Decreasing the Limits of Detection and Analysis Time of Ion Current Rectification Biosensing Measurements via a...

Improving on the analytical capabilities of a measurement is a fundamental challenge with all assays, particularly decreasing the limit of detection while maintaining a practical associated analysis time. Of late, ion current rectification (ICR) biosensing measurements have received a great deal of attention as an analyte-specific, label-free assay. In ICR biosensing, a nanopore coated with an analyte specific binding molecule (e.g., an antibody, an aptamer, etc.) is used to detect a target analyte based on the ability of the target analyte to alter the ICR response of the nanopore upon it binding to the aperture interior. This binding changes the local surface charge and/or size of the nanopore aperture, thus altering its ICR response in a time dependent manner. Here, we report the ability to enhance the transport of a target analyte molecule to and through the aperture of an antibody modified glass nanopore membrane (AMGNM) with the application of a mechanically applied pressure differential. We demonstrate that there is an optimal pressure that balances the flux of the target analyte through the AMGNM aperture with its ability to be bound and detected. Applying the optimal pressure differential allows for picomolar concentrations of the cleaved form of synaptosomal-associated protein 25 (cSNAP-25) to be detected within the same analysis time as micromolar concentrations detected without the use of the pressure differential. The methodology presented here significantly expands the utility of ICR biosensing measurements for detecting low-abundance biomolecules by lowering the limit of detection and reducing the associated analysis time.