Proteomics

Dataset Information

The assembly of the Mitochondrial Complex I Assembly complex uncovers a redox pathway coordination


ABSTRACT: The Mitochondrial Complex I Assembly (MCIA) complex is essential for the biogenesis of respiratory Complex I (CI), the first enzyme in the respiratory chain, which has been linked to Alzheimer’s disease (AD) pathogenesis. However, how MCIA facilitates CI assembly, and how it is linked with AD pathogenesis, is poorly understood. Here we report the structural basis of the complex formation between the MCIA subunits ECSIT and ACAD9. ECSIT binding induces a major conformational change in the FAD-binding loop of ACAD9, releasing the FAD cofactor and converting ACAD9 from a fatty acid β-oxidation (FAO) enzyme to a CI assembly factor. We provide evidence that ECSIT phosphorylation downregulates its association with ACAD9 and is reduced in neuronal cells upon exposure to amyloid-β (Aβ) oligomers. These findings advance our understanding of the MCIA complex assembly and suggest a possible role for ECSIT in the reprogramming of bioenergetic pathways linked to Aβ toxicity, a hallmark of AD.

INSTRUMENT(S):

ORGANISM(S): Homo Sapiens (human) Escherichia Coli

SUBMITTER: Jennifer Schwarz  

LAB HEAD: Montserrat Soler-Lopez

PROVIDER: PXD042905 | Pride | 2023-12-13

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
PXD042905_community_annotated.sdrf.tsv Tabular
UP000005640_9606_ECSITHisCterm.fasta Fasta
Zelda_220311_P2012_JS_SA_B1_T_R1.raw Raw
Zelda_220311_P2012_JS_SA_B2_T_R1.raw Raw
Zelda_220311_P2012_JS_SA_B3_T_R1.raw Raw
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