Determination of protein charge by capillary zone electrophoresis


Autoria(s): Winzor, D. J.; Jones, S.; Harding, S. E.
Data(s)

01/01/2004

Resumo

The feasibility of employing classical electrophoresis theory to determine the net charge (valence) of proteins by capillary zone electrophoresis is illustrated in this paper. An outline of a procedure to facilitate the interpretation of mobility measurements is demonstrated by its application to a published mobility measurement for Staphylococcal nuclease at pH 8.9 that had been obtained by capillary zone electrophoresis. The significantly higher valence of +7.5 (cf. 5.6 from the same series of measurements) that has been reported on the basis of a charge ladder approach for charge determination signifies the likelihood that the latter generic approach may be prone to error arising from nonconformity of the experimental system with an inherent assumption that chemical modification or mutation of amino acid residues has no effect on the overall three-dimensional size and shape of the protein. (C) 2004 Elsevier Inc. All rights reserved.

Identificador

http://espace.library.uq.edu.au/view/UQ:71030

Idioma(s)

eng

Publicador

Academic Press

Palavras-Chave #Biochemical Research Methods #Biochemistry & Molecular Biology #Chemistry, Analytical #Capillary Zone Electrophoresis #Mobility-charge Relationship #Protein Charge #Staphylococcal Nuclease #Solute Self-association #Gel-filtration #Sedimentation Equilibrium #Thermodynamic Nonideality #Molecular Weights #Consequences #Sephadex #Nuclease #Valence #C1 #270101 Analytical Biochemistry #780105 Biological sciences
Tipo

Journal Article