PXD022282 is an 
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Multi-level proteomics reveals host-perturbation strategies of SARS-CoV-2 and SARS-CoV | 
| Description | The  sudden  global  emergence  of  SARS-CoV-2  urgently  requires  an  in-depth  understanding  of  molecular  functions  of  viral  proteins  and  their  interactions  with  the  host  proteome.  Several  omics  studies  have  extended  our  knowledge  of  COVID-19  pathophysiology,  including  some  focused  on  proteomic aspects1–3. To understand how SARS-CoV-2 and related coronaviruses manipulate the host we here characterized interactome, proteome and signaling processes in a systems-wide manner. This identified  connections  between  the  corresponding  cellular  events,  revealed  functional  effects  of  the  individual  viral  proteins  and  put  these  findings  into  the  context  of  host  signaling  pathways.  We  investigated  the  closely  related  SARS-CoV-2  and  SARS-CoV  viruses  as  well  as  the  influence  of  SARS-CoV-2  on  transcriptome,  proteome,  ubiquitinome  and  phosphoproteome  of  a  lung-derived  human  cell  line.  Projecting  these  data  onto  the  global  network  of  cellular  interactions  revealed  relationships  between  the  perturbations  taking  place  upon  SARS-CoV-2  infection  at  different  layers  and  identified  unique  and  common  molecular  mechanisms  of  SARS  coronaviruses.  The  results  highlight  the  functionality  of  individual  proteins  as  well  as  vulnerability  hotspots  of  SARS-CoV-2,  which  we  targeted  with  clinically  approved  drugs.  We exemplify  this  by  identification  of  kinase  inhibitors as well as MMPase inhibitors with significant antiviral effects against SARS-CoV-2. | 
| HostingRepository | PRIDE | 
| AnnounceDate | 2024-10-22 | 
                | AnnouncementXML | Submission_2024-10-22_05:18:54.466.xml | 
                | DigitalObjectIdentifier |  | 
| ReviewLevel | Peer-reviewed dataset | 
| DatasetOrigin | Original dataset | 
| RepositorySupport | Unsupported dataset by repository | 
| PrimarySubmitter | Mario Oroshi | 
| SpeciesList |  scientific name: Homo sapiens (Human);  NCBI TaxID: 9606;  scientific name: Saccharomyces cerevisiae (Baker's yeast);  NCBI TaxID: 4932;  | 
| ModificationList | ubiquitinylated lysine; phosphorylated residue | 
| Instrument | Orbitrap Exploris 480 | 
Dataset History
| Revision | Datetime | Status | ChangeLog Entry | 
| 0 | 2020-11-02 00:18:37 | ID requested |  | 
| 1 | 2021-02-15 04:04:33 | announced |  | 
| ⏵ 2 | 2024-10-22 05:18:54 | announced | 2024-10-22: Updated project metadata. | 
Publication List 
| Dataset with its publication pending | 
Keyword List 
| ProteomeXchange project tag: Sars-cov-2, Covid-19 | 
| submitter keyword: proteomics,COVID19, DIA, mass spectrometry, PTM, SARS-CoV-2, ubiquitination, phosphorylation, LC-MS/MS | 
Contact List 
| Matthias Mann | 
| contact affiliation | Department of Proteomics and Signal Transduction, Max Planck Institute of Biochemistry, 82152 Martinsried, Germany | 
| contact email | mmann@biochem.mpg.de | 
| lab head |  | 
| Mario Oroshi | 
| contact affiliation | Proteomics | 
| contact email | oroshi@biochem.mpg.de | 
| 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/2021/02/PXD022282 | 
| PRIDE project URI | 
		 Repository Record List 
                 [ + ]
		 [ - ]
		 
        - PRIDE
- PXD022282
- Label: PRIDE project
 - Name: Multi-level proteomics reveals host-perturbation strategies of SARS-CoV-2 and SARS-CoV