Electrochemical signal amplification for pathogen nucleic acid detection utilizing a cobalt-based DNA-binding metallo-intercalator

Rainbow, Joshua, Judd-Cooper, Emily P., Pope, Simon J. A., Buurma, Niklaas J. ORCID: https://orcid.org/0000-0003-0260-5057 and Estrela, Pedro 2025. Electrochemical signal amplification for pathogen nucleic acid detection utilizing a cobalt-based DNA-binding metallo-intercalator. Sensors & Diagnostics 10.1039/D4SD00322E

Preview

PDF - Published Version Available under License Creative Commons Attribution. Download (1MB) | Preview

Abstract

This paper reports the development of a highly sensitive and rapid electrochemical biosensor for the detection of pathogen nucleic acids. The primary objective was to enhance the detection sensitivity of DNA biosensors for pathogen nucleic acids commonly found in fresh and wastewaters, the food industry, and clinical samples. This enhanced sensitivity was achieved through the addition of a [Co(GA)2(aqphen)]Cl intercalating complex to increase the electrostatic field at the sensor surface/solution interface. Voltammetric and impedance-based detection techniques were employed to characterize the intercalation and redox-active properties of the compound. Additionally, non-faradaic impedance and voltammetric methods were characterized as appropriate techniques for electrochemical detection. Implementing the [Co(GA)2(aqphen)]Cl intercalator led to increased voltammetric signal output using DPV, facilitating the rapid and sensitive detection of target DNA sequences. Notably, the [Co(GA)2(aqphen)]Cl permitted detection using non-faradaic impedance in the absence of [Fe(CN)6]3−/4−. Characterization by cyclic voltammetric measurements revealed a surface-controlled redox mechanism and reversible electrochemistry of the compound intercalated with double-stranded DNA (dsDNA). Upon binding of 1 μM target DNA and 200 μM [Co(GA)2(aqphen)]Cl, a 2250% current peak increase was achieved. This increase enabled the sensitive detection of a target DNA sequence representative of E. coli DNA in buffer with an LOD of 67.5 pM, 100-fold more sensitive than the standard unlabeled assay while maintaining assay simplicity, low cost, and quick response. The use of [Co(GA)2(aqphen)]Cl among similar compounds in DNA biosensors offers a cost-effective and sensitive method for detecting waterborne pathogens such as E. coli. This approach could significantly improve environmental monitoring and pollution control by enabling more reliable and rapid monitoring of pathogens in water sources. Additionally, it has the potential to be of great use within the food industry and in point-of-care clinical settings.

Item Type:	Article
Date Type:	Published Online
Status:	In Press
Schools:	Schools > Chemistry
ISSN:	2635-0998
Funders:	EPSRC
Date of First Compliant Deposit:	16 April 2025
Date of Acceptance:	24 March 2025
Last Modified:	23 Apr 2025 11:35
URI:	https://orca.cardiff.ac.uk/id/eprint/177754

Actions (repository staff only)

Edit Item