| Literature DB >> 31667558 |
Tyler Mrozowich1, Donald J Winzor2, David J Scott3,4, Trushar R Patel5,6,7.
Abstract
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.Entities:
Keywords: Bovine serum albumin; Second virial coefficients; Small cosolute effects; Small-angle X-ray scattering; Thermodynamic nonideality
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Year: 2019 PMID: 31667558 DOI: 10.1007/s00249-019-01404-0
Source DB: PubMed Journal: Eur Biophys J ISSN: 0175-7571 Impact factor: 1.733