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Updated: Jul 16, 2026

NMR 15N Relaxation Experiments for the Investigation of Picosecond to Nanoseconds Structural Dynamics of Proteins
Published on: November 1, 2024
Probe-dependent and nonexponential relaxation kinetics: unreliable signatures of downhill protein folding
1Department of Physics, University of Florida, Gainesville, Florida 32611-8440, USA. sjhagen@ufl.edu
Abstract:
The theoretical suggestion that some proteins may encounter no significant free energy barriers during their folding raises an important question: What experimental signature does this downhill folding produce? Several authors have argued that nonexponential (and especially stretched exponential) or probe-dependent kinetics represent useful experimental signatures of a downhill free energy surface. Here we examine more closely the connection between unusual kinetics and downhill energy surfaces. Simulation of diffusive relaxation dynamics on a variety of generically downhill, two-dimensional free energy surfaces shows that these surfaces do not necessarily produce either probe-dependent or significantly nonexponential kinetics. Conversely, we find that two-dimensional surfaces with significant (>3 k(B) T) energy barriers can readily give rise to nonexponential and probe-dependent kinetics. These results show that downhill folding does not constitute a necessary or sufficient condition for nonexponential and/or probe-dependent folding kinetics. One cannot easily prove or disprove that a protein folds downhill simply by studying its relaxation kinetics.
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