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MPLEx: a Robust and Universal Protocol for Single-Sample Integrative Proteomic, Metabolomic, and Lipidomic Analyses

Integrative multi-omics analyses can empower more effective investigation and complete understanding of complex biological systems. Despite recent advances in a range of omics analyses, multi-omic measurements of the same sample are still challenging and current methods have not been well evaluated...

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Autores principales: Nakayasu, Ernesto S., Nicora, Carrie D., Sims, Amy C., Burnum-Johnson, Kristin E., Kim, Young-Mo, Kyle, Jennifer E., Matzke, Melissa M., Shukla, Anil K., Chu, Rosalie K., Schepmoes, Athena A., Jacobs, Jon M., Baric, Ralph S., Webb-Robertson, Bobbie-Jo, Smith, Richard D., Metz, Thomas O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069757/
https://www.ncbi.nlm.nih.gov/pubmed/27822525
http://dx.doi.org/10.1128/mSystems.00043-16
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author Nakayasu, Ernesto S.
Nicora, Carrie D.
Sims, Amy C.
Burnum-Johnson, Kristin E.
Kim, Young-Mo
Kyle, Jennifer E.
Matzke, Melissa M.
Shukla, Anil K.
Chu, Rosalie K.
Schepmoes, Athena A.
Jacobs, Jon M.
Baric, Ralph S.
Webb-Robertson, Bobbie-Jo
Smith, Richard D.
Metz, Thomas O.
author_facet Nakayasu, Ernesto S.
Nicora, Carrie D.
Sims, Amy C.
Burnum-Johnson, Kristin E.
Kim, Young-Mo
Kyle, Jennifer E.
Matzke, Melissa M.
Shukla, Anil K.
Chu, Rosalie K.
Schepmoes, Athena A.
Jacobs, Jon M.
Baric, Ralph S.
Webb-Robertson, Bobbie-Jo
Smith, Richard D.
Metz, Thomas O.
author_sort Nakayasu, Ernesto S.
collection PubMed
description Integrative multi-omics analyses can empower more effective investigation and complete understanding of complex biological systems. Despite recent advances in a range of omics analyses, multi-omic measurements of the same sample are still challenging and current methods have not been well evaluated in terms of reproducibility and broad applicability. Here we adapted a solvent-based method, widely applied for extracting lipids and metabolites, to add proteomics to mass spectrometry-based multi-omics measurements. The metabolite, protein, and lipid extraction (MPLEx) protocol proved to be robust and applicable to a diverse set of sample types, including cell cultures, microbial communities, and tissues. To illustrate the utility of this protocol, an integrative multi-omics analysis was performed using a lung epithelial cell line infected with Middle East respiratory syndrome coronavirus, which showed the impact of this virus on the host glycolytic pathway and also suggested a role for lipids during infection. The MPLEx method is a simple, fast, and robust protocol that can be applied for integrative multi-omic measurements from diverse sample types (e.g., environmental, in vitro, and clinical). IMPORTANCE In systems biology studies, the integration of multiple omics measurements (i.e., genomics, transcriptomics, proteomics, metabolomics, and lipidomics) has been shown to provide a more complete and informative view of biological pathways. Thus, the prospect of extracting different types of molecules (e.g., DNAs, RNAs, proteins, and metabolites) and performing multiple omics measurements on single samples is very attractive, but such studies are challenging due to the fact that the extraction conditions differ according to the molecule type. Here, we adapted an organic solvent-based extraction method that demonstrated broad applicability and robustness, which enabled comprehensive proteomics, metabolomics, and lipidomics analyses from the same sample. Author Video: An author video summary of this article is available.
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spelling pubmed-50697572016-11-07 MPLEx: a Robust and Universal Protocol for Single-Sample Integrative Proteomic, Metabolomic, and Lipidomic Analyses Nakayasu, Ernesto S. Nicora, Carrie D. Sims, Amy C. Burnum-Johnson, Kristin E. Kim, Young-Mo Kyle, Jennifer E. Matzke, Melissa M. Shukla, Anil K. Chu, Rosalie K. Schepmoes, Athena A. Jacobs, Jon M. Baric, Ralph S. Webb-Robertson, Bobbie-Jo Smith, Richard D. Metz, Thomas O. mSystems Research Article Integrative multi-omics analyses can empower more effective investigation and complete understanding of complex biological systems. Despite recent advances in a range of omics analyses, multi-omic measurements of the same sample are still challenging and current methods have not been well evaluated in terms of reproducibility and broad applicability. Here we adapted a solvent-based method, widely applied for extracting lipids and metabolites, to add proteomics to mass spectrometry-based multi-omics measurements. The metabolite, protein, and lipid extraction (MPLEx) protocol proved to be robust and applicable to a diverse set of sample types, including cell cultures, microbial communities, and tissues. To illustrate the utility of this protocol, an integrative multi-omics analysis was performed using a lung epithelial cell line infected with Middle East respiratory syndrome coronavirus, which showed the impact of this virus on the host glycolytic pathway and also suggested a role for lipids during infection. The MPLEx method is a simple, fast, and robust protocol that can be applied for integrative multi-omic measurements from diverse sample types (e.g., environmental, in vitro, and clinical). IMPORTANCE In systems biology studies, the integration of multiple omics measurements (i.e., genomics, transcriptomics, proteomics, metabolomics, and lipidomics) has been shown to provide a more complete and informative view of biological pathways. Thus, the prospect of extracting different types of molecules (e.g., DNAs, RNAs, proteins, and metabolites) and performing multiple omics measurements on single samples is very attractive, but such studies are challenging due to the fact that the extraction conditions differ according to the molecule type. Here, we adapted an organic solvent-based extraction method that demonstrated broad applicability and robustness, which enabled comprehensive proteomics, metabolomics, and lipidomics analyses from the same sample. Author Video: An author video summary of this article is available. American Society for Microbiology 2016-05-10 /pmc/articles/PMC5069757/ /pubmed/27822525 http://dx.doi.org/10.1128/mSystems.00043-16 Text en Copyright © 2016 Nakayasu et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Nakayasu, Ernesto S.
Nicora, Carrie D.
Sims, Amy C.
Burnum-Johnson, Kristin E.
Kim, Young-Mo
Kyle, Jennifer E.
Matzke, Melissa M.
Shukla, Anil K.
Chu, Rosalie K.
Schepmoes, Athena A.
Jacobs, Jon M.
Baric, Ralph S.
Webb-Robertson, Bobbie-Jo
Smith, Richard D.
Metz, Thomas O.
MPLEx: a Robust and Universal Protocol for Single-Sample Integrative Proteomic, Metabolomic, and Lipidomic Analyses
title MPLEx: a Robust and Universal Protocol for Single-Sample Integrative Proteomic, Metabolomic, and Lipidomic Analyses
title_full MPLEx: a Robust and Universal Protocol for Single-Sample Integrative Proteomic, Metabolomic, and Lipidomic Analyses
title_fullStr MPLEx: a Robust and Universal Protocol for Single-Sample Integrative Proteomic, Metabolomic, and Lipidomic Analyses
title_full_unstemmed MPLEx: a Robust and Universal Protocol for Single-Sample Integrative Proteomic, Metabolomic, and Lipidomic Analyses
title_short MPLEx: a Robust and Universal Protocol for Single-Sample Integrative Proteomic, Metabolomic, and Lipidomic Analyses
title_sort mplex: a robust and universal protocol for single-sample integrative proteomic, metabolomic, and lipidomic analyses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069757/
https://www.ncbi.nlm.nih.gov/pubmed/27822525
http://dx.doi.org/10.1128/mSystems.00043-16
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