PXD071441 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Changes in the ATP synthase interactome in mitochondrial dysfunction by crosslinking mass spectrometry |
| Description | Mitochondrial oxidative phosphorylation (OXPHOS) comprises a series of multi-subunit protein complexes that operate in coordination with the tricarboxylic acid (TCA) cycle to generate ATP. Although these systems are metabolically interconnected, complex II is generally regarded as the only direct structural link between the OXPHOS and TCA cycle. Here, we combine in-solution crosslinking mass-spectrometry (XL-MS), quantitative proteomics, and blue native PAGE (BN-PAGE) to explore how ATP synthase (complex V) integrates within the mitochondrial metabolic network under physiological and pathological conditions. We demonstrate that in murine wild-type hearts, the F₁ catalytic head of ATP synthase forms extensive contacts with TCA cycle enzymes, establishing a previously unanticipated link between the OXPHOS and central carbon metabolism. We also found that under mitochondrial dysfunction, in this case Lrpprc-deficient hearts, where defective mitochondrial gene expression destabilizes ATP synthase, these interactions become strengthened. Moreover, ATP synthase dysfunction promotes binding of the ATPase inhibitory factor 1 (ATIF1) to the F₁ head via its N-terminal inhibitory region, shifting the ATP synthase toward an energy-preserving state. Together, our findings show that ATP synthase deficiency drives remodeling of the F₁ interactome, revealing how mitochondrial structure and regulation adapt to preserve energy homeostasis under stress. |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-05-18 |
| AnnouncementXML | Submission_2026-05-18_10:52:30.036.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Laura Pérez Pañeda |
| SpeciesList | scientific name: Mus musculus (Mouse); NCBI TaxID: NEWT:10090; |
| ModificationList | iodoacetamide derivatized residue |
| Instrument | Orbitrap Exploris 480 |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2025-12-01 14:23:33 | ID requested | |
| ⏵ 1 | 2026-05-18 10:52:30 | announced | |
Publication List
| Dataset with its publication pending |
Keyword List
| submitter keyword: ATP synthase |
| mitochondrial dysfunction |
| TCA cycle |
| crosslinking mass spectrometry |
| OXPHOS |
Contact List
| Albert J. R. Heck |
| contact affiliation | Utrecht University |
| contact email | a.j.r.heck@uu.nl |
| lab head | |
| Laura Pérez Pañeda |
| contact affiliation | Utrecht University |
| contact email | l.perezpaneda@uu.nl |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
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| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD071441
- Label: PRIDE project
- Name: Changes in the ATP synthase interactome in mitochondrial dysfunction by crosslinking mass spectrometry