Research Topics
| DEBI NAYAKSummaryAffiliation: University of California Country: USA Publications
Research Grants
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Publications
Influenza virus morphogenesis and buddingDebi P Nayak
Department of Microbiology, Immunology and Molecular Genetics, Molecular Biology Institute, Jonsson Comprehensive Cancer Center, David Geffen School of Medicine, University of California at Los Angeles, Los Angeles, CA 90095, USA
Virus Res 143:147-61. 2009..We provide our current understanding of these important processes leading to the production of infectious influenza virus particles...
Assembly and budding of influenza virusDebi P Nayak
Department of Microbiology, Immunology and Molecular Genetics, Jonsson Comprehensive Cancer Center, Molecular Biology Institute, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA
Virus Res 106:147-65. 2004..Elucidation of both viral and host factors involved in viral morphogenesis and budding may lead to the development of drugs interfering with the steps of viral morphogenesis and in disease progression...
D-4F, an apolipoprotein A-I mimetic peptide, inhibits the inflammatory response induced by influenza A infection of human type II pneumocytesBrian J Van Lenten
Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, Calif 90095 1679, USA
Circulation 110:3252-8. 2004..We previously reported that an apoA-I mimetic peptide, D-4F, reduced inflammatory responses to influenza virus in mice. To further define the antiinflammatory activity of D-4F, a human alveolar type II cell line, A549, was used...
Influenza infection promotes macrophage traffic into arteries of mice that is prevented by D-4F, an apolipoprotein A-I mimetic peptideBrian J Van Lenten
Department of Medicine, UCLA School of Medicine, University of California at Los Angeles, 90095 1679, USA
Circulation 106:1127-32. 2002..The present study tested this hypothesis...
Basic residues of the helix six domain of influenza virus M1 involved in nuclear translocation of M1 can be replaced by PTAP and YPDL late assembly domain motifsEric Ka-Wai Hui
Department of Microbiology, Immunology and Molecular Genetics, Jonsson Comprehensive Cancer Center, Molecular Biology Institute, UCLA School of Medicine, Los Angeles, California 90095-1747, USA
J Virol 77:7078-92. 2003..Furthermore, these sequences of H6 domain can be replaced by late (L) domain motifs and therefore may provide a function similar to that of the L domains of other negative-strand RNA and retroviruses...
Mutations in influenza virus M1 CCHH, the putative zinc finger motif, cause attenuation in mice and protect mice against lethal influenza virus infectionEric Ka-Wai Hui
Department of Microbiology, Immunology, and Molecular Genetics, Jonsson Comprehensive Cancer Center, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095-1747, USA
J Virol 80:5697-707. 2006....
Inhibition of influenza virus matrix (M1) protein expression and virus replication by U6 promoter-driven and lentivirus-mediated delivery of siRNAEric Ka-Wai Hui
Department of Microbiology, Molecular Biology Institute, David Geffen School of Medicine, UCLA, Los Angeles, CA 90095, USA
J Gen Virol 85:1877-84. 2004..Therefore, lentivirus-mediated delivery of siRNA and gene silencing can be used in studying the specific functions of virus genes in replication and may have a potential therapeutic application...
Influenza A virus hemagglutinin containing basolateral localization signal does not alter the apical budding of a recombinant influenza A virus in polarized MDCK cellsSubrata Barman
Department of Microbiology, Immunology, and Molecular Genetics, Molecular Biology Institute, UCLA School of Medicine, Los Angeles, California 90095-1747, USA
Virology 305:138-52. 2003..Therefore HA, the major glycoprotein alone, does not determine the budding site, and other factor(s), possibly both viral and host, is responsible for selecting the budding site of influenza virus...
Conserved cysteine and histidine residues in the putative zinc finger motif of the influenza A virus M1 protein are not critical for influenza virus replicationEric Ka-Wai Hui
Department of Microbiology, Immunology and Molecular Genetics, Jonsson Comprehensive Cancer Center, Molecular Biology Institute, UCLA School of Medicine, Los Angeles, CA 90095, USA
J Gen Virol 84:3105-13. 2003..However, the lethal phenotype of the Ala(155) mutation shows that the H9 region of M1 provides some other critical function(s) in virus replication...
Role of lipid rafts in virus assembly and buddingDebi P Nayak
Department of Microbiology, Immunology and Molecular Genetics, UCLA School of Medicine, Molecular Biology Institute, Los Angeles, California 90095-1747, USA
Adv Virus Res 58:1-28. 2002
Role of G protein and protein kinase signalling in influenza virus budding in MDCK cellsEric Ka-Wai Hui
Department of Microbiology, Immunology and Molecular Genetics, Jonsson Comprehensive Cancer Center (JCCC, UCLA School of Medicine, Los Angeles, CA 90095-1747, USA
J Gen Virol 83:3055-66. 2002..Also, in digitonin-permeabilized MDCK cells, the introduction of CK2 substrate peptides caused a down-regulation of virus budding. These results suggest that CK2 activity also regulates influenza virus budding...
YRKL sequence of influenza virus M1 functions as the L domain motif and interacts with VPS28 and Cdc42Eric Ka Wai Hui
Department of Microbiology, Immunology and Molecular Genetics, Jonsson Comprehensive Cancer Center, Molecular Biology Institute, David Geffen School of Medicine, UCLA, Los Angeles, 90095, USA
J Virol 80:2291-308. 2006..These results indicated that VPS28, a component of ESCRT-I, and Cdc42, a small G protein, are associated with the M1 protein and involved in the influenza virus life cycle...
Lipid raft disruption by cholesterol depletion enhances influenza A virus budding from MDCK cellsSubrata Barman
Department of Microbiology, Immunology and Molecular Genetics, Jonsson Comprehensive Cancer Center, Molecular Biology Institute, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095 1747, USA
J Virol 81:12169-78. 2007..These data show that disruption of lipid rafts by cholesterol depletion caused an enhancement of virus particle release from infected cells and a decrease in the infectivity of virus particles...
Role of transmembrane domain and cytoplasmic tail amino acid sequences of influenza a virus neuraminidase in raft association and virus buddingSubrata Barman
Department of Microbiology, Immunology, and Molecular Genetics, Molecular Biology Institute, University of California-Los Angeles School of Medicine, Los Angeles, CA 90095-1747, USA
J Virol 78:5258-69. 2004..In addition, aberrant morphogenesis including elongated particle formation of some mutant viruses indicates the involvement of NA in virus morphogenesis and budding...
Research Grants
- INTERFERENCE BY DEFECTIVE INFLUENZA VIRUSESDEBI NAYAK; Fiscal Year: 2001..what are the functions of nucleocapsid protein (NP) in modulating the polymerase activity, and 5. what are the requirements of type (A, B, and C) specificity for viral polymerases? ..
- CLONING AND EXPRESSION OF INFLUENZA VIRAL RNA SEGMENTSDEBI NAYAK; Fiscal Year: 2005..A detailed understanding of these processes will facilitate the rational development of antiviral agents which could interfere with one or more steps in virus assembly. ..
- CLONING OF INFLUENZA VIRAL RNA SEGMENTSDEBI NAYAK; Fiscal Year: 1980..Finally using E. coli promotor, we hope to synthesize major viral antigens (hemagglutinin and neuraminidase) which may provide a better immunogen(s) against influenza...
- CLONING AND EXPRESSION OF INFLUENZA VIRAL RNA SEGMENTSDEBI NAYAK; Fiscal Year: 1992..In addition, we are expressing influenza viral HA and NA in yeast (Saccharomyces cerevisiae), which may be of potential use in the development of an improved subunit vaccine...
- INTERFERENCE BY DEFECTIVE INFLUENZA VIRUSESDEBI NAYAK; Fiscal Year: 2007..abstract_text> ..
