Susanne Gimlin

This research addresses fuel biocontaminant sensing using resonant photonic gratings. The fundamental photonic resonance physics enables compact, economic sensors that provide a rapid, quantitative, and effective modality for detecting and monitoring biochemical bindings. Thus, we present resonant sensors and attendant surface chemistry targeting yeast cells as representative biofouling agents. We apply biorecognition elements (BREs) to functionalize the dielectric grating surface (TiO2) to produce a sensitive, quantitative wavelength shift-based assay for detecting Yarrowia yeast cells. Concanavalin A (Con A) is used as a BRE consisting of carbohydrate-binding proteins binding to ligands on the yeast cell surface. Corresponding resonance wavelength shifts are measured relative to concentration expressed in log10[C] where C represents the concentration of cells in solution. The assay is shown to be highly specific for detecting Yarrowia cells in various concentrations. The experimental limit of detection (LOD) of the assay is 1.92 for yeast cells in culture media and 1.22 for cells in phosphate buffer saline (PBS). The comparisons of the various functionalization methods show that (3-aminopropyl)triethoxysilane (APTES) with glutardialdehyde (GA) and Con A protocol provides optimal detection of cells in PBS.

Assessing levels of neuropeptide Y (NPY) in the human body has many medical uses. Accordingly, we report the quantitative detection of NPY biomarkers applying guided-mode resonance (GMR) biosensor methodology. The label-free sensor operates in the near-infrared spectral region exhibiting distinctive resonance signatures. The interaction of NPY with bioselective molecules on the sensor surface causes spectral shifts that directly identify the binding event without additional processing. In the experiments described here, NPY antibodies are attached to the sensor surface to impart specificity during operation. For the low concentrations of NPY of interest, we apply a sandwich NPY assay in which the sensor-linked anti-NPY molecule binds with NPY that subsequently binds with anti-NPY to close the sandwich. The sandwich assay achieves a detection limit of ~0.1 pM NPY. The photonic sensor methodology applied here enables expeditious high-throughput data acquisition with high sensitivity and specificity. The entire bioreaction is recorded as a function of time, in contrast to label-based methods with single-point detection. The convenient methodology and results reported are significant, as the NPY detection range of 0.1–10 pM demonstrated is useful in important medical circumstances.