Abstract

Among the numerous contributions of Geoffrey Bodenhausen to NMR spectroscopy, his developments in the field of spin-relaxation methodology and theory will definitely have a long lasting impact. Starting with his seminal contributions to the excitation of multiple-quantum coherences, he and his group thoroughly investigated the intricate relaxation properties of these "forbidden fruits" and developed experimental techniques to reveal the relevance of previously largely ignored cross-correlated relaxation (CCR) effects, as "the essential is invisible to the eyes". Here we consider CCR within the challenging context of intrinsically disordered proteins (IDPs) and emphasize its potential and relevance for the studies of structural dynamics of IDPs in the future years to come. Conventionally, dynamics of globularly folded proteins are modeled and understood as deviations from otherwise rigid structures tumbling in solution. However, with increasing protein flexibility, as observed for IDPs, this apparent dichotomy between structure and dynamics becomes blurred. Although complex dynamics and ensemble averaging might impair the extraction of mechanistic details even further, spin relaxation uniquely encodes a protein's structural memory. Due to significant methodological developments, such as high-dimensional non-uniform sampling techniques, spin relaxation in IDPs can now be monitored in unprecedented resolution. Not embedded within a rigid globular fold, conventional spin probes might not suffice to capture the inherently local nature of IDP dynamics. To better describe and understand possible segmental motions of IDPs, we propose an experimental approach to detect the signature of anisotropic segmental dynamics by quantifying cross-correlated spin relaxation of individual and spin pairs. By adapting Geoffrey Bodenhausen's symmetrical reconversion principle to obtain zero frequency spectral density values, we can define and demonstrate more sensitive means to characterize anisotropic dynamics in IDPs.

Highlights

  • Geoffrey Bodenhausen’s 70th anniversary marks an ideal occasion to take a fresh look at some of his numerous contributions to spin-relaxation methodology and theory

  • An appropriate estimate for the average correlation time is an important prerequisite for the angular evaluation of cross-correlated relaxation (CCR) of remote spins (Kauffmann et al, 2021)

  • The fully anisotropic 13C chemical shift anisotropy (CSA) leads to spectral density contributions of two perpendicular components, it is subject to considerable variations (Markwick et al, 2005; Cisnetti et al, 2004; Loth et al, 2005)

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Summary

Introduction

Geoffrey Bodenhausen’s 70th anniversary marks an ideal occasion to take a fresh look at some of his numerous contributions to spin-relaxation methodology and theory. By considering his experiments within the challenging context of intrinsically disordered proteins (IDPs), we want to emphasize their potential and relevance in the future years to come. This rediscovery might require some collective effort, as current trends appear to point in the opposite direction.

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