Tan Geok Hun, Yusoff Khatijah, Seow Heng Fong, Tan Wen Siang
Department of Microbiology, Faculty of Biotechnology and Biomolecular Sciences, Universiti Putra Malaysia, Serdang, Selangor, Malaysia.
J Med Virol. 2005 Dec;77(4):475-80. doi: 10.1002/jmv.20479.
The immunodominant region of hepatitis B virus (HBV) located in the viral small surface antigen (S-HBsAg) elicits virus-neutralizing and protective antibodies. In order to develop an easy and inexpensive method to produce this region without the need for extensive purification, amino acid residues 111-156 of S-HBsAg were fused to the C-terminal end of the 10B capsid protein of T7 phage. Western blotting and ELISA confirmed the expression of the recombinant protein on the surface of the phage particles. The recombinant phage exhibited the antigenic and immunogenic characteristics of HBsAg, illustrating its potential as an immunological reagent and vaccine.
位于乙肝病毒(HBV)病毒小表面抗原(S-HBsAg)中的免疫显性区域可引发病毒中和抗体和保护性抗体。为了开发一种无需大量纯化即可生产该区域的简便且低成本的方法,将S-HBsAg的111-156位氨基酸残基与T7噬菌体的10B衣壳蛋白的C末端融合。蛋白质免疫印迹法和酶联免疫吸附测定法证实了重组蛋白在噬菌体颗粒表面的表达。重组噬菌体展现出HBsAg的抗原性和免疫原性特征,表明其作为免疫试剂和疫苗的潜力。