Ohnuma H, Takahashi K, Kishimoto S, Machida A, Imai M, Mishiro S, Usuda S, Oda K, Nakamura T, Miyakawa Y
Gastroenterology. 1986 Mar;90(3):695-701. doi: 10.1016/0016-5085(86)91125-x.
Large hepatitis B surface antigen polypeptides with apparent molecular sizes of 39,000 and 43,000 daltons (P39 and P43) were liberated from a purified preparation of Dane particles of subtype adr. They were tested for reactivity with monoclonal antibodies raised against three synthetic oligopeptides representing fundamental sequences of the pre-S region in deoxyribonucleic acid of hepatitis B virus (subtype adr), as well as with monoclonal antibody against the major surface antigen polypeptide (P22) coded for by the S gene. Both P39 and its glycosylated form P43 bound to all four monoclonal antibodies, thereby indicating that they were coded for by the sequence of 1200 nucleotides, from the second ATG codon in the pre-S region to the stop codon of the S gene. Both P39 and P43 bound to polymerized human and chimpanzee albumins, but not to polymerized albumin from species without susceptibility to hepatitis B virus. Due to their presence in Dane particles and the expression of a polyalbumin receptor, the immune responses against P39 and P43 may have significance in infection with hepatitis B virus and its immunoprophylaxis.
从adr亚型的丹氏颗粒纯化制剂中释放出表观分子大小为39,000和43,000道尔顿的大型乙肝表面抗原多肽(P39和P43)。对它们进行了检测,以确定其与针对代表乙肝病毒(adr亚型)脱氧核糖核酸前S区基本序列的三种合成寡肽产生的单克隆抗体,以及与针对由S基因编码的主要表面抗原多肽(P22)的单克隆抗体的反应性。P39及其糖基化形式P43均与所有四种单克隆抗体结合,从而表明它们由前S区第二个ATG密码子至S基因终止密码子的1200个核苷酸序列编码。P39和P43均与聚合的人及黑猩猩白蛋白结合,但不与对乙肝病毒无易感性物种的聚合白蛋白结合。由于它们存在于丹氏颗粒中并表达多白蛋白受体,针对P39和P43的免疫反应可能在乙肝病毒感染及其免疫预防中具有重要意义。