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Operation Moonshot: rapid translation of a SARS-CoV-2 targeted peptide immunoaffinity liquid chromatography-tandem mass spectrometry test from research into routine clinical use

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posted on 2023-09-20, 09:37 authored by Jenny Hällqvist, Dan Lane, Andrew Shapanis, Kayleigh Davis, Wendy E Heywood, Ivan Doykov, Justyna Śpiewak, Nana Ghansah, Brian Keevil, Pankaj Gupta, Rebekah Jukes-Jones, Raj Singh, Dominic Foley, Johannes PC Vissers, Rebecca Pattison, Samantha Ferries, Robert Wardle, Amy Bartlett, Lisa J Calton, Leigh Anderson, Morteza Razavi, Terry Pearson, Matt Pope, Richard Yip, Leong L Ng, Benjamin I Nicholas, Alistair Bailey, Dan Noel, R Neil Dalton, Simon Heales, Christopher Hopley, Andrew R Pitt, Perdita Barran, Donald JL Jones, Kevin Mills, Paul Skipp, Rachel S Carling

Objectives

During 2020, the UK’s Department of Health and Social Care (DHSC) established the Moonshot programme to fund various diagnostic approaches for the detection of SARS-CoV-2, the pathogen behind the COVID-19 pandemic. Mass spectrometry was one of the technologies proposed to increase testing capacity.


Methods

Moonshot funded a multi-phase development programme, bringing together experts from academia, industry and the NHS to develop a state-of-the-art targeted protein assay utilising enrichment and liquid chromatography tandem mass spectrometry (LC-MS/MS) to capture and detect low levels of tryptic peptides derived from SARS-CoV-2 virus. The assay relies on detection of target peptides, ADETQALPQRK (ADE) and AYNVTQAFGR (AYN), derived from the nucleocapsid protein of SARS-CoV-2, measurement of which allowed the specific, sensitive, and robust detection of the virus from nasopharyngeal (NP) swabs. The diagnostic sensitivity and specificity of LC-MS/MS was compared with reverse transcription quantitative real-time polymerase chain reaction (RT-qPCR) via a prospective study.


Results

Analysis of NP swabs (n=361) with a median RT-qPCR quantification cycle (Cq) of 27 (range 16.7–39.1) demonstrated diagnostic sensitivity of 92.4% (87.4–95.5), specificity of 97.4% (94.0–98.9) and near total concordance with RT-qPCR (Cohen’s Kappa 0.90). Excluding Cq>32 samples, sensitivity was 97.9% (94.1–99.3), specificity 97.4% (94.0–98.9) and Cohen’s Kappa 0.95.


Conclusions

This unique collaboration between academia, industry and the NHS enabled development, translation, and validation of a SARS-CoV-2 method in NP swabs to be achieved in 5 months. This pilot provides a model and pipeline for future accelerated development and implementation of LC-MS/MS protein/peptide assays into the routine clinical laboratory.

History

Author affiliation

Department of Cardiovascular Sciences, University of Leicester

Version

  • VoR (Version of Record)

Published in

Clinical chemistry and laboratory medicine

Volume

61

Issue

2

Pagination

302-310

Publisher

Walter de Gruyter GmbH

issn

1434-6621

eissn

1437-4331

Copyright date

2022

Available date

2023-09-20

Spatial coverage

Germany

Language

eng

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