A Single In-Vial Dual Extraction Strategy for the Simultaneous Lipidomics and Proteomics Analysis of HDL and LDL Fractions

被引:29
作者
Godzien, Joanna [1 ]
Ciborowski, Michal [2 ]
Grace Armitage, Emily [1 ]
Jorge, Inmaculada [3 ]
Camafeita, Emilio [3 ]
Burillo, Elena [4 ]
Luis Martin-Ventura, Jose [4 ]
Ruperez, Francisco J. [1 ]
Vazquez, Jesus [3 ]
Barbas, Coral [1 ]
机构
[1] San Pablo CEU Univ, Ctr Metabol & Bioanal, CEMBIO, Madrid 28003, Spain
[2] Med Univ Bialystok, Clin Res Ctr, PL-12089 Bialystok, Poland
[3] Ctr Nacl Invest Cardiovasc Carlos III CNIC, Cardiovasc Prote Lab, Madrid 28029, Spain
[4] Univ Autonoma Madrid, Fdn Jimenez Diaz, IIS, Vasc Res Lab, Madrid 28040, Spain
关键词
lipidomics; proteomics; metabolomics; multiomics; HDL; LDL; in-vial dual extraction (IVDE); single sample extraction; lipid annotation; Apo-KO mouse; HIGH-DENSITY-LIPOPROTEIN; MASS-SPECTROMETRY; APOLIPOPROTEIN-E; HUMAN PLASMA; VITAMIN-E; METABOLIC SIGNATURE; MOUSE MODEL; PROTEINS; ATHEROSCLEROSIS; INHIBITION;
D O I
10.1021/acs.jproteome.5b00898
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A single in-vial dual extraction (IVDE) procedure for the subsequent analysis of lipids and proteins in the high density lipoprotein (HDL) and low-density lipoprotein (LDL) fractions derived from the same biological sample is presented. On the basis of methyl-tert-butyl ether (MTBE) extraction, IVDE leads to the formation of three phases: a protein pellet at the bottom, an aqueous phase with polar compounds, and an ether phase with lipophilic compounds. After sample extraction, performed within a high-performance liquid chromatography vial insert, the ether phase was directly injected for lipid fingerprinting, while the protein pellet, after evaporation of the remaining sample, was used for proteomics analysis. Human HDL and LDL isolates were used to test the suitability of the IVDE methodology for lipid and protein analysis from a single sample in terms of data quality and matching composition to that of HDL and LDL. Subsequently, HDL and LDL fractions isolated from ApoE-KO and wild-type mice were used to validate the capacity of IVDE for revealing changes in lipid and protein abundance. Results indicate that IVDE can be successfully used for the subsequent analysis of lipids and proteins with the advantages of time saving, simplicity, and reduced sample amount.
引用
收藏
页码:1762 / 1775
页数:14
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