Everything's under Control: Maximizing Biosensor Performance Through Negative Control Probe Selection

The rapid rise of label-free biosensing technologies has led to multiple creative strategies for the detection of macromolecules in complex biological solutions for disease state monitoring, drug discovery, and basic science research. A challenge with these techniques is that assays conducted in complex media such as serum suffer from nonspecific binding of matrix constituents. In label-free biosensors, it is virtually impossible to distinguish these nonspecific interactions without the use of a reference (negative control) probe. Only with reference subtraction can the specific binding signal be faithfully reported. To date, this has been a sparsely studied area in the biosensing field. Here, we report an FDA-inspired framework for optimum control probe selection and a systematic analysis for determining the optimal negative control probe given two monoclonal antibody capture probes on photonic ring resonator sensors. Briefly, while the differences in assay performance for IL-17A and CRP were found to be subtle, the best-scoring reference control based on the bioanalytical parameters of linearity, accuracy, and selectivity differed for each analyte. In the IL-17A assay, BSA scored the highest at 83%, while mouse IgG1 isotype control antibody placed a close second with 75%. With respect to the CRP assay, the rat IgG1 isotype control antibody scored the highest at 95%, while anti-FITC scored the second highest at 89%. These results suggest that although isotype-matching to the capture antibody may be tempting, the best on-chip reference control must be optimized on a case-by-case basis using the framework we report.