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

Ernesto Nakayasu(Pacific Northwest National Laboratory), Carrie Nicora(Pacific Northwest National Laboratory), Amy Sims(University of North Carolina at Chapel Hill), Kristin Burnum-Johnson(Pacific Northwest National Laboratory), Young‐Mo Kim(Pacific Northwest National Laboratory), Jennifer Kyle(Pacific Northwest National Laboratory), Melissa M. Matzke(Pacific Northwest National Laboratory), Anil Shukla(Pacific Northwest National Laboratory), Rosalie Chu(Pacific Northwest National Laboratory), Athena Schepmoes(Pacific Northwest National Laboratory), Jon Jacobs(Pacific Northwest National Laboratory), Ralph S. Baric(University of North Carolina at Chapel Hill), Bobbie‐Jo Webb‐Robertson(Pacific Northwest National Laboratory), Richard Smith(Pacific Northwest National Laboratory), Thomas Metz(Pacific Northwest National Laboratory)
mSystems
May 11, 2016
Cited by 244Open Access
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Abstract

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.


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