Three Variations in the Cell Surface Expression of the Haemagglutinin-Neuraminidase Glycoprotein of Sendai Virus
- 1 May 1985
- journal article
- research article
- Published by Microbiology Society in Journal of General Virology
- Vol. 66 (5), 987-1000
- https://doi.org/10.1099/0022-1317-66-5-987
Abstract
The fate of the hemagglutinin-neuraminidase glycoprotein (HN) of Sendai virus in 3 types of infection was studied by measuring its sensitivity to endoglycosidase H and its rate of appearance and turnover at the cell surface. HN behaved differently in the 3 types of infection. When highly expressed at the surface, as in a lytic standard virus infection, HN accumulated at the surface in a stable form (half-life of disappearance from the surface .mchgt. 10 h). When moderately expressed, as in a non-lytic standard virus plus defective interfering virus infection, HN reached the membrane normally, but turned over rapidly (half-life .apprx. 2 h) and was re-internalized. When poorly expressed, as in long-term persistent infection, HN did not reach the cell surface and appeared to be degraded before reaching it. In contrast to HN, the other viral glycoprotein, Fo, exhibited a similar turnover rate at the cell surface in the 3 situations. However, when compared to surface expression in standard virus-infected cells under standardized conditions, Fo surface expression in persistently infected cells was reduced. This reduction correlates with a decreased maturation rate in these cells.This publication has 19 references indexed in Scilit:
- Establishment of Sendai virus persistent infection: Biochemical analysis of the early phase of a standard plus defective interfering virus infection of BHK cellsVirology, 1981
- Carbohydrate structures of HVJ (Sendai virus) glycoproteins.Journal of Biological Chemistry, 1981
- Intracellular transport of secretory and membrane proteins in hepatoma cells infected by vesicular stomatitis virusCell, 1980
- Alterations in expression of measles virus polypeptides by antibody: molecular events in antibody-induced antigenic modulation.The Journal of Immunology, 1980
- Virus protein changes and RNA termini alterations evolving during persistent infectionCell, 1980
- Role of defective interfering particles of sendai virus in persistent infectionsVirology, 1979
- Carbohydrate composition of the envelope glycoproteins of Sendai virusVirology, 1978
- Proposal for a common oligosaccharide intermediate in the synthesis of membrane glycoproteinsCell, 1977
- The substrate specificities of endo-β-N-acetylglucosaminidases CII and HBiochemical and Biophysical Research Communications, 1977
- Isolation and characterization of Sendai virus DI-RNAsCell, 1976