Summary of project PR002453

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 PR002453. The data can be accessed directly via it's Project DOI: 10.21228/M8JZ5D This work is supported by NIH grant, U2C- DK119886. See: https://www.metabolomicsworkbench.org/about/howtocite.php

Project ID: PR002453
Project DOI:doi: 10.21228/M8JZ5D
Project Title:Mitochondrial control of fuel switching through de novo carnitine synthesis
Project Summary:Mitochondrial transport of trimethyllysine is the key first step in de novo biosynthesis of carnitine. In this study, we show that the uncharacterized transporter SLC25A45 mediates this step. Knockout of SLC25A45 leads to impaired fatty acid oxidation due to a decrease in carnitine. To demonstrate this, deuterated trimethyllysine (d9-TML) is traced in vitro (293 cells and primary hepatocytes) as well as subjected to mitochondrial uptake assays. MBP-SLC25A45 in E. coli is used as a non-mammalian system to study trimethyllysine uptake. We further demonstrate a decrease in acylcarnitines via our lipidomic analysis, leading to decreased cold tolerance in vivo.
Institute:BIDMC
Last Name:Auger
First Name:Christopher
Address:3 Blackfan Street, Boston, MA, 02115, USA
Email:cauger1@bidmc.harvard.edu
Phone:8579282065

Summary of all studies in project PR002453

Study IDStudy TitleSpeciesInstituteAnalysis
(* : Contains Untargted data)
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(* : Contains raw data)
ST003920 Mitochondrial control of fuel switching through de novo carnitine synthesis Mus musculus BIDMC MS 2025-12-15 1 144 Uploaded data (8.5G)*
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