# IgY antibodies/Cysteamine: simple and effective methodology for electrochemical detection of SARS-CoV-2 S-protein

**Authors:** Ariamna Gandarilla, Yonny Romaguera-Barcelay, Juliane Corrêa Glória, Luciana Freire, Taisa Farias, Jessica Feitosa, Carlos Anzola, Luís André Morais Mariuba, Walter Ricardo Brito

PMC · DOI: 10.1590/0074-02760250074 · Memórias do Instituto Oswaldo Cruz · 2025-10-20

## TL;DR

This paper presents a new electrochemical method using IgY antibodies and cysteamine to detect SARS-CoV-2 S-protein in saliva with high sensitivity and selectivity.

## Contribution

A label-free, highly sensitive electrochemical immunosensor using IgY antibodies and cysteamine for SARS-CoV-2 S-protein detection is developed.

## Key findings

- The immunosensor detected S-protein in the range of 10 to 1000 ng mL-1 with a limit of detection of 6.2 ng mL-1.
- The method outperformed ELISA in sensitivity and showed selectivity for S-protein over N-protein.
- Saliva sample tests produced results comparable to S-protein standards, indicating practical applicability.

## Abstract

The outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections was a serious disease that spread rapidly around the world and led to a state of global health emergency. During the pandemic, millions of deaths were notified as result of the progression of the disease to a serious condition. Research into the development of diagnostic tests was very important for the identification and control of new cases.

In this work a label-free electrochemical platform was developed for sensing of SARS-CoV-2 S-protein.

The S- antibodies (IgY type) from egg yolk were immobilised though stable bonding onto screen-printed gold electrodes surface, which was previously modified with self-assembled monolayers of cysteamine (Cys). The analytical performance of the devices was followed by differential pulse voltammetry after incubation in various concentrations of S-protein.

The electrical response exhibited a linear behaviour from 10 to 1000 ng mL-1 [with limit of detection (LOD) of 6.2 ng mL-1]. Also, we confirmed that our method is more sensitive than an enzyme-linked immuno-sorbent assay (ELISA), which was conducted with the same molecules (antibody and antigen) (500-4000 ng mL-1, with LOD = 235 ng mL-1). The immunosensor was selective for S-protein detection, and no significative changes were registered by differential pulse voltammetry in presence of SARS-CoV-2 N-protein. Tests on saliva samples recorded similar results to S protein standards.

The developed immunosensor showed good performance and selectivity, therefore, it can be an alternative method for coronavirus disease 2019 (Covid-19) detecting in saliva samples.

## Linked entities

- **Chemicals:** cysteamine (PubChem CID 6058)
- **Diseases:** coronavirus disease 2019 (MONDO:0100096)

## Full-text entities

- **Genes:** VTN (vitronectin) [NCBI Gene 7448] {aka V75, VN, VNT}, S (surface glycoprotein) [NCBI Gene 43740568] {aka spike glycoprotein}
- **Diseases:** infections (MESH:D007239), Covid-19 (MESH:D000086382), deaths (MESH:D003643)
- **Chemicals:** gold (MESH:D006046), Cys (MESH:D003543)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12543363/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12543363/full.md

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Source: https://tomesphere.com/paper/PMC12543363