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PXD071909
PXD071909 is an original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Characterization of extracellular vesicles from cell suspension 2 cultures of Coffea arabica L. |
| Description | A protocol was developed for the isolation and characterization of extracellular vesicles (EVs) from Coffea arabica cell suspension cultures (CSC). The isolation method involved differential ultracentrifugation of the CSC filtrate, yielding two fractions: 100,000 g for 36 minutes (100k g) and 125,000 g for 6 hours (125k g). Both fractions were characterized by size, ΞΆ potential, morphology and proteomic profiles. While no significant differences in average EV size were observed between the two fractions, proteomic analysis revealed distinct quantitative and compositional variations. The 100k g fraction was enriched in proteins associated with cell periphery, plasma membrane, and extracellular region, whereas the 125k g fraction predominantly contained proteins from the extracellular region. Proteomic marker analysis confirmed that both fractions contained protein EV markers, such as transmembrane and transport proteins, soluble EV-associated proteins and proteins targeted to extracellular environment or cell wall. Conversely, negligible contamination from non-EV-related proteins was detected. Furthermore, transmission electron microscopy (TEM) confirmed that the fractions were devoid of non-vesicular extracellular nanoparticles (NVEPs), such as exomeres and supermeres. These findings demonstrate that coffee CSC represent a valuable and scalable platform for obtaining highly pure EVs, largely free from cellular membrane contamination, thus highlighting their significant potential for biotechnological applications. |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-02-16 |
| AnnouncementXML | Submission_2026-02-15_16:22:48.355.xml |
| DigitalObjectIdentifier | https://dx.doi.org/10.6019/PXD071909 |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Supported dataset by repository |
| PrimarySubmitter | Romina Belli |
| SpeciesList | scientific name: Coffea arabica (Arabian coffee); NCBI TaxID: NEWT:13443; |
| ModificationList | acetylated residue; monohydroxylated residue; iodoacetamide derivatized residue |
| Instrument | Orbitrap Fusion |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
|---|---|---|---|
| 0 | 2025-12-12 05:54:18 | ID requested | |
| ⏵ 1 | 2026-02-15 16:22:49 | announced |
Publication List
| 10.3390/plants15030439; |
| 10.6019/PXD071909; |
| Bonaventura AD, Scarpin D, Trotta G, Marchetti S, Petrussa E, Braidot E, Navarini L, Zancani M, L. Plants (Basel), 15(3):(2026) [pubmed] |
Keyword List
| submitter keyword: cell suspension cultures |
| Coffea arabica |
| extracellular vesicles (EVs) |
| morpho-34 metric traits |
| proteomics |
| unconventional protein secretion |
Contact List
| Marco Zancani | |
|---|---|
| contact affiliation | Dept. of Agricultural, Food, Environmental and Animal Sciences (DI4A), University of Udine, 33100 Udine, Italy |
| contact email | marco.zancani@uniud.it |
| lab head | |
| Romina Belli | |
| contact affiliation | University of Trento |
| contact email | romina.belli@unitn.it |
| dataset submitter | |
Full Dataset Link List
| 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://ftp.pride.ebi.ac.uk/pride/data/archive/2026/02/PXD071909 |
| PRIDE project URI |
Repository Record List
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