Assessment of protein reorientational diffusion in solution by 13C off-resonance rotating frame spin-lattice relaxation: effect of polydispersity

Biopolymers. 1990 Feb 15;29(3):501-7. doi: 10.1002/bip.360290305.

Abstract

The 13C off-resonance rotating frame spin-lattice relaxation technique is applicable to the study of protein rotational diffusion behavior in both model in vitro and in vivo systems. The original formalism of James and co-workers [(1978) J. Am. Chem. Soc. 100, 3590-3594] was constrained by the assumption of random isotropic reorientational motion of a monodisperse protein population. Here we extend the formalism to include polydispersity. Application is made to the alkaline pH induced association of lysozyme, lysozyme-bovine serum albumin mixtures, and to the phase separation of lysozyme salt-water mixtures induced by low temperature.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Carbon Isotopes
  • Diffusion
  • Hydrogen-Ion Concentration
  • Magnetic Resonance Spectroscopy / methods
  • Models, Biological
  • Muramidase
  • Protein Conformation
  • Proteins*
  • Serum Albumin, Bovine
  • Solutions

Substances

  • Carbon Isotopes
  • Proteins
  • Solutions
  • Serum Albumin, Bovine
  • Muramidase