Normal human cell proteins that interact with the adenovirus type 5 E1B 55kDa protein. Author George Hung, S Flint Publication Year 2017 Type Journal Article Abstract Several of the functions of the human adenovirus type 5 E1B 55kDa 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 55kDa protein-null mutant viruses to identify specifically E1B 55kDa-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. Keywords Repressor Proteins, RNA-Binding Proteins, Nuclear Proteins, Humans, HeLa Cells, Amino Acid Sequence, HEK293 Cells, Virus Replication, RNA Interference, RNA, Small Interfering, Adenovirus E4 Proteins, Adenovirus E1B Proteins, Adenoviruses, Human, DNA, Viral, Genome, Viral, Intracellular Signaling Peptides and Proteins, A549 Cells, Sin3 Histone Deacetylase and Corepressor Complex Journal Virology Volume 504 Pages 12-24 Date Published 2017 Apr ISSN Number 1096-0341 DOI 10.1016/j.virol.2017.01.013 Alternate Journal Virology PMCID PMC5337154 PMID 28135605 PubMedPubMed CentralGoogle ScholarBibTeXEndNote X3 XML