Normal human cell proteins that interact with the adenovirus type 5 E1B 55 kDa protein

George Hung, S. J. Flint

Research output: Contribution to journalArticle

5 Scopus citations

Abstract

Several of the functions of the human adenovirus type 5 E1B 55 kDa protein are fulfilled via the virus-specific E3 ubiquitin ligase it forms with the viral E4 Orf6 protein and several cellular proteins. Important substrates of this enzyme have not been identified, and other functions, including repression of transcription of interferon-sensitive genes, do not require the ligase. We therefore used immunoaffinity purification and liquid chromatography-mass spectrometry of lysates of normal human cells infected in parallel with HAdV-C5 and E1B 55 kDa protein-null mutant viruses to identify specifically E1B 55 kDa-associated proteins. The resulting set of >90 E1B-associated proteins contained the great majority identified previously, and was enriched for those associated with the ubiquitin-proteasome system, RNA metabolism and the cell cycle. We also report very severe inhibition of viral genome replication when cells were exposed to both specific or non-specific siRNAs and interferon prior to infection.

Original languageEnglish (US)
Pages (from-to)12-24
Number of pages13
JournalVirology
Volume504
DOIs
StatePublished - Apr 1 2017

All Science Journal Classification (ASJC) codes

  • Virology

Keywords

  • E1B 55 kDa protein
  • Human adenovirus type 5 (HAdV-C5)
  • Mass spectrometry
  • Normal human cells
  • RNA metabolism
  • Type I interferons
  • Ubiquitin-proteasome system

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