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  • 1
    Publication Date: 2000-11-25
    Description: The endoplasmic reticulum (ER) supports disulfide bond formation by a poorly understood mechanism requiring protein disulfide isomerase (PDI) and ERO1. In yeast, Ero1p-mediated oxidative folding was shown to depend on cellular flavin adenine dinucleotide (FAD) levels but not on ubiquinone or heme, and Ero1p was shown to be a FAD-binding protein. We reconstituted efficient oxidative folding in vitro using FAD, PDI, and Ero1p. Disulfide formation proceeded by direct delivery of oxidizing equivalents from Ero1p to folding substrates via PDI. This kinetic shuttling of oxidizing equivalents could allow the ER to support rapid disulfide formation while maintaining the ability to reduce and rearrange incorrect disulfide bonds.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Tu, B P -- Ho-Schleyer, S C -- Travers, K J -- Weissman, J S -- New York, N.Y. -- Science. 2000 Nov 24;290(5496):1571-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute, Department of Cellular and Molecular Pharmacology, University of California, San Francisco, CA 94143, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/11090354" target="_blank"〉PubMed〈/a〉
    Keywords: Binding Sites ; Carboxypeptidases/chemistry/metabolism ; Cathepsin A ; Chemistry, Physical ; Disulfides/chemistry ; Endoplasmic Reticulum/*metabolism ; Flavin-Adenine Dinucleotide/*metabolism ; Glutathione/metabolism ; Glycoproteins/*metabolism ; Microsomes/metabolism ; Mutation ; Oxidation-Reduction ; Oxidoreductases Acting on Sulfur Group Donors ; Physicochemical Phenomena ; Protein Disulfide-Isomerases/genetics/*metabolism ; *Protein Folding ; Ribonuclease, Pancreatic/chemistry/metabolism ; Saccharomyces cerevisiae/metabolism ; *Saccharomyces cerevisiae Proteins
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2009-12-23
    Description: Influenza A virus is an RNA virus that encodes up to 11 proteins and this small coding capacity demands that the virus use the host cellular machinery for many aspects of its life cycle. Knowledge of these host cell requirements not only informs us of the molecular pathways exploited by the virus but also provides further targets that could be pursued for antiviral drug development. Here we use an integrative systems approach, based on genome-wide RNA interference screening, to identify 295 cellular cofactors required for early-stage influenza virus replication. Within this group, those involved in kinase-regulated signalling, ubiquitination and phosphatase activity are the most highly enriched, and 181 factors assemble into a highly significant host-pathogen interaction network. Moreover, 219 of the 295 factors were confirmed to be required for efficient wild-type influenza virus growth, and further analysis of a subset of genes showed 23 factors necessary for viral entry, including members of the vacuolar ATPase (vATPase) and COPI-protein families, fibroblast growth factor receptor (FGFR) proteins, and glycogen synthase kinase 3 (GSK3)-beta. Furthermore, 10 proteins were confirmed to be involved in post-entry steps of influenza virus replication. These include nuclear import components, proteases, and the calcium/calmodulin-dependent protein kinase (CaM kinase) IIbeta (CAMK2B). Notably, growth of swine-origin H1N1 influenza virus is also dependent on the identified host factors, and we show that small molecule inhibitors of several factors, including vATPase and CAMK2B, antagonize influenza virus replication.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2862546/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2862546/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Konig, Renate -- Stertz, Silke -- Zhou, Yingyao -- Inoue, Atsushi -- Hoffmann, H-Heinrich -- Bhattacharyya, Suchita -- Alamares, Judith G -- Tscherne, Donna M -- Ortigoza, Mila B -- Liang, Yuhong -- Gao, Qinshan -- Andrews, Shane E -- Bandyopadhyay, Sourav -- De Jesus, Paul -- Tu, Buu P -- Pache, Lars -- Shih, Crystal -- Orth, Anthony -- Bonamy, Ghislain -- Miraglia, Loren -- Ideker, Trey -- Garcia-Sastre, Adolfo -- Young, John A T -- Palese, Peter -- Shaw, Megan L -- Chanda, Sumit K -- 1 P01 AI058113/AI/NIAID NIH HHS/ -- 1 S10 RR0 9145-01/RR/NCRR NIH HHS/ -- 1 T32 AI07647/AI/NIAID NIH HHS/ -- 1F32AI081428/AI/NIAID NIH HHS/ -- 1R21AI083673/AI/NIAID NIH HHS/ -- 5R24 CA095823-04/CA/NCI NIH HHS/ -- HHSN266200700010C/PHS HHS/ -- HHSN272200900032C/PHS HHS/ -- P01 AI058113/AI/NIAID NIH HHS/ -- P01 AI058113-010004/AI/NIAID NIH HHS/ -- P01 AI058113-020004/AI/NIAID NIH HHS/ -- P01 AI058113-030004/AI/NIAID NIH HHS/ -- P01 AI058113-040004/AI/NIAID NIH HHS/ -- P01 AI058113-050004/AI/NIAID NIH HHS/ -- T32 AI007647/AI/NIAID NIH HHS/ -- T32 AI007647-01/AI/NIAID NIH HHS/ -- T32 AI007647-02/AI/NIAID NIH HHS/ -- T32 AI007647-03/AI/NIAID NIH HHS/ -- T32 AI007647-04/AI/NIAID NIH HHS/ -- T32 AI007647-05/AI/NIAID NIH HHS/ -- T32 AI007647-06/AI/NIAID NIH HHS/ -- T32 AI007647-07/AI/NIAID NIH HHS/ -- T32 AI007647-08/AI/NIAID NIH HHS/ -- T32 AI007647-09/AI/NIAID NIH HHS/ -- T32 AI007647-10/AI/NIAID NIH HHS/ -- T32 GM007280/GM/NIGMS NIH HHS/ -- U01 AI074539/AI/NIAID NIH HHS/ -- U01 AI074539-01/AI/NIAID NIH HHS/ -- U01 AI074539-02/AI/NIAID NIH HHS/ -- U01 AI074539-03/AI/NIAID NIH HHS/ -- U01 AI1074539/AI/NIAID NIH HHS/ -- U54 AI057158/AI/NIAID NIH HHS/ -- U54 AI057158-065713/AI/NIAID NIH HHS/ -- U54 AI057159/AI/NIAID NIH HHS/ -- England -- Nature. 2010 Feb 11;463(7282):813-7. doi: 10.1038/nature08699.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Infectious and Inflammatory Disease Center, Burnham Institute for Medical Research.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/20027183" target="_blank"〉PubMed〈/a〉
    Keywords: Animals ; Biological Factors/*genetics/*physiology ; Cell Line ; Cercopithecus aethiops ; Gene Library ; Genome, Human/genetics ; Host-Pathogen Interactions/genetics/*physiology ; Humans ; Influenza A Virus, H1N1 Subtype/classification/growth & development ; Influenza A virus/classification/*growth & development ; Influenza, Human/*genetics/*virology ; RNA Interference ; Vero Cells ; Virus Internalization ; Virus Replication/*physiology
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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