Tuning the attempt frequency of protein folding dynamics via transition-state rigidification: Application to Trp-cage

Abstract

The attempt frequency or prefactor (k0) of the transitionstate rate equation of protein folding kinetics has been estimated to be on the order of 106 s-1, which is many orders of magnitude smaller than that of chemical reactions. Herein we use the mini-protein Trp-cage to show that it is possible to significantly increase the value of k0 for a protein folding reaction by rigidifying the transition state. This is achieved by reducing the conformational flexibility of a key structural element (i.e., an α-helix) formed in the transition state via photo-isomerization of an azobenzene cross-linker. We find that this strategy not only decreases the folding time of the Trp-cage peptide by more than an order of magnitude (to ∼100 ns at 25°C) but also exposes parallel folding pathways, allowing us to provide, to the best of our knowledge, the first quantitative assessment of the curvature of the transition-state free-energy surface of a protein. (Figure Presented).