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作 者:张璐[1] 王延群[2] 郝立沙 高明明[2] 李爱东[2] 陶冶[2] 李莉[2] 涂亚斌[2] 蔡雪辉[2] 路义鑫[1]
机构地区:[1]东北农业大学动物医学学院,黑龙江哈尔滨150030 [2]中国农业科学院哈尔滨兽医研究所兽医生物技术国家重点实验室/动物疫病诊断中心,黑龙江哈尔滨150001
出 处:《中国预防兽医学报》2014年第4期310-313,共4页Chinese Journal of Preventive Veterinary Medicine
基 金:"十二五"高技术研究发展计划(2011AA10A213);哈尔滨市科技攻关计划项目(2010AA6AN083);黑龙江省自然科学基金(C201047)
摘 要:为制备猪圆环病毒2型(PCV2)Cap蛋白单克隆抗体(MAb)及鉴定其抗原表位,本研究采用PCV2去核定位信号Cap蛋白(dCap),通过杂交瘤技术制备1株杂交瘤细胞株(4E2),制备小鼠腹水效价达1∶64 000,亚类鉴定为IgG1/κ链。Western blot分析显示,该株MAb与毕赤酵母表达的dCap和原核表达的Cap蛋白均可以发生特异性免疫反应。采用肽扫描法对MAb的非核定位信号区进行抗原表位鉴定,结果表明该MAb可以识别的线性表位区域为131TKATALTYDPYVNYSS146。本实验结果为进一步研究Cap蛋白的结构和PCV2临床检测方法的建立奠定基础。To prepare monoclonal antibodies (MAb) against Cap protein of porcine circovirus Ⅱ (PCV2) and identify the antigen epitope, a MAb against PCV2 was prepared by lymphocyte hybridoma technique with the recombinant Cap protein without nuclear location signal (dCap) expressed by P.pastoria. The MAb was belonged to IgG1 subclass and κ light chain. The ELISA titer of MAb was 1:64 000 in ascites. Western blot indicated that MAb was reacted with PCV2-dCap expressed in P.pastoria and PCV2-Cap expressed in E.coli. IFA assay showed the MAb was reacted with PCV2 in PK15 cells. Furthermore, the MAb recognized dCap protein epitope of ^131TKATALTYDPYVNYSS^146 mapped by a serious of prokaryotic expressed peptides. The MAb prepared in this study is useful tool for developing immunological diagnostic techniques of PCV2 and further investigation of the Cap protein.
分 类 号:S852.65[农业科学—基础兽医学]
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