The Vroman effect: Competitive protein exchange with dynamic multilayer protein aggregates

• Published in: Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2013-03, Vol.103, p.395-404
• Main Authors: Hirsh, Stacey L., McKenzie, David R., Nosworthy, Neil J., Denman, John A., Sezerman, Osman U., Bilek, Marcela M.M.
• Format: Article
• Language: English
• Subjects: Adsorption; Atomic force microscopy; binding capacity; biofouling; bioreactors; Cellulase; Cellulase - chemistry; Cellulase - metabolism; colloids; disease diagnosis; endo-1,4-beta-glucanase; food processing; Isoelectric Point; Mass Spectrometry; medical equipment; Microscopy, Atomic Force; Models, Biological; Molecular Weight; Polystyrenes - chemistry; Principal Component Analysis; protein aggregates; protein composition; Protein immobilization; Protein Structure, Quaternary; Proteins - chemistry; Proteins - metabolism; Time Factors; Trypsin - metabolism; Vroman effect
• ISSN: 0927-7765; 1873-4367
• DOI: 10.1016/j.colsurfb.2012.10.039

[Display omitted] ► We establish that competitive protein exchange on surfaces (“Vroman effect”) can occur through the turning of multilayer protein aggregates. ► We show that adsorption of a cellulase enzyme mixture onto polystyrene results in multilayer protein aggregates and competitive protein exchange. ► Experimental evidence from AFM, QCM-D, TOF-SIMS, and in-solution TOF-MS is obtained and interpreted in terms of a model for the kinetics and competitive behavior of adsorption from protein mixtures. The surface immobilization of proteins is an emerging field with applications in a wide range of important areas: biomedical devices, disease diagnosis, biosensing, food processing, biofouling, and bioreactors. Proteins, in Nature, often work synergistically, as in the important enzyme mixture, cellulase. It is necessary to preserve these synergies when utilizing surface immobilized proteins. However, the competitive displacement of earlier adsorbed proteins by other proteins with stronger binding affinities (the “Vroman effect”) results in undesired layer instabilities that are difficult to control. Although this nanoscale phenomenon has been extensively studied over the last 40 years, the process through which this competitive exchange occurs is not well understood. This paper uses atomic force microscopy, QCM-D, TOF-SIMS, and in-solution TOF-MS to show that this competitive exchange process can occur through the turning of multilayer protein aggregates. This dynamic process is consistent with earlier postulated “transient complex” models, in which the exchange occurs in three stages: an initial layer adsorbs, another protein layer then embeds itself into the initial layer, forming a “transient complex;” the complex “turns,” exposing the first layer to solution; proteins from the first layer desorb resulting in a final adsorbed protein composition that is enriched in proteins from the second layer.