posted on 2021-08-04, 20:13authored byApurva Bhasin, Eric J. Choi, Nicholas P. Drago, Jason E. Garrido, Emily C. Sanders, Jihoon Shin, Ilektra Andoni, Dong-Hwan Kim, Lu Fang, Gregory A. Weiss, Reginald M. Penner
The
Virus BioResistor (VBR) is a biosensor capable of rapid and
sensitive detection of small protein disease markers using a simple
dip-and-read modality. For example, the bladder cancer-associated
protein DJ-1 (22 kDa) can be detected in human urine within 1.0 min
with a limit of detection (LOD) of 10 pM. The VBR uses engineered
virus particles as receptors to recognize and selectively bind the
protein of interest. These virus particles are entrained in a conductive
poly(3,4-ethylenedioxythiophene) or PEDOT channel. The electrical
impedance of the channel increases when the target protein is bound
by the virus particles. But VBRs exhibit a sensitivity that is inversely
related to the molecular weight of the protein target. Thus, large
proteins, such as IgG antibodies (150 kDa), can be undetectable even
at high concentrations. We demonstrate that the electrochemical overoxidation
of the VBR’s PEDOT channel increases its electrical impedance,
conferring enhanced sensitivity for both small and large proteins.
Overoxidation makes possible the detection of two antibodies, undetectable
at a normal VBR, with a limit of detection of 40 ng/mL (250 pM), and
a dynamic range for quantitation extending to 600 ng/mL.