A colorimetric gold nanoparticle sensor to interrogate biomolecular interactions in real time on a surface.
This paper presents a new label-free optical method to study biomolecular interactions in real time at the surface of an optically transparent substrate. The method relies on the change in the absorbance spectrum of a self-assembled monolayer of colloidal gold on glass, as a function of biomolecular binding to the surface of the immobilized colloids. Using this approach, we demonstrate proof of principle of a label-free optical biosensor to quantify biomolecular interactions in real time on a surface in a commercially available UV-visible spectrophotometer and of a colorimetric end-point assay using an optical scanner. The spectrophotometric sensor shows concentration-dependent binding and a detection limit of 16 nM for streptavidin. The sensor is easy to fabricate, is reproducible in its performance, has minimal technological requirements, namely, the availability of an UV-visible spectrophotometer or an optical scanner, and will enable high-throughput screening of biomolecular interactions in real time in an array-based format.
Duke Scholars
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Related Subject Headings
- Streptavidin
- Spectrum Analysis
- Sensitivity and Specificity
- Nanotechnology
- Ligands
- Gold Colloid
- Biotin
- Biosensing Techniques
- Analytical Chemistry
- 4004 Chemical engineering
Citation
Published In
DOI
EISSN
ISSN
Publication Date
Volume
Issue
Start / End Page
Related Subject Headings
- Streptavidin
- Spectrum Analysis
- Sensitivity and Specificity
- Nanotechnology
- Ligands
- Gold Colloid
- Biotin
- Biosensing Techniques
- Analytical Chemistry
- 4004 Chemical engineering