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PXD037974

PXD037974 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleIdentification of lysine salicylation as a novel mechanism of action of aspirin
DescriptionAspirin, one of most famous old drugs, can exert its functions through non-covalent inhibition and covalent acetylation (N-acetylation and O-acetylation) of protein targets. Here we identified lysine salicylation (Ksa) as a novel mechanism of action of aspirin in cell lines and mice. Unexpectedly, we found that aspirin treatment resulted in a reduction in glycolysis, in which the conversion of fructose-1,6-bisphosphate (FBP) to glyceraldehyde 3-phosphate (GAP) was significantly inhibited. Mechanistically, the deceased FBP turnover was unrelated or partially related to the changes in ALDOA itself or its acetylation. Instead, aspirin treatment increased cellular salicyl-CoA which salicylated ALDOA at Lys13 and Lys42, leading to reduced ALDOA activity and FBP to GAP transformation. Collectively, the discovery of a new mode of action for aspirin may expand its applications in the biomedical field.
HostingRepositoryiProX
AnnounceDate2022-11-07
AnnouncementXMLSubmission_2022-11-07_00:40:40.794.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterYanqiu Gong
SpeciesList scientific name: Homo sapiens; NCBI TaxID: 9606;
ModificationListNo PTMs are included in the dataset
InstrumentQ Exactive Plus
Dataset History
RevisionDatetimeStatusChangeLog Entry
02022-11-07 00:30:28ID requested
12022-11-07 00:40:41announced
Publication List
Dataset with its publication pending
Keyword List
submitter keyword: Aspirin, lysine salicylation, ALDOA
Contact List
Lunzhi Dai
contact affiliationSichuan University
contact emaillunzhi.dai@scu.edu.cn
lab head
Yanqiu Gong
contact affiliationSichuan University
contact emailniqiu.er@163.com
dataset submitter
Full Dataset Link List
iProX dataset URI