Home LiteratureArticle Details
PMID: 8421902 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

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.

Virology ·Vol. 192 ·No. 2 ·1993-02-00 ·Pages 605-17

Kräusslich HG, Ochsenbauer C, Traenckner AM, Mergener K, Fäcke M, Gelderblom HR, Bosch V

Abstract

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.

Related Genes
MeSH Terms
Animals Base Sequence Blotting, Western Cell Line DNA, Viral/genetics Fluorescent Antibody Technique Gene Products, env/analysis,biosynthesis,genetics Gene Products, gag/analysis,biosynthesis,genetics Genes, env Genes, gag HIV Protease/genetics,metabolism HIV-1/genetics,metabolism,ultrastructure Microscopy, Electron Molecular Sequence Data Molecular Weight Mutagenesis, Site-Directed Plasmids Recombinant Fusion Proteins/analysis,biosynthesis Transfection
Chemicals
DNA, Viral Gene Products, env Gene Products, gag Recombinant Fusion Proteins HIV Protease
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Kräusslich H G
Angewandte Tumorvirologie, Deutsches Krebsforschungszentrum, Heidelberg.
Ochsenbauer C
Traenckner A M
Mergener K
Fäcke M
Gelderblom H R
Bosch V
Article Info
Journal
Virology
Abbr.
Virology
ISSN
0042-6822
Published
1993-02-00
Pages
605-17
Language
English
Region
United States
NLM ID
0110674
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]