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

**Authors:** Timothy A. Bates, Sintayehu K. Gurmessa, Jules B. Reyes-Weinstein, Eric Barklis, Fikadu G. Tafesse

PMC · DOI: 10.3390/bios16020132 · Biosensors · 2026-02-22

## TL;DR

This paper introduces a low-cost, easy-to-produce lateral flow test using nanobodies to detect SARS-CoV-2 antigens, suitable for use in areas with limited resources.

## Contribution

The study presents a novel LFA design using in-house synthesized nanobody-coated gold nanoparticles for direct antigen detection.

## Key findings

- The LFA detects SARS-CoV-2 nucleocapsid protein at 40 ng/mL with visual readout.
- The assay avoids mammalian cell culture components, reducing costs and simplifying production.
- The design is suitable for resource-limited settings due to its instrument-free operation.

## 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.

## Linked entities

- **Diseases:** SARS-CoV-2 (MONDO:0100096)

## Full-text entities

- **Genes:** N (nucleocapsid phosphoprotein) [NCBI Gene 43740575], S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}, ACSM3 (acyl-CoA synthetase medium chain family member 3) [NCBI Gene 6296] {aka SA, SAH}
- **Diseases:** infection (MESH:D007239), COVID-19 (MESH:D000086382), OPD (MESH:C538089), injury to (MESH:D014947)
- **Chemicals:** PBS (MESH:D007854), Tween-20 (MESH:D011136), IPTG (MESH:D007544), borate (MESH:D001881), citrate (MESH:D019343), Sucrose (MESH:D013395), AuNP-N42 (-), HES (MESH:D006371), HEPES (MESH:D006531), glycerol (MESH:D005990), biotin (MESH:D001710), HCl (MESH:D006851), glycine (MESH:D005998), water (MESH:D014867), imidazole (MESH:C029899), nickel (MESH:D009532), N (MESH:D009584), HAuCl4 (MESH:C024568), EDTA (MESH:D004492), His (MESH:D006639), Triton X-100 (MESH:D017830), trisodium citrate (MESH:C514290), gold (MESH:D006046), NaCl (MESH:D012965)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Trypanosoma congolense (species) [taxon 5692], Escherichia coli (E. coli, species) [taxon 562]
- **Cell lines:** BL21(DE3) E. coli — Mus musculus (Mouse), Hybridoma (CVCL_B7HM)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938044/full.md

## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938044/full.md

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Source: https://tomesphere.com/paper/PMC12938044