IDENTIFICATION OF POLYMERIZED-ALBUMIN RECEPTOR DOMAIN IN THE PRE-S2-REGION OF HEPATITIS-B VIRUS SURFACE ANTIGEN-M PROTEIN

被引:12
作者
ITOH, Y
KURODA, S
MIYAZAKI, T
OTAKA, S
FUJISAWA, Y
机构
[1] Biology Research Laboratories, Takeda Chemical Industries, Ltd., Yodogawa-ku, Osaka
关键词
HEPATITIS-B VIRUS SURFACE ANTIGEN; PRE-S2-REGION; POLYMERIZED-ALBUMIN RECEPTOR; VACCINE; GENE MODIFICATION; IMMUNE ELECTRON MICROSCOPY;
D O I
10.1016/0168-1656(92)90100-N
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 0836 [生物工程]; 090102 [作物遗传育种]; 100705 [微生物与生化药学];
摘要
The pre-S2-coding region in the hepatitis B virus surface antigen M (P31; pre-S2 + S) protein gene was modified to identify a polymerized-albumin receptor (PAR) domain by deleting restriction fragments or performing site-directed mutagenesis. The modified M protein genes (M-P31x; x = d, e, f, h and i) were cloned into the yeast generalized-expression vector pGLD 906-1 and expressed in Saccharomyces cerevisiae under the control of yeast glyceraldehyde-3-phosphate dehydrogenase gene promoter. The PAR activities of these gene products suggested that the PAR domain is located in the hydrophilic and highly conserved domain in the pre-S2 region (around Leu12 approximately Tyr21). Antibodies specific for a pre-S2 peptide (Phe8 approximately Pro34, subtype adr), which covers the PAR domain, were purified from sera of rabbits immunized with yeast-derived M protein particles having a natural PAR domain. Immune electron microscopy showed that the purified antibodies could aggregate HBV particles. Therefore, it was speculated that the PAR domain overlapped with the dominant virus-neutralizing and virus-protecting epitopes.
引用
收藏
页码:71 / 82
页数:12
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