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Protein Science (2008), 17:216-227. Published by Cold Spring Harbor Laboratory Press. Copyright © 2008 The Protein Society
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Electrostatic effects in unfolded staphylococcal nuclease

Nicholas C. Fitzkee and Bertrand García-Moreno E

Department of Biophysics, Johns Hopkins University, Baltimore, Maryland 21218, USA

(RECEIVED June 18, 2007; FINAL REVISION October 6, 2007; ACCEPTED October 31, 2007)

Structure-based calculations of pK a values and electrostatic free energies of proteins assume that electrostatic effects in the unfolded state are negligible. In light of experimental evidence showing that this assumption is invalid for many proteins, and with increasing awareness that the unfolded state is more structured and compact than previously thought, a detailed examination of electrostatic effects in unfolded proteins is warranted. Here we address this issue with structure-based calculations of electrostatic interactions in unfolded staphylococcal nuclease. The approach involves the generation of ensembles of structures representing the unfolded state, and calculation of Coulomb energies to Boltzmann weight the unfolded state ensembles. Four different structural models of the unfolded state were tested. Experimental proton binding data measured with a variant of nuclease that is unfolded under native conditions were used to establish the validity of the calculations. These calculations suggest that weak Coulomb interactions are an unavoidable property of unfolded proteins. At neutral pH, the interactions are too weak to organize the unfolded state; however, at extreme pH values, where the protein has a significant net charge, the combined action of a large number of weak repulsive interactions can lead to the expansion of the unfolded state. The calculated pK a values of ionizable groups in the unfolded state are similar but not identical to the values in small peptides in water. These studies suggest that the accuracy of structure-based calculations of electrostatic contributions to stability cannot be improved unless electrostatic effects in the unfolded state are calculated explicitly.

Keywords: proteins electrostatics; unfolded state; staphylococcal nuclease; pK a values


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