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Related Concept Videos

Enzyme-Linked Immunosorbent Assay01:33

Enzyme-Linked Immunosorbent Assay

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In 1971, Peter Perlman and Eva Engvall developed an Enzyme-linked immunosorbent assay (ELISA or EIA). ELISA differs from western blot in that the assays are conducted in microtiter plates or in vivo rather than on an absorbent membrane.
There are many different types of ELISAs, but they all involve an antibody molecule whose constant region binds an enzyme, leaving the variable region free to bind its specific antigen.  Enzyme-substrate reaction allows the antigen to be visualized or...
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A Rapid, Multiplex Dual Reporter IgG and IgM SARS-CoV-2 Neutralization Assay for a Multiplexed Bead-Based Flow Analysis System
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SARS-CoV-2 electrochemical immunosensor based on the spike-ACE2 complex.

Viviana Vásquez1, Maria-Cristina Navas2, Javier A Jaimes3

  • 1Max Planck Tandem Group in Nanobioengieneering, Institute of Chemistry, Faculty of Natural and Exact Sciences, University of Antioquia, Complejo Ruta N, Calle 67 Nº 52-20, Medellín, 050010, Colombia.

Analytica Chimica Acta
|April 13, 2022
PubMed
Summary

A novel immunosensor rapidly detects SARS-CoV-2 spike protein for COVID-19 diagnosis. This device uses magnetic beads and antibodies, offering a sensitive and reproducible method for detecting the virus in patient samples.

Keywords:
ACE2CoronavirusImmunosensorMagnetic beadsSARS-CoV-2Spike protein

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Area of Science:

  • Biomedical Engineering
  • Immunosensors
  • Viral Diagnostics

Background:

  • Accurate and rapid diagnosis of COVID-19 is crucial for pandemic control.
  • The SARS-CoV-2 spike protein is a key target for viral detection.

Purpose of the Study:

  • To develop and validate a novel immunosensor for the rapid detection of SARS-CoV-2 spike protein.
  • To assess the sensitivity, reproducibility, and clinical applicability of the developed immunosensor.

Main Methods:

  • Fabrication of an immunosensor using magnetic beads, anti-spike and anti-ACE2 antibodies, and HRP-labeled streptavidin.
  • Detection of spike protein via sandwich assay on screen-printed gold electrodes.
  • Electrochemical signal measurement using a portable potentiostat.

Main Results:

  • The immunosensor demonstrated high sensitivity with a limit of detection of 22.5 ng/mL.
  • High reproducibility was observed in the detection of spike protein.
  • The device successfully detected SARS-CoV-2 spike protein in patient nasopharyngeal swab samples.

Conclusions:

  • The developed immunosensor provides a rapid and sensitive method for SARS-CoV-2 detection.
  • This technology has the potential for point-of-care diagnostics, bringing detection closer to the patient.
  • The immunosensor shows promise for effective COVID-19 screening and management.