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Ratiometric Mass Spectrometry for Cell Identification and Quantitation Using Intracellular “Dual-Biomarkers”

This study proposed an easy-to-use method for cell identification and quantitation by ratiometric matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). Two pairs of MS peaks in the molecular fingerprint of cells were selected as intracellular dual-biomarkers du...

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Autores principales: Chen, Xiaoming, Wo, Fangjie, Chen, Jiang, Tan, Jie, Wang, Tao, Liang, Xiao, Wu, Jianmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727126/
https://www.ncbi.nlm.nih.gov/pubmed/29234137
http://dx.doi.org/10.1038/s41598-017-17812-1
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author Chen, Xiaoming
Wo, Fangjie
Chen, Jiang
Tan, Jie
Wang, Tao
Liang, Xiao
Wu, Jianmin
author_facet Chen, Xiaoming
Wo, Fangjie
Chen, Jiang
Tan, Jie
Wang, Tao
Liang, Xiao
Wu, Jianmin
author_sort Chen, Xiaoming
collection PubMed
description This study proposed an easy-to-use method for cell identification and quantitation by ratiometric matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). Two pairs of MS peaks in the molecular fingerprint of cells were selected as intracellular dual-biomarkers due to the stability and specificity of their ratio values in different types of hepatocellular cancer (HCC) cell lines. Five types of HCC cells can be thereafter differentiated based on these two pairs of intracellular peptides/proteins. Two types of HCC cells, Huh7 and LM3 were co-cultured as a model to test whether the method is feasible for cell quantitation. The results indicated that the ratiometric peak intensity of the two pair biomarkers exhibits linear relationship with the proportion of Huh7 cells. Furthermore, tumor heterogeneity was simulated by subcutaneously injecting the co-cultured cells into nude mice. The cell type and proportion in the section of grown tumor tissue can be discriminated using the ratiometric MALDI imaging approach. LC-MS/MS detection revealed that one of the biomarker pairs belongs to thymosin family, β4 and β10. The ratiometric MS spectral approach using intracellular dual-biomarkers might become a pervasive strategy for high-throughput cell identification and quantitation, which is vital in tumor heterogeneity study, clinical diagnosis and drug screening.
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spelling pubmed-57271262017-12-13 Ratiometric Mass Spectrometry for Cell Identification and Quantitation Using Intracellular “Dual-Biomarkers” Chen, Xiaoming Wo, Fangjie Chen, Jiang Tan, Jie Wang, Tao Liang, Xiao Wu, Jianmin Sci Rep Article This study proposed an easy-to-use method for cell identification and quantitation by ratiometric matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). Two pairs of MS peaks in the molecular fingerprint of cells were selected as intracellular dual-biomarkers due to the stability and specificity of their ratio values in different types of hepatocellular cancer (HCC) cell lines. Five types of HCC cells can be thereafter differentiated based on these two pairs of intracellular peptides/proteins. Two types of HCC cells, Huh7 and LM3 were co-cultured as a model to test whether the method is feasible for cell quantitation. The results indicated that the ratiometric peak intensity of the two pair biomarkers exhibits linear relationship with the proportion of Huh7 cells. Furthermore, tumor heterogeneity was simulated by subcutaneously injecting the co-cultured cells into nude mice. The cell type and proportion in the section of grown tumor tissue can be discriminated using the ratiometric MALDI imaging approach. LC-MS/MS detection revealed that one of the biomarker pairs belongs to thymosin family, β4 and β10. The ratiometric MS spectral approach using intracellular dual-biomarkers might become a pervasive strategy for high-throughput cell identification and quantitation, which is vital in tumor heterogeneity study, clinical diagnosis and drug screening. Nature Publishing Group UK 2017-12-12 /pmc/articles/PMC5727126/ /pubmed/29234137 http://dx.doi.org/10.1038/s41598-017-17812-1 Text en © The Author(s) 2017 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
Chen, Xiaoming
Wo, Fangjie
Chen, Jiang
Tan, Jie
Wang, Tao
Liang, Xiao
Wu, Jianmin
Ratiometric Mass Spectrometry for Cell Identification and Quantitation Using Intracellular “Dual-Biomarkers”
title Ratiometric Mass Spectrometry for Cell Identification and Quantitation Using Intracellular “Dual-Biomarkers”
title_full Ratiometric Mass Spectrometry for Cell Identification and Quantitation Using Intracellular “Dual-Biomarkers”
title_fullStr Ratiometric Mass Spectrometry for Cell Identification and Quantitation Using Intracellular “Dual-Biomarkers”
title_full_unstemmed Ratiometric Mass Spectrometry for Cell Identification and Quantitation Using Intracellular “Dual-Biomarkers”
title_short Ratiometric Mass Spectrometry for Cell Identification and Quantitation Using Intracellular “Dual-Biomarkers”
title_sort ratiometric mass spectrometry for cell identification and quantitation using intracellular “dual-biomarkers”
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727126/
https://www.ncbi.nlm.nih.gov/pubmed/29234137
http://dx.doi.org/10.1038/s41598-017-17812-1
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