Beating the reaction limits of biosensor sensitivity with dynamic tracking of single binding events
Files
First author draft
Date
2019-03-05
Authors
Sevenler, Derin
Trueb, Jacob
Unlu, M. Selim
Version
First author draft
OA Version
Citation
Derin Sevenler, Jacob Trueb, M Selim Unlu. 2019. "Beating the reaction limits of biosensor sensitivity with dynamic tracking of single binding events." PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, Volume 116, Issue 10, pp. 4129 - 4134 (6). https://doi.org/10.1073/pnas.1815329116
Abstract
The clinical need for ultrasensitive molecular analysis has motivated the development of several endpoint-assay technologies capable of single-molecule readout. These endpoint assays are now primarily limited by the affinity and specificity of the molecular-recognition agents for the analyte of interest. In contrast, a kinetic assay with single-molecule readout could distinguish between low-abundance, high-affinity (specific analyte) and high-abundance, low-affinity (nonspecific background) binding by measuring the duration of individual binding events at equilibrium. Here, we describe such a kinetic assay, in which individual binding events are detected and monitored during sample incubation. This method uses plasmonic gold nanorods and interferometric reflectance imaging to detect thousands of individual binding events across a multiplex solid-phase sensor with a large area approaching that of leading bead-based endpoint-assay technologies. A dynamic tracking procedure is used to measure the duration of each event. From this, the total rates of binding and debinding as well as the distribution of binding-event durations are determined. We observe a limit of detection of 19 fM for a proof-of-concept synthetic DNA analyte in a 12-plex assay format.