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作 者:韦秀梅[1] 绳秀珍[1] 唐小千[1] 邢婧[1] 战文斌[1]
机构地区:[1]中国海洋大学海水养殖教育部重点实验室,青岛266003
出 处:《海洋与湖沼》2010年第2期286-292,共7页Oceanologia Et Limnologia Sinica
基 金:国家重点基础研究发展计划"973";2006CB101806号;国家高技术研究发展计划"863";2006AA100312号
摘 要:以前期已制备的抗WSSV囊膜蛋白单克隆抗体4G9(Ab1)杂交瘤细胞生产小鼠腹水,腹水经辛酸-硫酸铵法、ProteinG亲和层析法纯化后,用以制备兔抗血清,所得血清经纯化得到粗提的兔抗WSSV独特型抗体(Ab2)。采用竞争酶联免疫吸附实验、间接免疫荧光法、斑点免疫印迹和蛋白免疫印迹等实验方法分析了Ab2特性,结果表明:Ab2能识别Ab1并与WSSV竞争Ab1的抗原结合位点,是具有模拟WSSV特性的抗独特型抗体;Ab2能与中国对虾血细胞结合,并能部分阻断WSSV与血细胞膜的结合;其与中国对虾血细胞膜上结合的蛋白分子量分别为94.5、51.5和27.0kDa,由此推断,这三个蛋白为WSSV在中国对虾血细胞膜上的结合蛋白。本研究结果可为进一步研究WSSV侵染机理提供资料。During the past more than ten years since a white spot syndrome virus (WSSV) disease outbreak in 1993, many research papers have been published on the pathogen, pathology, detection and diagnostic methods of the disease. Recent works focused mainly on the infection mechanism and searching the strategies of prophylaxis and control of WSSV infection. The purpose of this work was to produce rabbit anti-idiotypic antibody of WSSV (Ab2), analyze its characteriza- tion, and find a new way to study WSSV infection mechanism. Anti-WSSV envelope protein monoclonal antibody (Abl), which was produced previously, was purified from ascitic fluid using caprylic acid-ammonium sulfate (CA-AS) and Protein G agrose, then used to immunize rabbit, and finally Ab2 was purified from rabbit antiserum using CA-AS. The Ab2 was characterized by enzyme-linked immunosorbent assay (ELISA), indirect immunofluorescence assay (IIFA), Dot-blot and Western-blot. Results of competitive ELISA indicate that Ab2 could recognize Abl specifically and inhibit competitively the binding of WSSV with Ab1, implying that Ab2 could compete against the same paratope on Abl with WSSV, and represent an internal image of WSSV. In the meantime, IIFA proved that Ab2 could bind to the haemocyte membrane of Chinese shrimp (Fenneropenaeus chinensis). The results of both Dot-blot and ELISA blocking experiments show that Ab2 could block the binding of WSSV to haemocyte membrane. By Western-blot, three protein bands of 94.5, 51.5 and 27.0kDa were recognized specifically by Ab2, and they were considered to be WSSV binding protein on Chinese shrimp haemocyte membrane.
关 键 词:独特型抗体 对虾白斑症病毒 竞争酶联免疫吸附实验 DOT-BLOT 间接免疫荧光法 WESTERN-BLOT
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