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作 者:杜进[1] 陈磊[1] 仲从浩 程超[1] 祝先潮 李荣秀[1]
机构地区:[1]微生物代谢国家重点实验室,生命科学技术学院上海交通大学,上海2002400
出 处:《安徽师范大学学报(自然科学版)》2014年第6期569-574,580,共7页Journal of Anhui Normal University(Natural Science)
基 金:国家科技重大专项(重大新药创制专项)资助(2014ZX09101043)
摘 要:为预测并鉴定人凝血因子IX(FIX)的线性B细胞表位.通过IEDB数据库及Discovery Studio软件预测FIX的B表位和白喉毒素T结构域(DTT)的B表位,用所预测的FIX的B表位替换某预测的DTT的B表位形成DTT-表位融合蛋白.通过基因工程技术制备各重组蛋白,并免疫小鼠,通过ELISA和Western-blot检测抗血清效价和特异性,通过等温量热滴定技术(ITC)测定抗体的亲和力.预测到4个FIX的B表位.用重组蛋白FIX-2-DTT免疫的小鼠产生了识别完整FIX的抗体,该抗体具有良好的特异性,其结合常数KD为106 M-1.表明FIX-2(306 NAAINKY312)是FIX的B表位,用重组蛋白FIX-2-DTT免疫小鼠能够产生特异性识别FIX且亲和力温和的抗体.In order to predict and identify linear B cell epitopes of human coagulation factor IX(FIX),the linear B cell epitopes of FIX and diphtheria toxin transmembrane domains structure(DTT)were predicted by IEDB database and Discovery Studio solftware.According to the principle of"similar N-C distance",the predicted B cell epitopes of DTT were replaced by the predicted B cell epitopes of FIX in oder to form DTT-epitope fusion proteins.Fusion proteins were prepared by genetic engineering technology and subsequently used for immunization of Bal b/c mice.The titer and specificity of antiserum was measured by ELISA and Western-blot.The affinity of antibody was determined by isothermal titration calorimetry techniques(ITC).Results showed:Four B cell epitopes of FIX were predicted.The antibody that can recognize the complete FIX was produced in mice immunized with the FIX-2-DTT fusion protein,which has good specificity.The binding constant KD of the antibody is 106 M-1.FIX-2(306 NAAINKY312)is a B epitope of FIX.The anti-FIX antibody with good specificity and gentle affinity could be produced by immunizing mice with FIX-2-DTT fusion protein.
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