PXD022689 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Calpain-mediated Protein Targets in Cardiac Mitochondria following Ischemia-Reperfusion |
Description | Calpain 1 and 2 (CPN1/2) are calcium-dependent cysteine proteases that exist in cytosol and mitochondria. Pharmacologic inhibition of CPN1/2 decreases cardiac injury during ischemia (ISC) – reperfusion (REP) by improving mitochondrial function. However, the protein targets of CPN1/2 activation during ISC-REP are unclear. CPN1/2 include a large subunit and a small regulatory subunit 1 (CPNS1). Genetic deletion of the CPNS1 eliminates the activities of both CPN1 and CPN2. Conditional, cardiomyocyte specific CPNS1 knockout (KO) mice were used in the present study to clarify the role of CPN1/2 activation in mitochondrial damage during ISC-REP with an emphasis on identifying the potential protein targets of CPN1/2. Isolated hearts from wild type (WT) or CPNS1 KO mice underwent 25 min in vitro global ISC and 30 min REP. LDH activity in coronary effluent was measured to reflect cardiac injury. Mitochondria were isolated from the hearts. Cardiac injury was decreased in CPNS1 KO mice following ISC-REP compared to WT. ISC-REP decreased the rate of oxidative phosphorylation in WT but not in CPNS1 KO mice when glutamate + malate was used as complex I substrate. KO of CPNS1 led to a smaller decrease in CRC (calcium retention capacity) following REP compared to WT. The H2O2 generation was decreased in KO mitochondria following ISC-REP compared to WT. KO of CPNS1 also resulted in less cytochrome c release from mitochondria. Proteomic analysis of the isolated mitochondria showed that KO of CPNS1 increased the abundance of ribosomal proteins and mitochondrial biogenesis proteins. These results show that activation of CPN1/2 increases cardiac injury during ischemia-reperfusion by damaging mitochondria. |
HostingRepository | PRIDE |
AnnounceDate | 2021-12-21 |
AnnouncementXML | Submission_2021-12-21_07:42:45.146.xml |
DigitalObjectIdentifier | https://dx.doi.org/10.6019/PXD022689 |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Supported dataset by repository |
PrimarySubmitter | Ling Li |
SpeciesList | scientific name: Mus musculus (Mouse); NCBI TaxID: 10090; |
ModificationList | acetylated residue; monohydroxylated residue; iodoacetamide derivatized residue |
Instrument | Orbitrap Fusion Lumos |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2020-11-24 07:50:05 | ID requested | |
⏵ 1 | 2021-12-21 07:42:45 | announced | |
Publication List
Dataset with its publication pending |
Keyword List
submitter keyword: calpain |
mitochondrial respiratory chain |
reactive oxygen species, reverse electron flow |
Contact List
Qun Chen |
contact affiliation | Departments of Medicine (Division of Cardiology), Virginia Commonwealth University, Richmond, VA, 23298 |
contact email | qun.chen@vcuhealth.org |
lab head | |
Ling Li |
contact affiliation | Cleveland Clinic |
contact email | lil5@ccf.org |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD022689
- Label: PRIDE project
- Name: Calpain-mediated Protein Targets in Cardiac Mitochondria following Ischemia-Reperfusion