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Facile carrier-assisted targeted mass spectrometric approach for proteomic analysis of low numbers of mammalian cells

There is an unmet technical challenge for mass spectrometry (MS)-based proteomic analysis of single mammalian cells. Quantitative proteomic analysis of single cells has been previously achieved by antibody-based immunoassays but is limited by the availability of high-quality antibodies. Herein we re...

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Autores principales: Shi, Tujin, Gaffrey, Matthew J., Fillmore, Thomas L., Nicora, Carrie D., Yi, Lian, Zhang, Pengfei, Shukla, Anil K., Wiley, H. Steven, Rodland, Karin D., Liu, Tao, Smith, Richard D., Qian, Wei-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123794/
https://www.ncbi.nlm.nih.gov/pubmed/30271983
http://dx.doi.org/10.1038/s42003-018-0107-6
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author Shi, Tujin
Gaffrey, Matthew J.
Fillmore, Thomas L.
Nicora, Carrie D.
Yi, Lian
Zhang, Pengfei
Shukla, Anil K.
Wiley, H. Steven
Rodland, Karin D.
Liu, Tao
Smith, Richard D.
Qian, Wei-Jun
author_facet Shi, Tujin
Gaffrey, Matthew J.
Fillmore, Thomas L.
Nicora, Carrie D.
Yi, Lian
Zhang, Pengfei
Shukla, Anil K.
Wiley, H. Steven
Rodland, Karin D.
Liu, Tao
Smith, Richard D.
Qian, Wei-Jun
author_sort Shi, Tujin
collection PubMed
description There is an unmet technical challenge for mass spectrometry (MS)-based proteomic analysis of single mammalian cells. Quantitative proteomic analysis of single cells has been previously achieved by antibody-based immunoassays but is limited by the availability of high-quality antibodies. Herein we report a facile targeted MS-based proteomics method, termed cPRISM-SRM (carrier-assisted high-pressure, high-resolution separations with intelligent selection and multiplexing coupled to selected reaction monitoring), for reliable analysis of low numbers of mammalian cells. The method capitalizes on using “carrier protein” to assist processing of low numbers of cells with minimal loss, high-resolution PRISM separation for target peptide enrichment, and sensitive SRM for protein quantification. We have demonstrated that cPRISM-SRM has sufficient sensitivity to quantify proteins expressed at ≥200,000 copies per cell at the single-cell level and ≥3000 copies per cell in 100 mammalian cells. We envision that with further improvement cPRISM-SRM has the potential to move toward targeted MS-based single-cell proteomics.
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spelling pubmed-61237942018-09-28 Facile carrier-assisted targeted mass spectrometric approach for proteomic analysis of low numbers of mammalian cells Shi, Tujin Gaffrey, Matthew J. Fillmore, Thomas L. Nicora, Carrie D. Yi, Lian Zhang, Pengfei Shukla, Anil K. Wiley, H. Steven Rodland, Karin D. Liu, Tao Smith, Richard D. Qian, Wei-Jun Commun Biol Article There is an unmet technical challenge for mass spectrometry (MS)-based proteomic analysis of single mammalian cells. Quantitative proteomic analysis of single cells has been previously achieved by antibody-based immunoassays but is limited by the availability of high-quality antibodies. Herein we report a facile targeted MS-based proteomics method, termed cPRISM-SRM (carrier-assisted high-pressure, high-resolution separations with intelligent selection and multiplexing coupled to selected reaction monitoring), for reliable analysis of low numbers of mammalian cells. The method capitalizes on using “carrier protein” to assist processing of low numbers of cells with minimal loss, high-resolution PRISM separation for target peptide enrichment, and sensitive SRM for protein quantification. We have demonstrated that cPRISM-SRM has sufficient sensitivity to quantify proteins expressed at ≥200,000 copies per cell at the single-cell level and ≥3000 copies per cell in 100 mammalian cells. We envision that with further improvement cPRISM-SRM has the potential to move toward targeted MS-based single-cell proteomics. Nature Publishing Group UK 2018-08-06 /pmc/articles/PMC6123794/ /pubmed/30271983 http://dx.doi.org/10.1038/s42003-018-0107-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shi, Tujin
Gaffrey, Matthew J.
Fillmore, Thomas L.
Nicora, Carrie D.
Yi, Lian
Zhang, Pengfei
Shukla, Anil K.
Wiley, H. Steven
Rodland, Karin D.
Liu, Tao
Smith, Richard D.
Qian, Wei-Jun
Facile carrier-assisted targeted mass spectrometric approach for proteomic analysis of low numbers of mammalian cells
title Facile carrier-assisted targeted mass spectrometric approach for proteomic analysis of low numbers of mammalian cells
title_full Facile carrier-assisted targeted mass spectrometric approach for proteomic analysis of low numbers of mammalian cells
title_fullStr Facile carrier-assisted targeted mass spectrometric approach for proteomic analysis of low numbers of mammalian cells
title_full_unstemmed Facile carrier-assisted targeted mass spectrometric approach for proteomic analysis of low numbers of mammalian cells
title_short Facile carrier-assisted targeted mass spectrometric approach for proteomic analysis of low numbers of mammalian cells
title_sort facile carrier-assisted targeted mass spectrometric approach for proteomic analysis of low numbers of mammalian cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123794/
https://www.ncbi.nlm.nih.gov/pubmed/30271983
http://dx.doi.org/10.1038/s42003-018-0107-6
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