Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1984 Feb;49(2):594-7.
doi: 10.1128/JVI.49.2.594-597.1984.

Virus-specific glycoproteins associated with the nuclear fraction of herpes simplex virus type 1-infected cells

Virus-specific glycoproteins associated with the nuclear fraction of herpes simplex virus type 1-infected cells

T Compton et al. J Virol. 1984 Feb.

Abstract

Monospecific antisera to herpes simplex virus type 1 (HSV-1) glycoproteins gB, gC, and gD were used to identify the HSV-1-specific glycoproteins associated with the nuclear fraction as compared with those associated with cytoplasmic fraction, whole-cell lysates, and purified virions. The results indicate that a predominance of HSV glycoprotein precursors pgC(105), pgB(110), and pgD(52) is associated with the nuclear fraction. Treatment of the nuclear fraction with the enzyme endo-beta-N-acetylglucosaminidase H indicated that the lower-molecular-weight glycoproteins are sensitive to this endoglycosidase. These results suggest that in the nuclear fraction of HSV-1-infected cells virus-specific glycoproteins gB, gC, and gD are predominately in the high-mannose precursor form; however, detectable amounts of the fully glycosylated forms of gC and gD were also found.

PubMed Disclaimer

References

    1. J Virol. 1983 Feb;45(2):634-47 - PubMed
    1. J Virol. 1979 Dec;32(3):779-89 - PubMed
    1. J Virol. 1980 Nov;36(2):429-39 - PubMed
    1. Virology. 1976 Aug;73(1):286-94 - PubMed
    1. J Virol. 1968 Jan;2(1):48-55 - PubMed

Publication types

Substances

LinkOut - more resources