Combining An Optical Resonance Biosensor With Enzyme Activity Kinetics To Understand Protein Adsorption And Denaturation
Keywords
Biosensor; Modeling; Nanobiotechnology; Protein adsorption; Self-assembled monolayer; Surface modification
Abstract
Understanding protein adsorption and resultant conformation changes on modified and unmodified silicon dioxide surfaces is a subject of keen interest in biosensors, microfluidic systems and for medical diagnostics. However, it has been proven difficult to investigate the kinetics of the adsorption process on these surfaces as well as understand the topic of the denaturation of proteins and its effect on enzyme activity. A highly sensitive optical whispering gallery mode (WGM) resonator was used to study a catalytic enzyme's adsorption processes on different silane modified glass substrates (plain glass control, DETA, 13F, and SiPEG). The WGM sensor was able to obtain high resolution kinetic data of glucose oxidase (GO) adsorption with sensitivity of adsorption better than that possible with SPR. The kinetic data, in combination with a functional assay of the enzyme activity, was used to test hypotheses on adsorption mechanisms. By fitting numerical models to the WGM sensograms for protein adsorption, and by confirming numerical predictions of enzyme activity in a separate assay, we were able to identify mechanisms for GO adsorption on different alkylsilanes and infer information about the adsorption of protein on nanostructured surfaces.
Publication Date
1-1-2015
Publication Title
Biomaterials
Volume
38
Number of Pages
86-96
Document Type
Article
Personal Identifier
scopus
DOI Link
https://doi.org/10.1016/j.biomaterials.2014.10.002
Copyright Status
Unknown
Socpus ID
84912141054 (Scopus)
Source API URL
https://api.elsevier.com/content/abstract/scopus_id/84912141054
STARS Citation
Wilson, Kerry A.; Finch, Craig A.; Anderson, Phillip; Vollmer, Frank; and Hickman, James J., "Combining An Optical Resonance Biosensor With Enzyme Activity Kinetics To Understand Protein Adsorption And Denaturation" (2015). Scopus Export 2015-2019. 1197.
https://stars.library.ucf.edu/scopus2015/1197