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Experimental determination of second virial coefficients by small-angle X-ray scattering: a problem revisited.
Mrozowich, Tyler; Winzor, Donald J; Scott, David J; Patel, Trushar R.
Afiliación
  • Mrozowich T; Department of Chemistry and Biochemistry, Alberta RNA Research and Training Institute, University of Lethbridge, 4401 University Drive, Lethbridge, AB, T1K 3M4, Canada.
  • Winzor DJ; School of Chemistry and Molecular Biosciences, University of Queensland, Brisbane, QLD, 4072, Australia.
  • Scott DJ; National Centre for Macromolecular Hydrodynamics, School of Biosciences, University of Nottingham, Sutton Bonington Campus, Nottingham, LE12 5RD, UK. david.scott@nottingham.ac.uk.
  • Patel TR; ISIS Spallation Neutron and Muon Source, Rutherton Appleton Research Complex at Harwell, Harwell, OX11 OFA, UK. david.scott@nottingham.ac.uk.
Eur Biophys J ; 48(8): 781-787, 2019 Dec.
Article en En | MEDLINE | ID: mdl-31667558
This investigation examines the validity of employing single-solute theory to interpret SAXS measurements on buffered protein solutions-the current practice despite the necessity to regard the buffer components as additional non-scattering solutes rather than as part of the solvent. The present study of bovine serum albumin in phosphate-buffered saline supplemented with 20-100 g/L sucrose as small cosolute has certainly verified the prediction that the experimentally obtained second virial coefficient should contain protein-cosolute contributions. Nevertheless, the second virial coefficient determined for protein solutions supplemented with high cosolute concentrations on the basis of single-solute theory remains a valid means for identifying conditions conducive to protein crystallization, because the return of a slightly negative second virial coefficient based on single-solute theory [Formula: see text] still establishes the existence of slightly associative interactions between protein molecules, irrespective of the molecular source-protein self-interactions and/or protein-cosolute contributions.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Difracción de Rayos X / Dispersión del Ángulo Pequeño Límite: Animals Idioma: En Revista: Eur Biophys J Asunto de la revista: BIOFISICA Año: 2019 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Difracción de Rayos X / Dispersión del Ángulo Pequeño Límite: Animals Idioma: En Revista: Eur Biophys J Asunto de la revista: BIOFISICA Año: 2019 Tipo del documento: Article País de afiliación: Canadá