Heermann K H, Goldmann U, Schwartz W, Seyffarth T, Baumgarten H, Gerlich W H
J Virol. 1984 Nov;52(2):396-402. doi: 10.1128/JVI.52.2.396-402.1984.
The sequence of hepatitis B virus DNA contains an open reading frame which codes for a not-yet-identified protein of at least 389 amino acids. Only the products starting at the third (GP33/GP36) or the fourth (P24/GP27) initiation signal have been characterized as components of the viral surface antigen. We found a larger protein, P39, and its glycosylated form, GP42, in hepatitis B virus particles and viral surface antigen filaments. Immunological cross-reactions showed that P39/GP42 is partially homologous to P24/GP27 and GP33/GP36. The unique portion of its sequence bound monoclonal antibodies which had been induced by immunization with hepatitis B virus particles. Proteolytic cleavage patterns and subtype-specific size differences suggested that the sequence of P39 starts with the first initiation signal of the open reading frame. Its amino-terminal part (pre-s coded) is exposed at the viral surface and, probably, is highly immunogenic. A model is presented of how the open reading frame for the viral envelope leads to defined amounts of three different proteins.
乙肝病毒DNA序列包含一个开放阅读框,该阅读框编码一种尚未确定的至少含389个氨基酸的蛋白质。只有从第三个(GP33/GP36)或第四个(P24/GP27)起始信号开始产生的产物被鉴定为病毒表面抗原的成分。我们在乙肝病毒颗粒和病毒表面抗原丝中发现了一种更大的蛋白质P39及其糖基化形式GP42。免疫交叉反应表明,P39/GP42与P24/GP27和GP33/GP36部分同源。其序列的独特部分与用乙肝病毒颗粒免疫诱导产生的单克隆抗体结合。蛋白水解切割模式和亚型特异性大小差异表明,P39的序列始于开放阅读框的第一个起始信号。其氨基末端部分(前S编码区)暴露于病毒表面,可能具有高度免疫原性。本文提出了一个关于病毒包膜开放阅读框如何导致产生特定量的三种不同蛋白质的模型。