PXD052028-1
PXD052028 is an original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Development of a high-throughput (10 minute microflow gradient) platform for quantitation of histone modifications on a new QTOF instrument |
| Description | Histone post-translational modifications (PTMs) regulate gene expression patterns through epigenetic mechanisms. The 5 histone proteins (H1, H2A, H2B, H3, and H4) are extensively modified, with over 75 distinct modification types spanning more than 200 sites. Despite strong advances in mass spectrometry based approaches, identification and quantification of modified histone peptides remains challenging due to factors such as isobaric peptides, pseudo-isobaric PTMs, and low stoichiometry of certain marks. Here we describe the development of a new high-throughput method to identify and quantitate over 150 modified histone peptides by liquid chromatography-mass spectrometry (LC-MS). Fast gradient microflow liquid chromatography and variable window SWATH data-independent acquisition on a new quadrupole time-of-flight platform is compared to a previous method using nanoflow LC-MS on an Orbitrap hybrid instrument. Histones extracted from cells treated with either a histone deacetylase inhibitor (HDACi) or TGF-beta 1 were analyzed by data-independent acquisition (DIA) on two mass spectrometers: an Orbitrap Exploris 240 with a 55 minute nanoflow LC gradient, and the SCIEX ZenoTOF 7600 with 5 and 10 minute microflow gradients, with data analyzed using newly developed in-house software. To demonstrate the reproducibility and speed advantage of the method, 100 consecutive injections of one sample were performed in less than 2 days on the QTOF platform. The result is the comprehensive characterization of histone PTMs achieved in less than 20 minutes of total run time using only 200 ng of sample. Results for histone PTMs extracted from cells treated with epigenetic drugs or undergoing cellular transformation are comparable to those produced by the previous method, but can be achieved using less than one-third of the instrument time and one-fifth of the sample amount. |
| HostingRepository | MassIVE |
| AnnounceDate | 2025-07-01 |
| AnnouncementXML | Submission_2025-07-01_08:04:14.650.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Emily Zahn |
| SpeciesList | scientific name: Homo sapiens; common name: human; NCBI TaxID: 9606; |
| ModificationList | Methyl; Dimethyl; Trimethyl; Acetyl; Phospho |
| Instrument | Orbitrap Exploris 240 |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
|---|---|---|---|
| 0 | 2024-05-06 14:26:35 | ID requested | |
| ⏵ 1 | 2025-07-01 08:04:15 | announced |
Publication List
| Zahn E, Xie Y, Liu X, Karki R, Searfoss RM, de Luna Vitorino FN, Lempi, รค, inen JK, Gongora J, Lin Z, Zhao C, Yuan ZF, Garcia BA, Development of a High-Throughput Platform for Quantitation of Histone Modifications on a New QTOF Instrument. Mol Cell Proteomics, 24(1):100897(2025) [pubmed] |
Keyword List
| submitter keyword: epigenetics |
Contact List
| Benjamin A. Garcia | |
|---|---|
| contact affiliation | Washington University School of Medicine in St. Louis |
| contact email | bagarcia@wustl.edu |
| lab head | |
| Emily Zahn | |
| contact affiliation | Washington University School of Medicine |
| contact email | zahn@wustl.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-ftp.ucsd.edu/v07/MSV000094695/ |
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