1. Academic Validation
  2. Recreating the biological steps of viral infection on a cell-free bioelectronic platform to profile viral variants of concern

Recreating the biological steps of viral infection on a cell-free bioelectronic platform to profile viral variants of concern

  • Nat Commun. 2024 Jul 3;15(1):5606. doi: 10.1038/s41467-024-49415-6.
Zhongmou Chao # 1 Ekaterina Selivanovitch # 1 Konstantinos Kallitsis 2 Zixuan Lu 2 Ambika Pachaury 1 Róisín Owens 2 Susan Daniel 3
Affiliations

Affiliations

  • 1 Robert Frederick Smith School of Chemical and Biomolecular Engineering, Cornell University, 124 Olin Hall, Ithaca, NY, 14853, USA.
  • 2 Department of Chemical Engineering and Biotechnology, University of Cambridge, Philippa Fawcett Dr., Cambridge, CB3 0AS, UK.
  • 3 Robert Frederick Smith School of Chemical and Biomolecular Engineering, Cornell University, 124 Olin Hall, Ithaca, NY, 14853, USA. sd386@cornell.edu.
  • # Contributed equally.
Abstract

Viral mutations frequently outpace technologies used to detect harmful variants. Given the continual emergence of SARS-CoV-2 variants, platforms that can identify the presence of a virus and its propensity for Infection are needed. Our electronic biomembrane sensing platform recreates distinct SARS-CoV-2 host cell entry pathways and reports the progression of entry as electrical signals. We focus on two necessary entry processes mediated by the viral Spike protein: virus binding and membrane fusion, which can be distinguished electrically. We find that closely related variants of concern exhibit distinct fusion signatures that correlate with trends in cell-based infectivity assays, allowing us to report quantitative differences in their fusion characteristics and hence their infectivity potentials. We use SARS-CoV-2 as our prototype, but we anticipate that this platform can extend to other enveloped viruses and cell lines to quantifiably assess virus entry.

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