PXD061653 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Tetraspanin-based immunocapture for high-depth proteomic profiling of extracellular vesicles from cerebrospinal fluid for biomarker discovery |
| Description | Due to its proximity to cells of the central nervous system, cerebrospinal fluid (CSF) is an important source of novel biomarkers for neurological diseases. Membrane-bound extracellular vesicles (EVs) are enriched for proteins of intracellular and membrane origin, implicated in the pathogenesis of some neurological diseases and secreted into CSF. Proteomic profiling of CSF-EVs, however, is limited by the large volumes required for typical EV isolation protocols. We appraised the performance of tetraspanin-based immunocapture to reduce required sample volume for EV isolation and subsequent proteomic profiling by library-free data independent-acquisition (DIA) mass spectrometry. Immunocapture was effective using CSF volumes as low as 200 µL, consistently detecting core EV markers and reducing relative levels of non-vesicular proteins such as Apolipoprotein B and galectin 3 binding protein (LGALS3BP) compared with size-exclusion chromatography (SEC). Proteomic depth reached 811±14 protein groups in EVs from 200 µL CSF, increasing to 1285±224 when using feature alignment across runs with up to 1000 µL starting volume. Increased depth was observed for both transmembrane and secreted proteins using immunocapture compared with SEC, with proportional enrichment of transmembrane proteins. Abundance and precursor peptide locations for potential neuronal-specific immunocapture targets described in the literature were assessed, including L1CAM and ATP1A3. This work demonstrates the effectiveness of tetraspanin immunocapture for proteomic profiling of EVs in small volumes of CSF that can be adapted to use with cell-type-specific markers of choice. |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-02-23 |
| AnnouncementXML | Submission_2026-02-22_16:24:02.980.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | iolanda Vendrell |
| SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606; |
| ModificationList | monohydroxylated residue; deamidated residue; iodoacetamide derivatized residue |
| Instrument | Orbitrap Ascend |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2025-03-10 08:36:19 | ID requested | |
| ⏵ 1 | 2026-02-22 16:24:03 | announced | |
Publication List
| Dellar ER, Vendrell I, Fischer R, Thompson AG, Tetraspanin-based immunocapture for high-depth proteomic profiling of extracellular vesicles from cerebrospinal fluid for biomarker discovery. Clin Proteomics, 23(1):8(2026) [pubmed] |
| 10.1186/s12014-025-09579-9; |
Keyword List
| submitter keyword: cerebrospinal fluid, proteomics, tetraspanin,Extracellular vesicle, immunocapture. |
Contact List
| Alexander G Thompson |
| contact affiliation | Nuffield Department of Clinical Neurosciences, University of Oxford |
| contact email | alexander.thompson@ndcn.ox.ac.uk |
| lab head | |
| iolanda Vendrell |
| contact affiliation | Target Discovery Institute, NDMRB |
| contact email | iolanda.vendrell@ndm.ox.ac.uk |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
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| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD061653
- Label: PRIDE project
- Name: Tetraspanin-based immunocapture for high-depth proteomic profiling of extracellular vesicles from cerebrospinal fluid for biomarker discovery