冯凡,许杨,王丹,雷达,孙澄浩.抗黄曲霉毒素B1独特型纳米抗体的表达及复性[J].食品安全质量检测学报,2013,4(4):1222-1227 |
抗黄曲霉毒素B1独特型纳米抗体的表达及复性 |
Prokaryotic expression and renaturation of anti-idiotype nanobody against aflatoxin B1 |
投稿时间:2013-07-16 修订日期:2013-08-18 |
DOI: |
中文关键词: 黄曲霉毒素B1 独特型抗体 纳米抗体 原核表达 复性 |
英文关键词:aflatoxin B1 anti-idiotype antibody nanobody prokaryotic expression renaturation |
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中文摘要: |
目的 快速制备大量具有生物活性的独特型纳米抗体F7。方法 构建pET22b-F7原核表达载体, 转化至大肠杆菌E. coli BL21(DE3)中进行诱导表达, 对诱导温度、诱导剂浓度和诱导时间进行优化。结果 独特型纳米抗体F7表达量有所增加但主要以包涵体形式存在。经过包涵体的溶解、复性获得了具有生物活性的抗AFB1独特型纳米抗体, ELISA证实复性后的蛋白依然存在对鼠源AFB1抗体的结合特性。结论 为后续抗体的性质研究和改造奠定了基础。 |
英文摘要: |
Objective To rapidly produce a large amount of anti-idiotype nanobody against aflatoxin B1 (AFB1). Methods Prokaryotic expression vector pET22b-F7 were constructed, and then transformed into E.coli BL21(DE3) for expression of anti-idiotype nanobody against aflatoxin B1 (AFB1). The conditions such as temperature, concentration of inducer, and induction time were optimized. Results The expression quantity of anti-idiotype nanobody F7 increased, with the main form of inclusion body. Anti-idiotype nanobody against AFB1 with bioactivity were obtained after dissolution and renaturation. ELISA results indicated that the renatured protein had the properties of combination with AFB1 antibody. Conclusion It provides a reference for further study of properties and subsequent transformation. |
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