Proteomics

Dataset Information

0

Low abundance of the matrix arm of complex I in the mitochondria predicts longevity


ABSTRACT: The mouse liver mitochondrial proteome was analysed in four different mouse groups (allocation of the samples to Exp1 and Exp2 in brackets): AL (ad libitum fed) C57Bl6 (Exp1 129, Exp1 130, Exp2 130), DR (dietary restriction) C57Bl6 (Exp1 126, Exp1 127, Exp1 128), AL ICRFa (Exp2 128, Exp2 129) and old ICRFa (Exp2 126, Exp2 127). To achieve quantitative standardisation between Exp1 and Exp2, all 10 samples were pooled and one portion of the pool was anlaysed in each Exp (Exp1 131 and Exp2 131). Following tryptic digest and TMT 6-plex labelling, samples were separated by OffGel electrophoresis and all fractions were subsequently analysed by LCMSMS on an Orbitrap LTQ XL. One survey scan (res. 30,000) was followed by a high energy HCD scan (res. 6000) and a low energy CID scan in the LTQ. HCD data were used for the quantitation and CID data for the identification of peptides. Data were searched using Mascot (v. 2.2) through the Proteome Discoverer interface. Peptide raw quantitations were extracted as text files and further processed using dpeaqms (http://r-forge.r-project.org/projects/dpeaqms/) to obtain probability values for the differences in protein amounts for specific proteins between the different animal groups.

INSTRUMENT(S): LTQ Orbitrap

ORGANISM(S): Mus Musculus (mouse)

SUBMITTER: Achim Treumann  

PROVIDER: PXD000272 | Pride | 2014-03-18

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
091204_08_SM_TMT1_1_M.RAW Raw
091204_08_SM_TMT1_1_M.mgf Mgf
091204_09_SM_TMT1_2_M.RAW Raw
091204_09_SM_TMT1_2_M.mgf Mgf
091204_10_SM_TMT1_3_M.RAW Raw
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Publications

Low abundance of the matrix arm of complex I in mitochondria predicts longevity in mice.

Miwa Satomi S   Jow Howsun H   Baty Karen K   Johnson Amy A   Czapiewski Rafal R   Saretzki Gabriele G   Treumann Achim A   von Zglinicki Thomas T  

Nature communications 20140512


Mitochondrial function is an important determinant of the ageing process; however, the mitochondrial properties that enable longevity are not well understood. Here we show that optimal assembly of mitochondrial complex I predicts longevity in mice. Using an unbiased high-coverage high-confidence approach, we demonstrate that electron transport chain proteins, especially the matrix arm subunits of complex I, are decreased in young long-living mice, which is associated with improved complex I asse  ...[more]

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