Static solid-state 2H NMR methods in studies of protein side-chain dynamics

Prog Nucl Magn Reson Spectrosc. 2017 Aug:101:1-17. doi: 10.1016/j.pnmrs.2017.02.001. Epub 2017 Mar 14.

Abstract

In this review, we discuss the experimental static deuteron NMR techniques and computational approaches most useful for the investigation of side-chain dynamics in protein systems. Focus is placed on the interpretation of line shape and relaxation data within the framework of motional modeling. We consider both jump and diffusion models and apply them to uncover glassy behaviors, conformational exchange and dynamical transitions in proteins. Applications are chosen from globular and membrane proteins, amyloid fibrils, peptide adsorbed on surfaces and proteins specific to connective tissues.

Keywords: Dynamical transitions; Protein dynamics; Solid-state NMR; Static deuteron NMR.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Deuterium
  • Magnetic Resonance Spectroscopy / methods*
  • Peptides / chemistry
  • Protein Conformation
  • Proteins / chemistry*

Substances

  • Peptides
  • Proteins
  • Deuterium