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pGlyco: a pipeline for the identification of intact N-glycopeptides by using HCD- and CID-MS/MS and MS3
Confident characterization of the microheterogeneity of protein glycosylation through identification of intact glycopeptides remains one of the toughest analytical challenges for glycoproteomics. Recently proposed mass spectrometry (MS)-based methods still have some defects such as lack of the false...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853738/ https://www.ncbi.nlm.nih.gov/pubmed/27139140 http://dx.doi.org/10.1038/srep25102 |
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author | Zeng, Wen-Feng Liu, Ming-Qi Zhang, Yang Wu, Jian-Qiang Fang, Pan Peng, Chao Nie, Aiying Yan, Guoquan Cao, Weiqian Liu, Chao Chi, Hao Sun, Rui-Xiang Wong, Catherine C. L. He, Si-Min Yang, Pengyuan |
author_facet | Zeng, Wen-Feng Liu, Ming-Qi Zhang, Yang Wu, Jian-Qiang Fang, Pan Peng, Chao Nie, Aiying Yan, Guoquan Cao, Weiqian Liu, Chao Chi, Hao Sun, Rui-Xiang Wong, Catherine C. L. He, Si-Min Yang, Pengyuan |
author_sort | Zeng, Wen-Feng |
collection | PubMed |
description | Confident characterization of the microheterogeneity of protein glycosylation through identification of intact glycopeptides remains one of the toughest analytical challenges for glycoproteomics. Recently proposed mass spectrometry (MS)-based methods still have some defects such as lack of the false discovery rate (FDR) analysis for the glycan identification and lack of sufficient fragmentation information for the peptide identification. Here we proposed pGlyco, a novel pipeline for the identification of intact glycopeptides by using complementary MS techniques: 1) HCD-MS/MS followed by product-dependent CID-MS/MS was used to provide complementary fragments to identify the glycans, and a novel target-decoy method was developed to estimate the false discovery rate of the glycan identification; 2) data-dependent acquisition of MS3 for some most intense peaks of HCD-MS/MS was used to provide fragments to identify the peptide backbones. By integrating HCD-MS/MS, CID-MS/MS and MS3, intact glycopeptides could be confidently identified. With pGlyco, a standard glycoprotein mixture was analyzed in the Orbitrap Fusion, and 309 non-redundant intact glycopeptides were identified with detailed spectral information of both glycans and peptides. |
format | Online Article Text |
id | pubmed-4853738 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48537382016-05-16 pGlyco: a pipeline for the identification of intact N-glycopeptides by using HCD- and CID-MS/MS and MS3 Zeng, Wen-Feng Liu, Ming-Qi Zhang, Yang Wu, Jian-Qiang Fang, Pan Peng, Chao Nie, Aiying Yan, Guoquan Cao, Weiqian Liu, Chao Chi, Hao Sun, Rui-Xiang Wong, Catherine C. L. He, Si-Min Yang, Pengyuan Sci Rep Article Confident characterization of the microheterogeneity of protein glycosylation through identification of intact glycopeptides remains one of the toughest analytical challenges for glycoproteomics. Recently proposed mass spectrometry (MS)-based methods still have some defects such as lack of the false discovery rate (FDR) analysis for the glycan identification and lack of sufficient fragmentation information for the peptide identification. Here we proposed pGlyco, a novel pipeline for the identification of intact glycopeptides by using complementary MS techniques: 1) HCD-MS/MS followed by product-dependent CID-MS/MS was used to provide complementary fragments to identify the glycans, and a novel target-decoy method was developed to estimate the false discovery rate of the glycan identification; 2) data-dependent acquisition of MS3 for some most intense peaks of HCD-MS/MS was used to provide fragments to identify the peptide backbones. By integrating HCD-MS/MS, CID-MS/MS and MS3, intact glycopeptides could be confidently identified. With pGlyco, a standard glycoprotein mixture was analyzed in the Orbitrap Fusion, and 309 non-redundant intact glycopeptides were identified with detailed spectral information of both glycans and peptides. Nature Publishing Group 2016-05-03 /pmc/articles/PMC4853738/ /pubmed/27139140 http://dx.doi.org/10.1038/srep25102 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Zeng, Wen-Feng Liu, Ming-Qi Zhang, Yang Wu, Jian-Qiang Fang, Pan Peng, Chao Nie, Aiying Yan, Guoquan Cao, Weiqian Liu, Chao Chi, Hao Sun, Rui-Xiang Wong, Catherine C. L. He, Si-Min Yang, Pengyuan pGlyco: a pipeline for the identification of intact N-glycopeptides by using HCD- and CID-MS/MS and MS3 |
title | pGlyco: a pipeline for the identification of intact N-glycopeptides by using HCD- and CID-MS/MS and MS3 |
title_full | pGlyco: a pipeline for the identification of intact N-glycopeptides by using HCD- and CID-MS/MS and MS3 |
title_fullStr | pGlyco: a pipeline for the identification of intact N-glycopeptides by using HCD- and CID-MS/MS and MS3 |
title_full_unstemmed | pGlyco: a pipeline for the identification of intact N-glycopeptides by using HCD- and CID-MS/MS and MS3 |
title_short | pGlyco: a pipeline for the identification of intact N-glycopeptides by using HCD- and CID-MS/MS and MS3 |
title_sort | pglyco: a pipeline for the identification of intact n-glycopeptides by using hcd- and cid-ms/ms and ms3 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853738/ https://www.ncbi.nlm.nih.gov/pubmed/27139140 http://dx.doi.org/10.1038/srep25102 |
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