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

Identifieur interne : 002A37 ( PubMed/Checkpoint ); précédent : 002A36; suivant : 002A38

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

Auteurs : Ernesto S. Nakayasu [États-Unis] ; Carrie D. Nicora [États-Unis] ; Amy C. Sims [États-Unis] ; Kristin E. Burnum-Johnson [États-Unis] ; Young-Mo Kim [États-Unis] ; Jennifer E. Kyle [États-Unis] ; Melissa M. Matzke [États-Unis] ; Anil K. Shukla [États-Unis] ; Rosalie K. Chu [États-Unis] ; Athena A. Schepmoes [États-Unis] ; Jon M. Jacobs [États-Unis] ; Ralph S. Baric [États-Unis] ; Bobbie-Jo Webb-Robertson [États-Unis] ; Richard D. Smith [États-Unis] ; Thomas O. Metz [États-Unis]

Source :

RBID : pubmed:27822525

Abstract

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.

DOI: 10.1128/mSystems.00043-16
PubMed: 27822525


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pubmed:27822525

Le document en format XML

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<div type="abstract" xml:lang="en">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,
<i>in vitro</i>
, and clinical).
<b>IMPORTANCE</b>
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.
<b>Author Video</b>
: An author video summary of this article is available.</div>
</front>
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<AbstractText>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,
<i>in vitro</i>
, and clinical).
<b>IMPORTANCE</b>
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.
<b>Author Video</b>
: An author video summary of this article is available.</AbstractText>
</Abstract>
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<LastName>Nakayasu</LastName>
<ForeName>Ernesto S</ForeName>
<Initials>ES</Initials>
<AffiliationInfo>
<Affiliation>Earth & Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Nicora</LastName>
<ForeName>Carrie D</ForeName>
<Initials>CD</Initials>
<AffiliationInfo>
<Affiliation>Earth & Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Sims</LastName>
<ForeName>Amy C</ForeName>
<Initials>AC</Initials>
<AffiliationInfo>
<Affiliation>Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Burnum-Johnson</LastName>
<ForeName>Kristin E</ForeName>
<Initials>KE</Initials>
<AffiliationInfo>
<Affiliation>Earth & Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Kim</LastName>
<ForeName>Young-Mo</ForeName>
<Initials>YM</Initials>
<AffiliationInfo>
<Affiliation>Earth & Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Kyle</LastName>
<ForeName>Jennifer E</ForeName>
<Initials>JE</Initials>
<AffiliationInfo>
<Affiliation>Earth & Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Matzke</LastName>
<ForeName>Melissa M</ForeName>
<Initials>MM</Initials>
<AffiliationInfo>
<Affiliation>Earth & Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Shukla</LastName>
<ForeName>Anil K</ForeName>
<Initials>AK</Initials>
<AffiliationInfo>
<Affiliation>Earth & Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Chu</LastName>
<ForeName>Rosalie K</ForeName>
<Initials>RK</Initials>
<AffiliationInfo>
<Affiliation>Earth & Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Schepmoes</LastName>
<ForeName>Athena A</ForeName>
<Initials>AA</Initials>
<AffiliationInfo>
<Affiliation>Earth & Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Jacobs</LastName>
<ForeName>Jon M</ForeName>
<Initials>JM</Initials>
<AffiliationInfo>
<Affiliation>Earth & Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Baric</LastName>
<ForeName>Ralph S</ForeName>
<Initials>RS</Initials>
<AffiliationInfo>
<Affiliation>Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA; Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Webb-Robertson</LastName>
<ForeName>Bobbie-Jo</ForeName>
<Initials>BJ</Initials>
<AffiliationInfo>
<Affiliation>National Security Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Smith</LastName>
<ForeName>Richard D</ForeName>
<Initials>RD</Initials>
<AffiliationInfo>
<Affiliation>Earth & Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Metz</LastName>
<ForeName>Thomas O</ForeName>
<Initials>TO</Initials>
<AffiliationInfo>
<Affiliation>Earth & Biological Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington, USA.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<GrantList CompleteYN="Y">
<Grant>
<GrantID>DP3 DK094343</GrantID>
<Acronym>DK</Acronym>
<Agency>NIDDK NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>U19 AI106772</GrantID>
<Acronym>AI</Acronym>
<Agency>NIAID NIH HHS</Agency>
<Country>United States</Country>
</Grant>
</GrantList>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2016</Year>
<Month>05</Month>
<Day>10</Day>
</ArticleDate>
</Article>
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<Country>United States</Country>
<MedlineTA>mSystems</MedlineTA>
<NlmUniqueID>101680636</NlmUniqueID>
<ISSNLinking>2379-5077</ISSNLinking>
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<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">MERS-CoV</Keyword>
<Keyword MajorTopicYN="N">lipidomics</Keyword>
<Keyword MajorTopicYN="N">metabolomics</Keyword>
<Keyword MajorTopicYN="N">multi-omics analysis</Keyword>
<Keyword MajorTopicYN="N">proteomics</Keyword>
<Keyword MajorTopicYN="N">sample preparation</Keyword>
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<Month>03</Month>
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<name sortKey="Burnum Johnson, Kristin E" sort="Burnum Johnson, Kristin E" uniqKey="Burnum Johnson K" first="Kristin E" last="Burnum-Johnson">Kristin E. Burnum-Johnson</name>
<name sortKey="Chu, Rosalie K" sort="Chu, Rosalie K" uniqKey="Chu R" first="Rosalie K" last="Chu">Rosalie K. Chu</name>
<name sortKey="Jacobs, Jon M" sort="Jacobs, Jon M" uniqKey="Jacobs J" first="Jon M" last="Jacobs">Jon M. Jacobs</name>
<name sortKey="Kim, Young Mo" sort="Kim, Young Mo" uniqKey="Kim Y" first="Young-Mo" last="Kim">Young-Mo Kim</name>
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<name sortKey="Matzke, Melissa M" sort="Matzke, Melissa M" uniqKey="Matzke M" first="Melissa M" last="Matzke">Melissa M. Matzke</name>
<name sortKey="Metz, Thomas O" sort="Metz, Thomas O" uniqKey="Metz T" first="Thomas O" last="Metz">Thomas O. Metz</name>
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