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Journal of Virology, March 1999, p. 2153-2160, Vol. 73, No. 3
Department of Medical Microbiology,
University of Göttingen, D-37075 Göttingen, Germany
Received 27 July 1998/Accepted 20 November 1998
We generated a large number of mutations in the hepatitis B virus
(HBV) core gene inserted into a bacterial expression vector. The new
mutagenesis procedure generated deletions and insertions (as sequence
repeats) of various lengths at random positions between M1 and E145 but
not substitutions. The R-rich 30-amino-acid C-terminal domain was not
analyzed. A total of 50,000 colonies were tested with a polyclonal
human serum for the expression of hepatitis B core or e antigen. A
total of 110 mutants randomly chosen from 1,500 positive colonies were
genotyped. Deletions and insertions were clustered in four regions: D2
to E14, corresponding to the N-terminal loop in a model for the core
protein fold (B. Bottcher, S. A. Wynne, and R. A. Crowther,
Nature 386:88-91, 1997); V27 to P50 (second loop); L60 to V86 (upper
half of the alpha helix forming the N-terminal part of the spike and
the tip of the spike); and V124 to L140 (C-terminal part of the
C-terminal helix and downstream loop). Deletions or insertions in the
remaining parts of the molecule forming the compact center of the fold
seemed to destabilize the protein. Of the 110 mutations, 38 allowed
capsid formation in Escherichia coli. They mapped
exclusively to nonhelical regions of the proposed fold. The mutations
form a basis for subsequent analysis of further functions of the HBV
core protein in the viral life cycle.
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Extensive Mutagenesis of the Hepatitis B Virus Core
Gene and Mapping of Mutations That Allow Capsid Formation
*
Corresponding author. Mailing address: Department of
Medical Microbiology, University of Göttingen, Kreuzbergring 57, D-37075 Göttingen, Germany. Phone: 49 551 39 5759. Fax: 49 551 39 5860. E-mail: VBRUSS{at}GWDG.DE.
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