Data for mitochondrial proteomic alterations in the aging mouse brain

Mitochondria are dynamic organelles critical for many cellular processes, including energy generation. Thus, mitochondrial dysfunction likely plays a role in the observed alterations in brain glucose metabolism during aging. Despite implications of mitochondrial alterations during brain aging, compr...

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Main Authors: Kelly L. Stauch, Phillip R. Purnell, Lance M. Villeneuve, Howard S. Fox
Format: Article
Language:English
Published: Elsevier 2015-09-01
Series:Data in Brief
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2352340915000724
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spelling doaj-926cf41e498a4b908854024236a99d722020-11-25T01:51:11ZengElsevierData in Brief2352-34092015-09-014C12712910.1016/j.dib.2015.05.004Data for mitochondrial proteomic alterations in the aging mouse brainKelly L. StauchPhillip R. PurnellLance M. VilleneuveHoward S. FoxMitochondria are dynamic organelles critical for many cellular processes, including energy generation. Thus, mitochondrial dysfunction likely plays a role in the observed alterations in brain glucose metabolism during aging. Despite implications of mitochondrial alterations during brain aging, comprehensive quantitative proteomic studies remain limited. Therefore, to characterize the global age-associated mitochondrial proteomic changes in the brain, we analyzed mitochondria isolated from the brain of 5-, 12-, and 24-month old mice using quantitative mass spectrometry. We identified changes in the expression of proteins important for biological processes involved in the generation of precursor metabolites and energy through the breakdown of carbohydrates, lipids, and proteins. These results are significant because we identified age-associated proteomic changes suggestive of altered mitochondrial catabolic reactions during brain aging. The proteomic data described here can be found in the PRIDE Archive using the reference number PXD001370. A more comprehensive analysis of this data may be obtained from the article “Proteomic analysis and functional characterization of mouse brain mitochondria during aging reveal alterations in energy metabolism” in PROTEOMICS.http://www.sciencedirect.com/science/article/pii/S2352340915000724MitochondriaAgingProteomics
collection DOAJ
language English
format Article
sources DOAJ
author Kelly L. Stauch
Phillip R. Purnell
Lance M. Villeneuve
Howard S. Fox
spellingShingle Kelly L. Stauch
Phillip R. Purnell
Lance M. Villeneuve
Howard S. Fox
Data for mitochondrial proteomic alterations in the aging mouse brain
Data in Brief
Mitochondria
Aging
Proteomics
author_facet Kelly L. Stauch
Phillip R. Purnell
Lance M. Villeneuve
Howard S. Fox
author_sort Kelly L. Stauch
title Data for mitochondrial proteomic alterations in the aging mouse brain
title_short Data for mitochondrial proteomic alterations in the aging mouse brain
title_full Data for mitochondrial proteomic alterations in the aging mouse brain
title_fullStr Data for mitochondrial proteomic alterations in the aging mouse brain
title_full_unstemmed Data for mitochondrial proteomic alterations in the aging mouse brain
title_sort data for mitochondrial proteomic alterations in the aging mouse brain
publisher Elsevier
series Data in Brief
issn 2352-3409
publishDate 2015-09-01
description Mitochondria are dynamic organelles critical for many cellular processes, including energy generation. Thus, mitochondrial dysfunction likely plays a role in the observed alterations in brain glucose metabolism during aging. Despite implications of mitochondrial alterations during brain aging, comprehensive quantitative proteomic studies remain limited. Therefore, to characterize the global age-associated mitochondrial proteomic changes in the brain, we analyzed mitochondria isolated from the brain of 5-, 12-, and 24-month old mice using quantitative mass spectrometry. We identified changes in the expression of proteins important for biological processes involved in the generation of precursor metabolites and energy through the breakdown of carbohydrates, lipids, and proteins. These results are significant because we identified age-associated proteomic changes suggestive of altered mitochondrial catabolic reactions during brain aging. The proteomic data described here can be found in the PRIDE Archive using the reference number PXD001370. A more comprehensive analysis of this data may be obtained from the article “Proteomic analysis and functional characterization of mouse brain mitochondria during aging reveal alterations in energy metabolism” in PROTEOMICS.
topic Mitochondria
Aging
Proteomics
url http://www.sciencedirect.com/science/article/pii/S2352340915000724
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