PXD052584 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Cross-linking MS supporting: Structural stabilization of the intrinsically disordered SARS-CoV-2 N by binding to RNA sequences engineered from the viral genome |
| Description | The nucleocapsid N is one of four structural proteins of the coronaviruses. Its essential role in genome encapsidation makes it a critical therapeutic target for COVID-19 and related diseases. However, the inherent disorder of full-length N has hampered its structural analysis. Here, we describe a stepwise method using viral-derived RNAs to stabilize SARS-CoV-2 N for EM analysis. We identified pieces of RNA from the SARS-CoV-2 genome that promote the formation of structurally homogeneous N dimers, intermediates of assembly, and filamentous capsid-like structures. Building on these results, we engineered a symmetric RNA to stabilize N protein dimers, the building block of high-order assemblies, for EM analyses. We combined domain-specific monoclonal antibodies against N with chemical cross-linking mass spectrometry and cryo-EM to validate the atomic model for the N dimer. The resulting N dimer structure provides insights into its architectural and antigenic principles, which can guide design of pan-coronavirus therapeutics. |
| HostingRepository | PRIDE |
| AnnounceDate | 2025-07-21 |
| AnnouncementXML | Submission_2025-07-20_16:06:59.842.xml |
| DigitalObjectIdentifier | https://dx.doi.org/10.6019/PXD052584 |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Supported dataset by repository |
| PrimarySubmitter | Andrew Norris |
| SpeciesList | scientific name: Severe acute respiratory syndrome coronavirus 2; NCBI TaxID: 2697049; |
| ModificationList | No PTMs are included in the dataset |
| Instrument | Orbitrap Fusion |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2024-05-27 03:35:30 | ID requested | |
| ⏵ 1 | 2025-07-20 16:07:00 | announced | |
Publication List
| 10.1038/s41467-025-61861-4; |
| 10.6019/PXD052584; |
| Landeras-Bueno S, Hariharan C, Avalos RD, Norris AS, Snyder DT, Hastie KM, Harkins S, Zandonatti M, Rajamanickam RR, Olmedillas E, Miller R, Shresta S, Wysocki VH, Saphire EO, Structural stabilization of the intrinsically disordered SARS-CoV-2 N by binding to RNA sequences engineered from the viral genome fragment. Nat Commun, 16(1):6521(2025) [pubmed] |
Keyword List
| submitter keyword: cross-linking,XL-MS, SARS-CoV-2 N |
Contact List
| Vicki H. Wysocki |
| contact affiliation | Department of Chemistry and Biochemistry, The Ohio State University, Columbus, OH 14 43210, USA |
| contact email | wysocki.11@osu.edu |
| lab head | |
| Andrew Norris |
| contact affiliation | The Ohio State University |
| contact email | norris942@gmail.com |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
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| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD052584
- Label: PRIDE project
- Name: Cross-linking MS supporting: Structural stabilization of the intrinsically disordered SARS-CoV-2 N by binding to RNA sequences engineered from the viral genome