time τ 1/2(T) and the scaling parameter β(T) are analysed for the presence of tunneling effects. The non-Arrhenius temperature dependence of the half-decay time below 60 K is interpreted as activated tunneling in models with an Eckart barrier or a fluctuating barrier.

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Received: 19 November 1996 / Accepted: 17 March 1997

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Ober, C., Burkardt, M., Winkler, H. et al. Low temperature study of myoglobin-ligand rebinding kinetics with Mössbauer spectroscopy. Eur Biophys J 26, 227–237 (1997). https://doi.org/10.1007/s002490050075

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  • DOI: https://doi.org/10.1007/s002490050075

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