Related Experiment Video
Updated: Sep 23, 2026

NMR 15N Relaxation Experiments for the Investigation of Picosecond to Nanoseconds Structural Dynamics of Proteins
Published on: November 1, 2024
Invisible but not inaccessible-Revealing transient oligomers formed by intrinsically disordered proteins with
1Laboratory of Chemical Physics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.
Abstract:
Intrinsically disordered proteins (IDPs) are often readily characterized as soluble monomers, whereas their biological and pathological roles frequently involve transient, heterogeneous, or sparsely populated oligomers. Such assemblies are often described as 'invisible' but invisibility is method-dependent: Oligomers that escape direct detection by one technique may remain accessible through indirect or complementary measurements. Solution NMR is uniquely positioned to exploit exchange between observable monomers and NMR-invisible oligomers, providing residue-specific information on populations, kinetics, and intermolecular contacts. Other methods report on mass, stoichiometry, dimensions, morphology, or site-specific distance distributions. Here, we discuss how integrating orthogonal measurements can overcome method-specific blind spots and yield a self-consistent model that simultaneously accounts for structure, populations, exchange kinetics, and morphology, something no single method can provide.
Related Concept Videos
¹H NMR: Interpreting Distorted and Overlapping Signals
As Δν decreases and the signals move closer, the doublets appear increasingly distorted. The intensities of the inner lines increase at the cost of those of the outer lines as the signals are slanted or...
Intrinsically Disordered Proteins
¹H NMR of Conformationally Flexible Molecules: Temporal Resolution
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)
¹H NMR of Conformationally Flexible Molecules: Variable-Temperature NMR

