Summary of Study ST003114

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001935. The data can be accessed directly via it's Project DOI: 10.21228/M8M430 This work is supported by NIH grant, U2C- DK119886.

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This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST003114
Study TitleLipidomics analyses in model membranes, isolated mitochondria and cellular systems to study how the local lipid environment affects BAX and BAK function during apoptosis.
Study SummaryTo investigate how the local lipid environment affects BAX and BAK function during apoptosis, we performed quantitative analyses of different lipid classes (glycerophospholipids, fatty acids, ceramides and sphingomyelins) in cultured cells, isolated mitochondria and lipid nanodics formed by Styrene-Malic Acid (SMA) co-polymers. Ceramides, sphingomyelins, fatty acids and cardiolipins were analyzed by Liquid Chromatography coupled to Tandem Mass Spectrometry (LC-MS/MS). For glycerophospholipids (PC, PE, PI, PS, PG, PA) we applied direct infusion MS approaches (Shotgun Lipidomics).
Institute
University of Cologne
DepartmentFaculty of Medicine and University Hospital of Cologne, Cluster of Excellence Cellular Stress Responses in Aging-associated Diseases (CECAD)
LaboratoryCECAD Lipidomics/Metabolomics Facility
Last NameBrodesser
First NameSusanne
AddressJoseph-Stelzmann-Str. 26, 50931 Cologne, Germany
Emailsusanne.brodesser@uk-koeln.de
Phone+49 221 478 84015
Submit Date2023-08-16
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS
Release Date2024-03-13
Release Version1
Susanne Brodesser Susanne Brodesser
https://dx.doi.org/10.21228/M8M430
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR001935
Project DOI:doi: 10.21228/M8M430
Project Title:Lipid unsaturation promotes BAX and BAK pore activity during apoptosis
Project Summary:BAX and BAK are proapoptotic members of the BCL2 family that directly mediate mitochondrial outer membrane permeabilization (MOMP), a central step in apoptosis execution. However, the molecular architecture of the mitochondrial apoptotic pore remains a key open question and especially little is known about the contribution of lipids to MOMP. By performing a comparative lipidomics analysis of the proximal membrane environment of BAK isolated in lipid nanodiscs, we find a significant enrichment of unsaturated species nearby BAK and BAX in apoptotic conditions. We then demonstrate that unsaturated lipids promote BAX pore activity in model membranes, isolated mitochondria and cellular systems, which is further supported by molecular dynamics simulations. Accordingly, the fatty acid desaturase FADS2 not only enhances apoptosis sensitivity, but also the activation of the cGAS/STING pathway downstream mtDNA release. The correlation of FADS2 levels with the sensitization to apoptosis of different lung and kidney cancer cell lines by co-treatment with unsaturated fatty acids supports the relevance of our findings. Altogether, our work provides new insight on how local lipid environment affects BAX and BAK function during apoptosis.
Institute:University of Cologne
Department:Institute for Genetics, Cluster of Excellence Cellular Stress Responses in Aging-associated Diseases (CECAD)
Last Name:García-Sáez
First Name:Ana J.
Address:Joseph-Stelzmann-Str. 26, 50931 Cologne, Germany
Email:ana.garcia@uni-koeln.de
Phone:+49 221 478 84261
Contributors:Shashank Dadsena, Rodrigo Cuevas Arenas, Gonçalo Vieira, Susanne Brodesser, Manuel N. Melo, Ana J. García-Sáez
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