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A distributable LC-MS/MS method for the measurement of serum thyroglobulin

BACKGROUND: Despite its clear advantages over immunoassay-based testing, the measurement of serum thyroglobulin by mass spectrometry remains limited to a handful of institutions. Slow adoption by clinical laboratories could reflect limited accessibility to existing methods that have sensitivity comp...

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Autores principales: Shi, Junyan, Phipps, William S., Owusu, Benjamin Y., Henderson, Clark M., Laha, Thomas J., Becker, Jessica O., Razavi, Morteza, Emrick, Michelle A., Hoofnagle, Andrew N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641599/
https://www.ncbi.nlm.nih.gov/pubmed/36388059
http://dx.doi.org/10.1016/j.jmsacl.2022.09.005
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author Shi, Junyan
Phipps, William S.
Owusu, Benjamin Y.
Henderson, Clark M.
Laha, Thomas J.
Becker, Jessica O.
Razavi, Morteza
Emrick, Michelle A.
Hoofnagle, Andrew N.
author_facet Shi, Junyan
Phipps, William S.
Owusu, Benjamin Y.
Henderson, Clark M.
Laha, Thomas J.
Becker, Jessica O.
Razavi, Morteza
Emrick, Michelle A.
Hoofnagle, Andrew N.
author_sort Shi, Junyan
collection PubMed
description BACKGROUND: Despite its clear advantages over immunoassay-based testing, the measurement of serum thyroglobulin by mass spectrometry remains limited to a handful of institutions. Slow adoption by clinical laboratories could reflect limited accessibility to existing methods that have sensitivity comparable to modern immunoassays, as well as a lack of tools for calibration and assay harmonization. METHODS: We developed and validated a liquid chromatography-tandem mass spectrometry-based assay for the quantification of serum thyroglobulin. The protocol combined peptide immunoaffinity purification using a commercially available, well-characterized monoclonal antibody and mobile phase modification with dimethylsulfoxide (DMSO) for enhanced sensitivity. To facilitate harmonization with other laboratories, we developed a novel, serum-based 5-point distributable reference material (Husky Ref). RESULTS: The assay demonstrated a lower limit of quantification of 0.15 ng/mL (<20 %CV). Mobile phase DMSO increased signal intensity of the target peptide at least 3-fold, improving quantification at low concentrations. Calibration traceable to Husky Ref enabled harmonization between laboratories in an interlaboratory study. CONCLUSIONS: Sensitive mass spectrometry-based thyroglobulin measurement can be achieved using a monoclonal antibody during peptide immunoaffinity purification and the addition of mobile phase DMSO. Laboratories interested in deploying this assay can utilize the provided standard operating procedure and freely-available Husky Ref reference material.
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spelling pubmed-96415992022-11-15 A distributable LC-MS/MS method for the measurement of serum thyroglobulin Shi, Junyan Phipps, William S. Owusu, Benjamin Y. Henderson, Clark M. Laha, Thomas J. Becker, Jessica O. Razavi, Morteza Emrick, Michelle A. Hoofnagle, Andrew N. J Mass Spectrom Adv Clin Lab Articles from the Special Issue on Quantitative Protein Mass Spectrometry to target Unmet Clinical Need BACKGROUND: Despite its clear advantages over immunoassay-based testing, the measurement of serum thyroglobulin by mass spectrometry remains limited to a handful of institutions. Slow adoption by clinical laboratories could reflect limited accessibility to existing methods that have sensitivity comparable to modern immunoassays, as well as a lack of tools for calibration and assay harmonization. METHODS: We developed and validated a liquid chromatography-tandem mass spectrometry-based assay for the quantification of serum thyroglobulin. The protocol combined peptide immunoaffinity purification using a commercially available, well-characterized monoclonal antibody and mobile phase modification with dimethylsulfoxide (DMSO) for enhanced sensitivity. To facilitate harmonization with other laboratories, we developed a novel, serum-based 5-point distributable reference material (Husky Ref). RESULTS: The assay demonstrated a lower limit of quantification of 0.15 ng/mL (<20 %CV). Mobile phase DMSO increased signal intensity of the target peptide at least 3-fold, improving quantification at low concentrations. Calibration traceable to Husky Ref enabled harmonization between laboratories in an interlaboratory study. CONCLUSIONS: Sensitive mass spectrometry-based thyroglobulin measurement can be achieved using a monoclonal antibody during peptide immunoaffinity purification and the addition of mobile phase DMSO. Laboratories interested in deploying this assay can utilize the provided standard operating procedure and freely-available Husky Ref reference material. Elsevier 2022-09-19 /pmc/articles/PMC9641599/ /pubmed/36388059 http://dx.doi.org/10.1016/j.jmsacl.2022.09.005 Text en © 2022 THE AUTHORS https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles from the Special Issue on Quantitative Protein Mass Spectrometry to target Unmet Clinical Need
Shi, Junyan
Phipps, William S.
Owusu, Benjamin Y.
Henderson, Clark M.
Laha, Thomas J.
Becker, Jessica O.
Razavi, Morteza
Emrick, Michelle A.
Hoofnagle, Andrew N.
A distributable LC-MS/MS method for the measurement of serum thyroglobulin
title A distributable LC-MS/MS method for the measurement of serum thyroglobulin
title_full A distributable LC-MS/MS method for the measurement of serum thyroglobulin
title_fullStr A distributable LC-MS/MS method for the measurement of serum thyroglobulin
title_full_unstemmed A distributable LC-MS/MS method for the measurement of serum thyroglobulin
title_short A distributable LC-MS/MS method for the measurement of serum thyroglobulin
title_sort distributable lc-ms/ms method for the measurement of serum thyroglobulin
topic Articles from the Special Issue on Quantitative Protein Mass Spectrometry to target Unmet Clinical Need
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9641599/
https://www.ncbi.nlm.nih.gov/pubmed/36388059
http://dx.doi.org/10.1016/j.jmsacl.2022.09.005
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