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PXD061101
PXD061101 is an original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Identification of MHC ligands through allele guided isolation combined with machine learning for specific MHC assignment |
| Description | Isolation of MHC ligands and subsequent analysis by mass spectrometry is considered the gold standard for defining targets for T cell-based immunotherapies. However, as many targets of high tumor-specificity are only presented at low abundance on the cell surface of tumor cells, the efficient isolation of these peptides is crucial for their successful detection. Furthermore, since multiple MHC alleles can present the same MHC ligand, improving the prediction and assignment to a specific MHC allele is highly desirable. Here, we demonstrate how optimizations of the MHC ligand isolation strategy support the identification of specific MHC ligands and how the hydrophobicity of presented peptides as well as their post-translational modifications need to be considered as exemplified by, the detection of cysteinylated MHC ligands from cancer germline antigens or point-mutated neoepitopes. To further improve the identification and characterization of MHC ligands, we developed a novel MHC class I ligand prediction algorithm (ARDisplay-I) that outperforms the current state-of-the-art. Moreover, ARDisplay-I facilitates the assignment of peptides to the appropriate MHC allele, especially if multiple alleles have to be considered. Implementing these strategies can augment the development of T cell receptor-based therapies by facilitating the identification of novel immunotherapy targets and enriching the resources available in the computational immunology field. |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-06-08 |
| AnnouncementXML | Submission_2026-06-07_17:10:40.485.xml |
| DigitalObjectIdentifier | https://doi.org/10.6019/PXD061101 |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Supported dataset by repository |
| PrimarySubmitter | Martin Klatt |
| SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: NEWT:9606; |
| ModificationList | cysteinylation (disulfide with free L-cysteine); phosphorylated residue; monohydroxylated residue |
| Instrument | Q Exactive |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
|---|---|---|---|
| 0 | 2025-02-23 15:59:21 | ID requested | |
| ⏵ 1 | 2026-06-07 17:10:41 | announced |
Publication List
| 10.1016/j.mcpro.2026.101560; |
| 10.6019/PXD061101; |
| Mecklenbr, ä, uker S, Skoczylas P, Biernat P, Zaghla BKQ, Atay B, Hossam M, Kr, ó, l-J, ó, zaga B, Jasi, ń, ski M, Pienkowski VM, Sanecka-Duin A, Popp O, Haji M, Szatanek R, Mertins P, Kaczmarczyk J, Keller U, Blum A, Klatt MG, Identification of MHC Ligands Through Allele-Guided Isolation Combined With Machine Learning for Improved MHC Assignment Using ARDisplay-I. Mol Cell Proteomics, 25(5):101560(2026) [pubmed] |
Keyword List
| submitter keyword: HLA assignment, Machine Learning,Immunopeptidome |
Contact List
| Martin Klatt | |
|---|---|
| contact affiliation | Charité-University Medicine Berlin |
| contact email | martin.klatt@charite.de |
| lab head | |
| Martin Klatt | |
| contact affiliation | Charite - University Medicine Berlin |
| contact email | martin.g.klatt@gmail.com |
| 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/2026/06/PXD061101 |
| PRIDE project URI |
Repository Record List
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