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Nanoparticle Biomolecular Corona-Based Enrichment of Plasma Glycoproteins for N-Glycan Profiling and Application in Biomarker Discovery
[Image: see text] Biomolecular corona formation has emerged as a recurring and important phenomenon in nanomedicine that has been investigated for potential applications in disease diagnosis. In this study, we have combined the “personalized protein corona” with the N-glycosylation profiling that ha...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047655/ https://www.ncbi.nlm.nih.gov/pubmed/35341249 http://dx.doi.org/10.1021/acsnano.1c09564 |
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author | Trinh, Duong N. Gardner, Richard A. Franciosi, Alessandro N. McCarthy, Cormac Keane, Michael P. Soliman, Mahmoud G. O’Donnell, James S. Meleady, Paula Spencer, Daniel I. R. Monopoli, Marco P. |
author_facet | Trinh, Duong N. Gardner, Richard A. Franciosi, Alessandro N. McCarthy, Cormac Keane, Michael P. Soliman, Mahmoud G. O’Donnell, James S. Meleady, Paula Spencer, Daniel I. R. Monopoli, Marco P. |
author_sort | Trinh, Duong N. |
collection | PubMed |
description | [Image: see text] Biomolecular corona formation has emerged as a recurring and important phenomenon in nanomedicine that has been investigated for potential applications in disease diagnosis. In this study, we have combined the “personalized protein corona” with the N-glycosylation profiling that has recently gained considerable interest in human plasma biomarker discovery as a powerful early warning diagnostic and patient stratification tool. We envisioned that the protein corona formation could be exploited as an enrichment step that is critically important in both proteomic and proteoglycomic workflows. By using silica nanoparticles, plasma fibrinogen was enriched to a level in which its proteomic and glycomic “fingerprints” could be traced with confidence. Despite being a more simplified glycan profile compared to full plasma, the corona glycan profile revealed a fibrinogen-derived glycan peak that was found to potentially distinguish lung cancer patients from controls in a pilot study. |
format | Online Article Text |
id | pubmed-9047655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90476552022-04-29 Nanoparticle Biomolecular Corona-Based Enrichment of Plasma Glycoproteins for N-Glycan Profiling and Application in Biomarker Discovery Trinh, Duong N. Gardner, Richard A. Franciosi, Alessandro N. McCarthy, Cormac Keane, Michael P. Soliman, Mahmoud G. O’Donnell, James S. Meleady, Paula Spencer, Daniel I. R. Monopoli, Marco P. ACS Nano [Image: see text] Biomolecular corona formation has emerged as a recurring and important phenomenon in nanomedicine that has been investigated for potential applications in disease diagnosis. In this study, we have combined the “personalized protein corona” with the N-glycosylation profiling that has recently gained considerable interest in human plasma biomarker discovery as a powerful early warning diagnostic and patient stratification tool. We envisioned that the protein corona formation could be exploited as an enrichment step that is critically important in both proteomic and proteoglycomic workflows. By using silica nanoparticles, plasma fibrinogen was enriched to a level in which its proteomic and glycomic “fingerprints” could be traced with confidence. Despite being a more simplified glycan profile compared to full plasma, the corona glycan profile revealed a fibrinogen-derived glycan peak that was found to potentially distinguish lung cancer patients from controls in a pilot study. American Chemical Society 2022-03-28 2022-04-26 /pmc/articles/PMC9047655/ /pubmed/35341249 http://dx.doi.org/10.1021/acsnano.1c09564 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Trinh, Duong N. Gardner, Richard A. Franciosi, Alessandro N. McCarthy, Cormac Keane, Michael P. Soliman, Mahmoud G. O’Donnell, James S. Meleady, Paula Spencer, Daniel I. R. Monopoli, Marco P. Nanoparticle Biomolecular Corona-Based Enrichment of Plasma Glycoproteins for N-Glycan Profiling and Application in Biomarker Discovery |
title | Nanoparticle
Biomolecular Corona-Based Enrichment
of Plasma Glycoproteins for N-Glycan Profiling and Application
in Biomarker Discovery |
title_full | Nanoparticle
Biomolecular Corona-Based Enrichment
of Plasma Glycoproteins for N-Glycan Profiling and Application
in Biomarker Discovery |
title_fullStr | Nanoparticle
Biomolecular Corona-Based Enrichment
of Plasma Glycoproteins for N-Glycan Profiling and Application
in Biomarker Discovery |
title_full_unstemmed | Nanoparticle
Biomolecular Corona-Based Enrichment
of Plasma Glycoproteins for N-Glycan Profiling and Application
in Biomarker Discovery |
title_short | Nanoparticle
Biomolecular Corona-Based Enrichment
of Plasma Glycoproteins for N-Glycan Profiling and Application
in Biomarker Discovery |
title_sort | nanoparticle
biomolecular corona-based enrichment
of plasma glycoproteins for n-glycan profiling and application
in biomarker discovery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9047655/ https://www.ncbi.nlm.nih.gov/pubmed/35341249 http://dx.doi.org/10.1021/acsnano.1c09564 |
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