Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1993-2-17
pubmed:abstractText
Cell lines stably releasing noninfectious virus-like particles containing wild type or mutant gene products represent useful tools for a biochemical, immunological, and structural analysis of virus assembly. Human immunodeficiency virus (HIV) type 1 gag and env gene products were transiently and stably expressed in mammalian cells and the formation of virus-like particles incorporating viral glycoproteins was analyzed. Transient cotransfection of plasmids directing the synthesis of gag and env gene products yielded efficient release of particles but specific incorporation of HIV glycoproteins was not detected. A stable cell line expressing wild type HIV-1 glycoproteins was generated and transient transfection of this cell line with gag-encoding constructs led to the release of virus-like particles incorporating HIV surface and transmembrane glycoproteins. Attempts to establish stable cell lines expressing wild type HIV gag and pol genes were unsuccessful and only highly unstable lines primarily expressing uncleaved precursor polyproteins were obtained. This result appears to be caused by the cytotoxic effects of the viral proteinase since stable lines were readily selected after transfection of constructs either encoding an inactive mutant of the proteinase or a mutated frameshift signal which prevented expression of the pol reading frame. Stable coexpression of uncleaved Gag polyprotein and wild type env gene products yielded efficient release of immature virus-like particles incorporating HIV glycoproteins. Electron micrographs revealed lentiviral budding structures with the typical surface projections of viral glycoprotein oligomers.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0042-6822
pubmed:author
pubmed:issnType
Print
pubmed:volume
192
pubmed:geneSymbol
env, gag
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
605-17
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:8421902-Animals, pubmed-meshheading:8421902-Base Sequence, pubmed-meshheading:8421902-Blotting, Western, pubmed-meshheading:8421902-Cell Line, pubmed-meshheading:8421902-DNA, Viral, pubmed-meshheading:8421902-Fluorescent Antibody Technique, pubmed-meshheading:8421902-Gene Products, env, pubmed-meshheading:8421902-Gene Products, gag, pubmed-meshheading:8421902-Genes, env, pubmed-meshheading:8421902-Genes, gag, pubmed-meshheading:8421902-HIV Protease, pubmed-meshheading:8421902-HIV-1, pubmed-meshheading:8421902-Microscopy, Electron, pubmed-meshheading:8421902-Molecular Sequence Data, pubmed-meshheading:8421902-Molecular Weight, pubmed-meshheading:8421902-Mutagenesis, Site-Directed, pubmed-meshheading:8421902-Plasmids, pubmed-meshheading:8421902-Recombinant Fusion Proteins, pubmed-meshheading:8421902-Transfection
pubmed:year
1993
pubmed:articleTitle
Analysis of protein expression and virus-like particle formation in mammalian cell lines stably expressing HIV-1 gag and env gene products with or without active HIV proteinase.
pubmed:affiliation
Angewandte Tumorvirologie, Deutsches Krebsforschungszentrum, Heidelberg.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't