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  A multiplexed microflow LC-MS/MS-PRM assay for serologic quantification of IgG N- and HPX O- glycoforms in liver fibrosis

Panigrahi, A., Zhang, L., Benicky, J., Sanda, M., Ahn, J., & Goldman, R. (2023). A multiplexed microflow LC-MS/MS-PRM assay for serologic quantification of IgG N- and HPX O- glycoforms in liver fibrosis. SCIENTIFIC REPORTS, 13(1). doi:10.1038/s41598-023-27382-0.

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Panigrahi , Aswini, Autor
Zhang, Lihua, Autor
Benicky , Julius, Autor
Sanda, Miloslav1, Autor           
Ahn, Jaeil, Autor
Goldman, Radoslav, Autor
Affiliations:
1Biomolecular Mass Spectrometry, Max Planck Institute for Heart and Lung Research, Max Planck Society, ou_2591705              

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 Zusammenfassung: Targeted quantification of glycoproteins has not reached its full potential because of limitations of the existing analytical workflows. In this study, we introduce a targeted microflow LC-MS/MS-PRM method for the quantification of multiple glycopeptides in unfractionated serum samples. The entire preparation of 16 samples in a batch is completed within 3 h, and the LC-MS quantification of all the glycoforms in a sample is completed in 15 min in triplicate, including online capture and desalting. We demonstrate applicability of the workflow on a multiplexed quantification of eight N-glycoforms of immunoglobulin G (IgG) together with two O-glycoforms of hemopexin (HPX). We applied the assay to a serologic study of fibrotic liver disease in patients of HCV etiology. The results document that specific IgG- and HPX-glycoforms detect efficiently fibrotic disease of different degree, and suggest that the LC-MS/MS-PRM assays may provide rapid and reproducible biomarker assay targeting simultaneously the N- and O-glycoforms of the peptides. We propose that such high throughput multiplexed methods may advance the clinical use of the LC-MS/MS assays.

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 Datum: 2023-01-12
 Publikationsstatus: Erschienen
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 Identifikatoren: ISI: 001006187600082
DOI: 10.1038/s41598-023-27382-0
PMID: 36635317
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Titel: SCIENTIFIC REPORTS
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 13 (1) Artikelnummer: - Start- / Endseite: - Identifikator: ISSN: 2045-2322