摘要
采用我室建立的短肽点免疫结合试验确定Pre-S_(2)蛋白B细胞表位的精细特异性。结果发现Pre-S_(2)蛋白的B细胞识别部位(14~24)可进一步区分为两个部分交叠的表位:14~21和18~24,从而绘出了Pre-S_(2)蛋白B细胞表位图谱。这对设计新一代疫苗及诊断试剂有指导意义。
The new dot immunobinding assay for small peptides established
in our laboratory was employed in thestudy of the fine specificity of the dominant antibody
binding site in Pre-S_(2)region of HBV surface antign. Two over-lapping epitopes.14~21 and
18~ 24,were identified within the dominant antibody binding site(14~24),and six aminoacid
residues, ̄(14)D, ̄(15)P, ̄(20)L, ̄(21) Y, ̄(18)R, ̄(24)A,were proved impertant for those two
epitopes, These findings are instructive formolecular design of the new generation HBV
vaccines and diagncotic agents.
出处
《免疫学杂志》
CAS
CSCD
北大核心
1994年第2期80-82,共3页
Immunological Journal
基金
国家自然科学基金及
全军"八五"青年基金
关键词
Pre-S(2)
蛋白
表位
合成肽
B细胞
Pre-S_(2) region of HBsAg,Epitope. Dot
immunobinding assay.Peptide