TY - JOUR
T1 - Multi-Omic Single-Shot Technology for Integrated Proteome and Lipidome Analysis
AU - He, Yuchen
AU - Rashan, Edrees H.
AU - Linke, Vanessa
AU - Shishkova, Evgenia
AU - Hebert, Alexander S.
AU - Jochem, Adam
AU - Westphall, Michael S.
AU - Pagliarini, David J.
AU - Overmyer, Katherine A.
AU - Coon, Joshua J.
N1 - Funding Information:
We are grateful for support from NIH P41 GM108538 (J.J.C.) and NIH R35GM131795 (D.J.P.) and Robert Kennedy for helpful discussions.
Publisher Copyright:
© 2021 American Chemical Society. All rights reserved.
PY - 2021/3/9
Y1 - 2021/3/9
N2 - Mass spectrometry (MS) serves as the centerpiece technology for proteome, lipidome, and metabolome analysis. To gain a better understanding of the multifaceted networks of myriad regulatory layers in complex organisms, integration of different multiomic layers is increasingly performed, including joint extraction methods of diverse biomolecular classes and comprehensive data analyses of different omics. Despite the versatility of MS systems, fractured methodology drives nearly all MS laboratories to specialize in analysis of a single ome at the exclusion of the others. Although liquid chromatography-mass spectrometry (LC-MS) analysis is similar for different biomolecular classes, the integration on the instrument level is lagging behind. The recent advancements in high flow proteomics enable us to take a first step towards integration of protein and lipid analysis. Here, we describe a technology to achieve broad and deep coverage of multiple molecular classes simultaneously through multi-omic single-shot technology (MOST), requiring only one column, one LC-MS instrument, and a simplified workflow. MOST achieved great robustness and reproducibility. Its application to a Saccharomyces cerevisiae study consisting of 20 conditions revealed 2842 protein groups and 325 lipids and potential molecular relationships.
AB - Mass spectrometry (MS) serves as the centerpiece technology for proteome, lipidome, and metabolome analysis. To gain a better understanding of the multifaceted networks of myriad regulatory layers in complex organisms, integration of different multiomic layers is increasingly performed, including joint extraction methods of diverse biomolecular classes and comprehensive data analyses of different omics. Despite the versatility of MS systems, fractured methodology drives nearly all MS laboratories to specialize in analysis of a single ome at the exclusion of the others. Although liquid chromatography-mass spectrometry (LC-MS) analysis is similar for different biomolecular classes, the integration on the instrument level is lagging behind. The recent advancements in high flow proteomics enable us to take a first step towards integration of protein and lipid analysis. Here, we describe a technology to achieve broad and deep coverage of multiple molecular classes simultaneously through multi-omic single-shot technology (MOST), requiring only one column, one LC-MS instrument, and a simplified workflow. MOST achieved great robustness and reproducibility. Its application to a Saccharomyces cerevisiae study consisting of 20 conditions revealed 2842 protein groups and 325 lipids and potential molecular relationships.
UR - https://www.scopus.com/pages/publications/85101876228
U2 - 10.1021/acs.analchem.0c04764
DO - 10.1021/acs.analchem.0c04764
M3 - Article
C2 - 33617230
AN - SCOPUS:85101876228
SN - 0003-2700
VL - 93
SP - 4217
EP - 4222
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 9
ER -