The Transition State of Coupled Folding and Binding for a Flexible β-Finger

Flexible and fully disordered protein regions that fold upon binding mediate numerous protein–protein interactions. However, little is known about their mechanism of interaction. One such coupled folding and binding occurs when a flexible region of neuronal nitric oxide synthase adopts a β-finger structure upon binding to its protein ligand, a PDZ [PSD-95 (postsynaptic density protein-95)/Discs large/ZO-1] domain from PSD-95. We have analyzed this binding reaction by protein engineering combined with kinetic experiments. Mutational destabilization of the β-finger changed mainly the dissociation rate constant of the proteins and, to a lesser extent, the association rate constant. Thus, mutation affected late events in the coupled folding and binding reaction. Our results therefore suggest that the native binding interactions of the β-finger are not present in the rate-limiting transition state for binding but form on the downhill side in a cooperative manner. However, by mutation, we could destabilize the β-finger further and change the rate-limiting step such that an initial conformational change becomes rate limiting. This switch in rate-limiting step shows that multistep binding mechanisms are likely to be found among flexible and intrinsically disordered regions of proteins. [Display omitted] ► The coupled folding and binding reaction of a flexible β-finger was studied by kinetics and mutagenesis. ► Native binding interactions of the β-finger are formed after the rate-limiting transition state for binding in a cooperative manner. ► One particular point mutation makes a slow conformational change rate limiting. ► Results are consistent with previous model for binding of disordered peptides.