Isaguliants M G, Kadoshnikov Iu P, Kalinina T I, Khuliakov Iu E, Semiletov Iu A, Smirnov V D, Wahren B
Swedish Institute for Infectious Disease Control, Stockholm, Sweden.
Biokhimiia. 1996 Mar;61(3):532-45.
Hybrids of the core protein of hepatitis B virus (HBcAg) have been designed which carry N-terminal insertions of B- and T-cell epitopes of HIV-1 an immunodominant B-epitope from gp41, a T-cell epitope from p34 pol, and a cluster of B- and T-cell epitopes from p17 gag. The hybrids have been synthesized using two expression systems-one based on the thermoinducible PR promoter of bacteriophage lambda and the other one based on phi 10 promoter of bacteriophage T7 with 3-5% and 7-14% yields, respectively. The hybrids have dual HBV and HIV-1 immunospecificity and are assembled into particles similar to those formed by the protein carrier HBcAg. Sandwich ELISA and immune electron microscopy revealed that HIV-1 epitopes are exposed on the surface of the particles.
已设计出乙型肝炎病毒核心蛋白(HBcAg)的杂交体,其携带HIV-1的B细胞和T细胞表位的N端插入序列,gp41的一个免疫显性B表位、p34 pol的一个T细胞表位以及p17 gag的一组B细胞和T细胞表位。使用两种表达系统合成了这些杂交体,一种基于噬菌体λ的热诱导PR启动子,另一种基于噬菌体T7的phi 10启动子,产率分别为3-5%和7-14%。这些杂交体具有双重的HBV和HIV-1免疫特异性,并组装成类似于由蛋白质载体HBcAg形成的颗粒。夹心ELISA和免疫电子显微镜显示,HIV-1表位暴露在颗粒表面。