PXD021438
PXD021438 is an original dataset announced via ProteomeXchange.
Dataset Summary
Title | Identification of sulfenylation patterns in Plasmodium falciparum using a non-dimedone based probe |
Description | Plasmodium falciparum causes the deadliest form of malaria. Adequate redox control is crucial for this protozoan parasite to overcome oxidative and nitrosative challenges, thus enabling its survival. Sulfenylation is an oxidative post-translational modification, which acts as a molecular on/off switch, regulating protein activity. To obtain a better understanding of which proteins are redox regulated in malaria parasites, we established an optimized affinity capture protocol coupled with mass spectrometry analysis for identification of in vivo sulfenylated proteins. The non-dimedone based probe BCN-Bio1 shows reaction rates over 100-times that of commonly used dimedone-based probes, allowing for a rapid trapping of sulfenylated proteins. Mass spectrometry analysis of BCN-Bio1 labeled proteins revealed the first insight into the Plasmodium falciparum sulfenylome, identifying 102 proteins containing 152 sulfenylation sites. Comparison with Plasmodium proteins modified by S-glutathionylation and S-nitrosation showed a high overlap, suggesting a common core of proteins undergoing redox regulation by multiple mechanisms. Furthermore, parasite proteins which were identified as targets for sulfenylation were also identified as being sulfenylated in other organisms, especially proteins of the glycolytic cycle. This study suggests that a number of Plasmodium proteins are subject to redox regulation and it provides a basis for further investigations into the exact structural and biochemical basis of regulation, and a deeper understanding of cross-talk between post-translational modifications. |
HostingRepository | MassIVE |
AnnounceDate | 2021-04-09 |
AnnouncementXML | Submission_2021-04-09_11:50:57.007.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Salvador Martínez de Bartolomé |
SpeciesList | scientific name: Plasmodium falciparum; common name: malaria parasite P. falciparum; NCBI TaxID: 5833; |
ModificationList | Oxidation+NEM; unknown modification |
Instrument | LTQ Orbitrap Velos |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
---|---|---|---|
0 | 2020-09-11 16:26:04 | ID requested | |
⏵ 1 | 2021-04-09 11:50:58 | announced |
Publication List
Schipper S, Wu H, Furdui CM, Poole LB, Delahunty CM, Park R, Yates JR, Becker K, Przyborski JM, Identification of sulfenylation patterns in trophozoite stage Plasmodium falciparum using a non-dimedone based probe. Mol Biochem Parasitol, 242():111362(2021) [pubmed] |
Keyword List
submitter keyword: Sulfenylation, 9-hydroxymethylbicyclo[6.1.0]nonyne (BCN-Bio1), malaria, redox proteomics, cysteine modification, post-translational modification |
Contact List
Jude M. Przyborskia | |
---|---|
contact affiliation | Department of Biochemistry and Molecular Biology, Interdisciplinary Research Center, Justus Liebig University Giessen |
contact email | Jude.Przyborski@ernaehrung.uni-giessen.de |
lab head | |
Salvador Martínez de Bartolomé | |
contact affiliation | The Scripps Research Institute |
contact email | salvador@scripps.edu |
dataset submitter |
Full Dataset Link List
MassIVE dataset URI |
Dataset FTP location NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://massive.ucsd.edu/MSV000086125/ |