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Coupling functionalized cobalt ferrite nanoparticle enrichment with online LC/MS/MS for top-down phosphoproteomics
Phosphorylation plays pivotal roles in cellular processes and dysregulated phosphorylation is considered as an underlying mechanism in many human diseases. Top-down mass spectrometry (MS) analyzes intact proteins and provides a comprehensive analysis of protein phosphorylation. However, top-down MS-...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5472028/ https://www.ncbi.nlm.nih.gov/pubmed/28660060 http://dx.doi.org/10.1039/c6sc05435h |
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author | Chen, Bifan Hwang, Leekyoung Ochowicz, William Lin, Ziqing Guardado-Alvarez, Tania M. Cai, Wenxuan Xiu, Lichen Dani, Kunal Colah, Cyrus Jin, Song Ge, Ying |
author_facet | Chen, Bifan Hwang, Leekyoung Ochowicz, William Lin, Ziqing Guardado-Alvarez, Tania M. Cai, Wenxuan Xiu, Lichen Dani, Kunal Colah, Cyrus Jin, Song Ge, Ying |
author_sort | Chen, Bifan |
collection | PubMed |
description | Phosphorylation plays pivotal roles in cellular processes and dysregulated phosphorylation is considered as an underlying mechanism in many human diseases. Top-down mass spectrometry (MS) analyzes intact proteins and provides a comprehensive analysis of protein phosphorylation. However, top-down MS-based phosphoproteomics is challenging due to the difficulty in enriching low abundance intact phosphoproteins as well as separating and detecting the enriched phosphoproteins from complex mixtures. Herein, we have designed and synthesized the next generation functionalized superparamagnetic cobalt ferrite (CoFe(2)O(4)) nanoparticles (NPs), and have further developed a top-down phosphoproteomics strategy coupling phosphoprotein enrichment enabled by the functionalized CoFe(2)O(4) NPs with online liquid chromatography (LC)/MS/MS for comprehensive characterization of phosphoproteins. We have demonstrated the highly specific enrichment of a minimal amount of spike-in β-casein from a complex tissue lysate as well as effective separation and quantification of its phosphorylated genetic variants. More importantly, this integrated top-down phosphoproteomics strategy allows for enrichment, identification, quantification, and comprehensive characterization of low abundance endogenous phosphoproteins from complex tissue extracts on a chromatographic time scale. |
format | Online Article Text |
id | pubmed-5472028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-54720282017-06-28 Coupling functionalized cobalt ferrite nanoparticle enrichment with online LC/MS/MS for top-down phosphoproteomics Chen, Bifan Hwang, Leekyoung Ochowicz, William Lin, Ziqing Guardado-Alvarez, Tania M. Cai, Wenxuan Xiu, Lichen Dani, Kunal Colah, Cyrus Jin, Song Ge, Ying Chem Sci Chemistry Phosphorylation plays pivotal roles in cellular processes and dysregulated phosphorylation is considered as an underlying mechanism in many human diseases. Top-down mass spectrometry (MS) analyzes intact proteins and provides a comprehensive analysis of protein phosphorylation. However, top-down MS-based phosphoproteomics is challenging due to the difficulty in enriching low abundance intact phosphoproteins as well as separating and detecting the enriched phosphoproteins from complex mixtures. Herein, we have designed and synthesized the next generation functionalized superparamagnetic cobalt ferrite (CoFe(2)O(4)) nanoparticles (NPs), and have further developed a top-down phosphoproteomics strategy coupling phosphoprotein enrichment enabled by the functionalized CoFe(2)O(4) NPs with online liquid chromatography (LC)/MS/MS for comprehensive characterization of phosphoproteins. We have demonstrated the highly specific enrichment of a minimal amount of spike-in β-casein from a complex tissue lysate as well as effective separation and quantification of its phosphorylated genetic variants. More importantly, this integrated top-down phosphoproteomics strategy allows for enrichment, identification, quantification, and comprehensive characterization of low abundance endogenous phosphoproteins from complex tissue extracts on a chromatographic time scale. Royal Society of Chemistry 2017-06-01 2017-04-07 /pmc/articles/PMC5472028/ /pubmed/28660060 http://dx.doi.org/10.1039/c6sc05435h Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Chen, Bifan Hwang, Leekyoung Ochowicz, William Lin, Ziqing Guardado-Alvarez, Tania M. Cai, Wenxuan Xiu, Lichen Dani, Kunal Colah, Cyrus Jin, Song Ge, Ying Coupling functionalized cobalt ferrite nanoparticle enrichment with online LC/MS/MS for top-down phosphoproteomics |
title | Coupling functionalized cobalt ferrite nanoparticle enrichment with online LC/MS/MS for top-down phosphoproteomics
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title_full | Coupling functionalized cobalt ferrite nanoparticle enrichment with online LC/MS/MS for top-down phosphoproteomics
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title_fullStr | Coupling functionalized cobalt ferrite nanoparticle enrichment with online LC/MS/MS for top-down phosphoproteomics
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title_full_unstemmed | Coupling functionalized cobalt ferrite nanoparticle enrichment with online LC/MS/MS for top-down phosphoproteomics
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title_short | Coupling functionalized cobalt ferrite nanoparticle enrichment with online LC/MS/MS for top-down phosphoproteomics
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title_sort | coupling functionalized cobalt ferrite nanoparticle enrichment with online lc/ms/ms for top-down phosphoproteomics |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5472028/ https://www.ncbi.nlm.nih.gov/pubmed/28660060 http://dx.doi.org/10.1039/c6sc05435h |
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