Collective NMR relaxation model applied to protein dynamics

Rafael Brüschweiler and David A. Case
Phys. Rev. Lett. 72, 940 – Published 7 February 1994
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Abstract

A new dynamical model for the interpretation of nuclear magnetic resonance relaxation data is presented. It is based on a normal mode description, treating the low frequencies associated with collective motions as adjustable parameters to optimize agreement between calculated and experimental relaxation order parameters. This model provides a compact representation of many aspects of internal dynamics and characterizes motions affecting different spin pairs in a correlated way. Furthermore, it links together dynamical characteristics of different types of NMR observables and allows one to assess vibrational thermodynamic properties. Sample applications are given for a 25-residue zinc-finger peptide.

  • Received 6 July 1993

DOI:https://doi.org/10.1103/PhysRevLett.72.940

©1994 American Physical Society

Authors & Affiliations

Rafael Brüschweiler and David A. Case

  • Department of Molecular Biology, The Scripps Research Institute, LaJolla, California 92037

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Vol. 72, Iss. 6 — 7 February 1994

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