Literature DB >> 7683161

High level expression and phosphorylation of hepatitis B virus polymerase in insect cells with recombinant baculoviruses.

B Ayola1, P Kanda, R E Lanford.   

Abstract

The hepatitis B virus polymerase open reading frame, as well as various subdomains of polymerase, was expressed in insect cells using the recombinant baculovirus expression system. Full-length polymerase was expressed at very low levels in a Spodoptera frugiperda cell line, the amino-terminal domain of polymerase was expressed at high levels, and other constructs were expressed at intermediate levels. Infections of a Trichoplusia ni cell line with the same recombinant baculoviruses resulted in high levels of protein production for all polymerase constructs. Each of the polymerase polypeptides was phosphorylated in insect cells. Since polypeptides with non-overlapping sequences were phosphorylated, polymerase must be phosphorylated at a minimum of two sites.

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Year:  1993        PMID: 7683161     DOI: 10.1006/viro.1993.1270

Source DB:  PubMed          Journal:  Virology        ISSN: 0042-6822            Impact factor:   3.616


  9 in total

1.  Mapping of the hepatitis B virus reverse transcriptase TP and RT domains by transcomplementation for nucleotide priming and by protein-protein interaction.

Authors:  R E Lanford; Y H Kim; H Lee; L Notvall; B Beames
Journal:  J Virol       Date:  1999-03       Impact factor: 5.103

2.  Large-scale production and structural and biophysical characterizations of the human hepatitis B virus polymerase.

Authors:  Judit Vörös; Annika Urbanek; Gilles Jean Philippe Rautureau; Maggie O'Connor; Henry C Fisher; Alison E Ashcroft; Neil Ferguson
Journal:  J Virol       Date:  2013-12-18       Impact factor: 5.103

3.  A single amino acid in the reverse transcriptase domain of hepatitis B virus affects virus replication efficiency.

Authors:  X Lin; Z H Yuan; L Wu; J P Ding; Y M Wen
Journal:  J Virol       Date:  2001-12       Impact factor: 5.103

4.  Mapping of Functional Subdomains in the Terminal Protein Domain of Hepatitis B Virus Polymerase.

Authors:  Daniel N Clark; John M Flanagan; Jianming Hu
Journal:  J Virol       Date:  2017-01-18       Impact factor: 5.103

5.  Hepadnavirus reverse transcription initiates within the stem-loop of the RNA packaging signal and employs a novel strand transfer.

Authors:  J E Tavis; S Perri; D Ganem
Journal:  J Virol       Date:  1994-06       Impact factor: 5.103

6.  Transcomplementation of nucleotide priming and reverse transcription between independently expressed TP and RT domains of the hepatitis B virus reverse transcriptase.

Authors:  R E Lanford; L Notvall; H Lee; B Beames
Journal:  J Virol       Date:  1997-04       Impact factor: 5.103

7.  Nucleotide priming and reverse transcriptase activity of hepatitis B virus polymerase expressed in insect cells.

Authors:  R E Lanford; L Notvall; B Beames
Journal:  J Virol       Date:  1995-07       Impact factor: 5.103

8.  Evidence that the RNAseH activity of the duck hepatitis B virus is unable to act on exogenous substrates.

Authors:  Y Gong; E Yao; J E Tavis
Journal:  BMC Microbiol       Date:  2001-07-19       Impact factor: 3.605

Review 9.  Molecular, Evolutionary, and Structural Analysis of the Terminal Protein Domain of Hepatitis B Virus Polymerase, a Potential Drug Target.

Authors:  Timothy S Buhlig; Anastasia F Bowersox; Daniel L Braun; Desiree N Owsley; Kortney D James; Alfredo J Aranda; Connor D Kendrick; Nicole A Skalka; Daniel N Clark
Journal:  Viruses       Date:  2020-05-22       Impact factor: 5.048

  9 in total

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