A rapid, ultrasensitive voltammetric biosensor for determining SARS-CoV-2 spike protein in real samples.

Biosens Bioelectron

Department of Medical Microbiology and Medical Biotechnology, Acibadem University, 34752, Istanbul, Turkey.

Published: November 2021

AI Article Synopsis

  • The COVID-19 pandemic has created a global public health threat, emphasizing the need for early diagnosis.
  • This article introduces a new sensor that uses voltammetry to detect SARS-CoV-2 spike protein, combining bovine serum albumin, antibodies, and functionalized graphene oxide on electrodes.
  • The sensors can identify extremely low levels of the virus in various samples quickly and show high specificity and sensitivity compared to traditional methods like RT-PCR and rapid antigen tests, suggesting they could be valuable tools for COVID-19 diagnosis.

Article Abstract

The ongoing coronavirus disease 2019 (COVID-19) pandemic continues to threaten public health systems all around the world. In controlling the viral outbreak, early diagnosis of COVID-19 is pivotal. This article describes a novel method of voltammetrically determining severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein with a newly designed sensor involving bovine serum albumin, SARS-CoV-2 spike antibody and a functionalised graphene oxide modified glassy carbon electrode (BSA/AB/f-GO/GCE) or screen-printed electrode (BSA/AB/f-GO/SPE). The oxidation reaction based on the antibody-antigen protein interaction was evaluated as a response to SARS-CoV-2 spike protein at -200 mV and 1430 mV with the BSA/AB/f-GO/SPE and BSA/AB/f-GO/GCE, respectively. The developed sensors, BSA/AB/f-GO/SPE and BSA/AB/f-GO/GCE, could detect 1 ag/mL of virus spike protein in synthetic, saliva and oropharyngeal swab samples in 5 min and 35 min, and both sensors demonstrated a dynamic response to the SARS-CoV-2 spike protein between 1 ag/mL and 10 fg/mL. Real-time polymerase chain reaction (RT-PCR), rapid antigen test and the proposed method were applied to saliva samples. When compared to RT-PCR, it was observed that the developed method had a 92.5% specificity and 93.3% sensitivity. Moreover, BSA/AB/f-GO/SPE sensor achieved 91.7% accuracy compared to 66.7% accuracy of rapid antigen test kit in positive samples. In view of these findings, the developed sensor provides great potential for the diagnosing of COVID-19 in real samples.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8276568PMC
http://dx.doi.org/10.1016/j.bios.2021.113497DOI Listing

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