Using Capillary Electrophoresis to Investigate Protein Conformational and Compositional Heterogeneity

Abstract: Detailed insights into protein structure/function relationships require robust characterization methodologies. Free‐solution capillary electrophoresis (CE) is a unique separation technique which is sensitive to the conformation and/or composition of proteins, and therefore provides information on the heterogeneity of these properties. Three unrelated, conformationally/compositionally‐altered proteins were separated by CE. An electrophoretic mobility distribution was determined for each protein along with its conformational and/or compositional heterogeneity. The CE results were compared with molar mass distributions obtained from size‐exclusion chromatography coupled to light scattering (SEC‐MALS). Bovine serum albumin multimers and two monomeric species were separated, highlighting variations in conformational/compositional heterogeneity among the multimers. Analysis of yeast alcohol dehydrogenase resolved two monomeric conformers and various tetrameric species, illustrating the impact of zinc ion removal and disulfide bond reduction on the protein's heterogeneity. The apo (calcium‐free) and holo forms of bovine α‐lactalbumin were separated and differences in the species’ heterogeneity were measured; by contrast, the SEC‐MALS profiles were identical. Comparative analysis of these structurally unrelated proteins provided novel insights into the interplay between molar mass and conformational/compositional heterogeneity. Overall, this study expands the utility of CE by demonstrating its capacity to discern protein species and their heterogeneity, properties which are not readily accessible by other analytical techniques.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Using Capillary Electrophoresis to Investigate Protein Conformational and Compositional Heterogeneity ; day:16 ; month:05 ; year:2024 ; extent:12
ChemBioChem ; (16.05.2024) (gesamt 12)

Creator
Grosas, Aidan B.
Du Plessis, Mar‐dean
Thevarajah, Joel J.
Gaborieau, Marianne
Carver, John A.
Castignolles, Patrice

DOI
10.1002/cbic.202400108
URN
urn:nbn:de:101:1-2405171405546.729860375891
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
14.08.2025, 10:45 AM CEST

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Associated

  • Grosas, Aidan B.
  • Du Plessis, Mar‐dean
  • Thevarajah, Joel J.
  • Gaborieau, Marianne
  • Carver, John A.
  • Castignolles, Patrice

Other Objects (12)