Biolayer-Interferometry-Guided Functionalization of Screen-Printed Graphene for Label-Free Electrochemical Virus Detection

Beata M. Szydlowska, Cícero C. Pola, Zizhen Cai, Lindsay E. Chaney, Janan Hui, Robert Sheets, Jeremiah Carpenter, Delphine Dean, Jonathan C. Claussen*, Carmen L. Gomes*, Mark C. Hersam*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Additive manufacturing holds promise for rapid prototyping and low-cost production of biosensors for diverse pathogens. Among additive manufacturing methods, screen printing is particularly desirable for high-throughput production of sensing platforms. However, this technique needs to be combined with carefully formulated inks, rapid postprocessing, and selective functionalization to meet all requirements for high-performance biosensing applications. Here, we present screen-printed graphene electrodes that are processed with thermal annealing to achieve high surface area and electrical conductivity for sensitive biodetection via electrochemical impedance spectroscopy. As a proof-of-concept, this biosensing platform is utilized for electrochemical detection of SARS-CoV-2. To ensure reliable specificity in the presence of multiple variants, biolayer interferometry (BLI) is used as a label-free and dynamic screening method to identify optimal antibodies for concurrent affinity to the Spike S1 proteins of Delta, Omicron, and Wild Type SARS-CoV-2 variants while maintaining low affinity to competing pathogens such as Influenza H1N1. The BLI-identified antibodies are robustly bound to the graphene electrode surface via oxygen moieties that are introduced during the thermal annealing process. The resulting electrochemical immunosensors achieve superior metrics including rapid detection (55 s readout following 15 min of incubation), low limits of detection (approaching 500 ag/mL for the Omicron variant), and high selectivity toward multiple variants. Importantly, the sensors perform well on clinical saliva samples detecting as few as 103 copies/mL of SARS-CoV-2 Omicron, following CDC protocols. The combination of the screen-printed graphene sensing platform and effective antibody selection using BLI can be generalized to a wide range of point-of-care immunosensors.

Original languageEnglish (US)
Pages (from-to)25169-25180
Number of pages12
JournalACS Applied Materials and Interfaces
Volume16
Issue number19
DOIs
StatePublished - May 15 2024

Funding

The authors gratefully acknowledge funding support for this work from the Centers for Disease Control and Prevention under contract numbers 75D30121C10238 and U01AA029328 in addition to the National Institutes of Health under grant number U01 AA029328/AA/NIAAA NIH HHS/United States. Graphene powder production was supported by National Science Foundation Future Manufacturing Program (NSF CMMI-2037026). Screen printing was supported by the U.S. Department of Commerce, National Institute of Standards and Technology (Award 70NANB19H005) as part of the Center for Hierarchical Materials Design (CHiMaD). B.M.S. also thanks Deutsche Forschungsgemeinschaft (DFG) for funds within the framework of the Benjamin Walter Fellowship (agreement SZ 463/1-1). Figures 2 and 4 were created with BioRender.com .

Keywords

  • additive manufacturing
  • biosensing
  • electrochemical impedance spectroscopy
  • immunosensor
  • printed electronics

ASJC Scopus subject areas

  • General Materials Science

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