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February 24, 20264 citationsOpen Access

A Nanobody-Based Lateral Flow Assay for Point-of-Care Diagnostics

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TBTimothy C. BatesSGSintayehu K GurmessaJRJules B. Reyes-Weinstein

Key Points

  • This research aims to develop a cost-effective and easily manufacturable LFA for detecting SARS-CoV-2.
  • Developed a nanobody-based lateral flow assay for SARS-CoV-2 nucleocapsid protein.
  • Synthetized Nb-coated gold nanoparticles for visual detection.
  • Tested the assay for direct antigen detection without requiring complex equipment.
  • The device can detect SARS-CoV-2 nucleocapsid protein down to 40 ng/mL.
  • Eliminates the need for mammalian cell culture components.
  • Designed for easy production with in-house reagents, reducing costs.

Abstract

Lateral flow assays (LFAs) are among the most successful technologies for point-of-care and at-home testing, but further advances are needed to reduce costs and accelerate development. Alpaca-derived nanobodies (Nbs), single-domain antibody fragments, are promising immunoassay reagents across diverse applications. Their small size and ease of recombinant production make them particularly well suited for diagnostics. Here, we present a paper-based LFA targeting the SARS-CoV-2 nucleocapsid (N) protein that exclusively uses Nbs for direct antigen detection. We also demonstrate in-house synthesis of Nb-coated gold nanoparticles, enabling instrument-free visual readout and detection of N protein down to 40 ng/mL. This design avoids components that require mammalian cell culture and can be produced entirely from in-house reagents, simplifying manufacturing and lowering component costs. Because the assay is read visually without an external reader, it is well suited for deployment in resource-limited settings. Together, these results highlight the speed and practicality of developing Nb-based LFAs and suggest a broadly applicable strategy for detecting other clinically important disease biomarkers.

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Cite This Study

Bates et al. (2026) studied this question.

synapsesocial.com/papers/699d3fb3de8e28729cf64703https://doi.org/10.3390/bios16020132
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