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Journal of Virology, October 2001, p. 9201-9209, Vol. 75, No. 19
Forschungsschwerpunkt für Angewandte
Tumorvirologie, Deutsches Krebsforschungszentrum Heidelberg, 69120 Heidelberg,1 and Gesellschaft
für Biotechnologische Forschung, 38124 Braunschweig,2 Germany
Received 18 May 2001/Accepted 2 July 2001
Expression of the structural proteins L1 and L2 of the human
papillomaviruses (HPV) is tightly regulated. As a consequence, attempts
to express these prime-candidate genes for prophylactic vaccination
against papillomavirus-associated diseases in mammalian cells by means
of simple DNA transfections result in insufficient production of the
viral antigens. Similarly, in vivo DNA vaccination using HPV L1 or L2
expression constructs produces only weak immune responses. In this
study we demonstrate that transient expression of the HPV type 16 L1
and L2 proteins can be highly improved by changing the RNA coding
sequence, resulting in the accumulation of significant amounts of
virus-like particles in the nuclei of transfected cells. Data presented
indicate that, in the case of L1, adaptation for codon usage accounts
for the vast majority of the improvement in protein expression, whereas
translation-independent posttranscriptional events contribute only to a
minor degree. Finally, the adapted L1 genes demonstrate strongly
increased immunogenicity in vivo compared to that of unmodified L1 genes.
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.19.9201-9209.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Enhancement of Capsid Gene Expression: Preparing the Human
Papillomavirus Type 16 Major Structural Gene L1 for DNA
Vaccination Purposes
*
Corresponding author. Mailing address: DKFZ-ATV F0302,
Im Neuenheimer Feld 242, 69120 Heidelberg, Germany. Phone:
49-6221-424628. Fax: 49-6221-424902. E-mail:
Martin.Mueller{at}dkfz.de.
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