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Complexome profiling of heart mitochondria from WT and ClpP-/- mice

ABSTRACT: Mutations in the gene for the mitochondrial matrix protease CLPP can cause human Perrault syndrome, which is characterized by male and female infertility, progressive sensorineural deafness, ataxia and leukoencephalopathy. This gene encodes a peptidase that is conserved since bacteria and localizes to mitochondrial matrix in eukaryotes. To assess the assembly and stability of mitochondrial complexes heart tissue of WT and ClpP-/- mice was dissected and enriched mitochondrial fraction was used for complexome profiling.

INSTRUMENT(S): Q Exactive

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Heart

SUBMITTER: Jana Key

LAB HEAD: Georg Auburger

PROVIDER: PXD036933 | Pride | 2024-01-17

REPOSITORIES: Pride

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			Action	DRS
	Data_Analysis.xlsx	Xlsx
	Gel.tif	Other
	P21_070_Heike_MouseHeart_KO_01.raw	Raw
	P21_070_Heike_MouseHeart_KO_02.raw	Raw
	P21_070_Heike_MouseHeart_KO_03.raw	Raw

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