Multiplex targeted mass spectrometry assay for one-shot flavivirus diagnosis

Targeted proteomic mass spectrometry is emerging as a salient clinical diagnostic tool to track protein biomarkers. However, its strong analytical properties have not been exploited in the diagnosis and typing of flaviviruses. Here, we report the development of a sensitive and specific single-shot r...

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Main Authors: Wee, Sheena, Alli-Shaik, Asfa, Kek, Relus, Swa, Hannah L. F., Tien, Wei-Ping, Lim, Vanessa W., Leo, Yee-Sin, Ng, Lee-Ching, Hapuarachchi, Hapuarachchige C., Gunaratne, Jayantha
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2021
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Online Access:https://hdl.handle.net/10356/151418
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1514182021-06-14T04:06:04Z Multiplex targeted mass spectrometry assay for one-shot flavivirus diagnosis Wee, Sheena Alli-Shaik, Asfa Kek, Relus Swa, Hannah L. F. Tien, Wei-Ping Lim, Vanessa W. Leo, Yee-Sin Ng, Lee-Ching Hapuarachchi, Hapuarachchige C. Gunaratne, Jayantha School of Biological Sciences Science::Biological sciences Targeted Proteomics Parallel Reaction Monitoring Targeted proteomic mass spectrometry is emerging as a salient clinical diagnostic tool to track protein biomarkers. However, its strong analytical properties have not been exploited in the diagnosis and typing of flaviviruses. Here, we report the development of a sensitive and specific single-shot robust assay for flavivirus typing and diagnosis using targeted mass spectrometry technology. Our flavivirus parallel reaction monitoring assay (fvPRM) has the ability to track secreted flaviviral nonstructural protein 1 (NS1) over a broad diagnostic and typing window with high sensitivity, specificity, extendibility, and multiplexing capability. These features, pivotal and pertinent to efficient response toward flavivirus outbreaks, including newly emerging flavivirus strains, circumvent the limitations of current diagnostic assays. fvPRM thus carries high potential in positioning itself as a forerunner in delivering early and accurate diagnosis for disease management. Agency for Science, Technology and Research (A*STAR) National Environmental Agency (NEA) We thank Siok Ghee Ler for optimizing and maintaining the LC-MS and Rachel H. X. Li for building the spectral library of DENV peptides; the Diagnostics Group at the Environmental Health Institute, Singapore, for the collection and serotyping of DENV-infected sera by PCR; and Prof. Mariano Garcia-Blanco (University of Texas Medical Branch and Duke-National University Singapore Medical School) for reading the manuscript and providing valuable feedback. The work is supported by Agency for Science, Technology and Research, Singapore and the National Environment Agency, Singapore. 2021-06-14T04:06:04Z 2021-06-14T04:06:04Z 2019 Journal Article Wee, S., Alli-Shaik, A., Kek, R., Swa, H. L. F., Tien, W., Lim, V. W., Leo, Y., Ng, L., Hapuarachchi, H. C. & Gunaratne, J. (2019). Multiplex targeted mass spectrometry assay for one-shot flavivirus diagnosis. Proceedings of the National Academy of Sciences of the United States of America, 116(14), 6754-6759. https://dx.doi.org/10.1073/pnas.1817867116 0027-8424 https://hdl.handle.net/10356/151418 10.1073/pnas.1817867116 30886083 2-s2.0-85064053237 14 116 6754 6759 en Proceedings of the National Academy of Sciences of the United States of America © 2019 The Author(s) (Published by National Academy of Sciences). All rights reserved.
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Biological sciences
Targeted Proteomics
Parallel Reaction Monitoring
spellingShingle Science::Biological sciences
Targeted Proteomics
Parallel Reaction Monitoring
Wee, Sheena
Alli-Shaik, Asfa
Kek, Relus
Swa, Hannah L. F.
Tien, Wei-Ping
Lim, Vanessa W.
Leo, Yee-Sin
Ng, Lee-Ching
Hapuarachchi, Hapuarachchige C.
Gunaratne, Jayantha
Multiplex targeted mass spectrometry assay for one-shot flavivirus diagnosis
description Targeted proteomic mass spectrometry is emerging as a salient clinical diagnostic tool to track protein biomarkers. However, its strong analytical properties have not been exploited in the diagnosis and typing of flaviviruses. Here, we report the development of a sensitive and specific single-shot robust assay for flavivirus typing and diagnosis using targeted mass spectrometry technology. Our flavivirus parallel reaction monitoring assay (fvPRM) has the ability to track secreted flaviviral nonstructural protein 1 (NS1) over a broad diagnostic and typing window with high sensitivity, specificity, extendibility, and multiplexing capability. These features, pivotal and pertinent to efficient response toward flavivirus outbreaks, including newly emerging flavivirus strains, circumvent the limitations of current diagnostic assays. fvPRM thus carries high potential in positioning itself as a forerunner in delivering early and accurate diagnosis for disease management.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Wee, Sheena
Alli-Shaik, Asfa
Kek, Relus
Swa, Hannah L. F.
Tien, Wei-Ping
Lim, Vanessa W.
Leo, Yee-Sin
Ng, Lee-Ching
Hapuarachchi, Hapuarachchige C.
Gunaratne, Jayantha
format Article
author Wee, Sheena
Alli-Shaik, Asfa
Kek, Relus
Swa, Hannah L. F.
Tien, Wei-Ping
Lim, Vanessa W.
Leo, Yee-Sin
Ng, Lee-Ching
Hapuarachchi, Hapuarachchige C.
Gunaratne, Jayantha
author_sort Wee, Sheena
title Multiplex targeted mass spectrometry assay for one-shot flavivirus diagnosis
title_short Multiplex targeted mass spectrometry assay for one-shot flavivirus diagnosis
title_full Multiplex targeted mass spectrometry assay for one-shot flavivirus diagnosis
title_fullStr Multiplex targeted mass spectrometry assay for one-shot flavivirus diagnosis
title_full_unstemmed Multiplex targeted mass spectrometry assay for one-shot flavivirus diagnosis
title_sort multiplex targeted mass spectrometry assay for one-shot flavivirus diagnosis
publishDate 2021
url https://hdl.handle.net/10356/151418
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