摘要
用蔗糖密度梯度离心法纯化PHSA受体阳性的正常人肝细胞膜(HPM),通过Westernblot技术发现抗HBVPreS2(120~145)合成肽多克隆抗体可识别到两种抗原成份(70kD和120kD)。用蛋白酶K、脂肪酶、神经氨酸酶消化HPM后再进行Westernblot识别,结果表明这两种抗原成份分别具有糖脂蛋白和糖蛋白的性质。由于已知抗PreS2(120~145)是针对HBVPHSA受体抗原表位的抗体,故作者认为HPM上这两种不同性质的HBVPHSA受体相关抗原可能与肝细胞的PHSA受体密切相关,乙肝病毒PHSA受体与正常人肝细胞PHSA受体之间可能存在一定程度的结构相似性。
e purified the normal
human hepatocyte plasma membrane (HPM ) with sucrose gradient centrifugationsThe
hepatocytes had been previously tested as PHSA receptor positive. We found the polyclonal
antibody againstPres2(120~145)synthetic peptide,which was identified against HBV PHSA
receptor antigen epitopes,recog-nized two antigens of the normal human HPM with Western
blot. Molecular weight of the recognized antigens was70kD and 120kD respectively. As a
control, the SP2/0 cells which didn′t express PHSA receptor was not recog-nized by the
anti-PreS2 ( 120~145).Further experiment results suggested a glycoprotein nature for the
120kDantigen and a glycolipidprotein nature for the other one. We suggest that these two
antigens possessing a distinctchemical nature most relate to the PHSA receptor on normal
human HPM which also expressed two classes ofbinding site.Our studies would be useful to
further characterize the PHSA receptor of human hepatocytes.It wasalso important to realize the
immunopathogenesis of HBV and modify the hepatitis B vaccine.
出处
《中华微生物学和免疫学杂志》
CAS
CSCD
北大核心
1994年第4期249-252,共4页
Chinese Journal of Microbiology and Immunology
基金
国家自然科学基金
关键词
肝细胞膜
PHSA
受体
乙型肝炎病毒
PHSA
Anti-HBV
PreS2(120~145)
Normal human HPM
Western blot