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1000 Titel
  • Use of antibodies against Epstein–Barr virus nuclear antigen 1 for detection of cellular proteins with monomethylated arginine residues that are potentially involved in viral transformation
1000 Autor/in
  1. Graesser, Christian |
  2. Nord, Ruth |
  3. Flaswinkel, Heinrich |
  4. Kremmer, Elisabeth |
  5. Meese, Eckart |
  6. Caban, Karolina Magdalena |
  7. Fröhlich, Thomas |
  8. Grässer, Friedrich A. |
  9. Hart, Martin |
1000 Verlag
  • Springer Vienna
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-11-08
1000 Erschienen in
1000 Quellenangabe
  • 169(12):241
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00705-024-06172-7 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11549202/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:p>Epstein–Barr virus nuclear antigen 1 (EBNA1) contains two arginine-glycine (RG) repeats that contain symmetric/asymmetric dimethylarginine (SDMA/ADMA) and monomethylarginine (MMA) residues. We generated mouse monoclonal antibodies directed against a monomethylated GRGRGG-containing repeat located between amino acids 328 and 377 of EBNA1. In addition to detecting MMA-modified EBNA1, we also had the goal of identifying cellular proteins that bind to MMA-modified EBNA1 in EBV-positive Raji cells. Furthermore, we hypothesized that antibodies against MMA-modified EBNA1 might also recognize cell factors that use an MMA-modified surface structure similar to that of EBNA1 to bind to their common targets. Using a combination of immunoprecipitation and mass spectrometry, we identified a number of such cellular proteins, including SNRPD1-3, ALY/REF, RPS15, DIDO1, LSM12, LSM14A, DAP3, and CPSF1. An NACA complex protein that was shown previously to bind to the glycine-alanine repeat of EBNA1 was also identified. The proteins identified in this study are involved in splicing, tumorigenesis, transcriptional activation, DNA stability, and RNA processing or export.</jats:p>
1000 Sacherschließung
lokal Epstein-Barr Virus Nuclear Antigens/genetics [MeSH]
lokal Antibodies, Monoclonal/immunology [MeSH]
lokal Humans [MeSH]
lokal Epstein-Barr Virus Nuclear Antigens/immunology [MeSH]
lokal Herpesvirus 4, Human/immunology [MeSH]
lokal Animals [MeSH]
lokal Mice [MeSH]
lokal Brief Report
lokal Arginine/chemistry [MeSH]
lokal Epstein-Barr Virus Nuclear Antigens/chemistry [MeSH]
lokal Herpesvirus 4, Human/genetics [MeSH]
lokal Cell Transformation, Viral [MeSH]
lokal Arginine/metabolism [MeSH]
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/R3JhZXNzZXIsIENocmlzdGlhbg==|https://frl.publisso.de/adhoc/uri/Tm9yZCwgUnV0aA==|https://frl.publisso.de/adhoc/uri/Rmxhc3dpbmtlbCwgSGVpbnJpY2g=|https://frl.publisso.de/adhoc/uri/S3JlbW1lciwgRWxpc2FiZXRo|https://frl.publisso.de/adhoc/uri/TWVlc2UsIEVja2FydA==|https://frl.publisso.de/adhoc/uri/Q2FiYW4sIEthcm9saW5hIE1hZ2RhbGVuYQ==|https://frl.publisso.de/adhoc/uri/RnLDtmhsaWNoLCBUaG9tYXM=|https://frl.publisso.de/adhoc/uri/R3LDpHNzZXIsIEZyaWVkcmljaCBBLg==|https://orcid.org/0000-0001-9361-8106
1000 Hinweis
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1000 Förderer
  1. Universität des Saarlandes |
1000 Fördernummer
  1. -
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1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Universität des Saarlandes |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 @id frl:6524508.rdf
1000 Erstellt am 2025-07-07T04:54:10.338+0200
1000 Erstellt von 322
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1000 Zuletzt bearbeitet 2025-07-30T01:14:20.444+0200
1000 Objekt bearb. Wed Jul 30 01:14:20 CEST 2025
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