首页> 外文期刊>Academic Journal of Xi'an Jiaotong University >THE CONSTRUCTION AND EXPRESSION OF THE MURINE SCFV GENE IN E. COLI AGAINST HUMAN CERVICAL CANCER
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THE CONSTRUCTION AND EXPRESSION OF THE MURINE SCFV GENE IN E. COLI AGAINST HUMAN CERVICAL CANCER

机译:鼠SCFV基因在大肠杆菌中的表达及其在人宫颈癌中的表达。

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Objective To obtain the gene of murine Single chain Fv fragment (ScFv) against human cervical cancer and to express it in E. coli . Methods The variable region gene fragments of the heavy and light chains, which were amplified respectively using recombinant DNA techniques from CsA125 hyhridoma cells, were spliced together through a flexible linker to ScFv against human cervical cancer. The ScFv genes were then cloned into expression vector pCANTAB 5E and expressed in E. coli HB2151 and TG1 respectively. The soluble ScFv were characterized by SDS-PAGE and Western blot. The antigen-binding activities of the soluble and phage displayed ScFv were assayed by ELISA and cell immunohistochemical analysis. Results The expressed ScFv antibodies were soluble and phage displayed. The soluble ScFv secreted and expressed in E. coli HB2151 induced by IPTG were confirmed with SDS-PAGE, Western blot and ELISA. The specific binding capacity of the soluble and phage displayed ScFv to the surface associated antigen of human cervical cancer cell line was further confirmed with immunohistochemical studies. Conclusion The soluble and phage displayed ScFv expressed in E. coli against human cervical cancer showed high, specific affinity for the cervical cancer cell line surface associated antigen.
机译:目的获得抗人宫颈癌的鼠单链Fv片段基因(ScFv)并在大肠杆菌中表达。方法通过重组DNA技术分别从CsA125透明膜瘤细胞中扩增出重链和轻链可变区基因片段,并通过柔性接头与抗人宫颈癌的ScFv连接在一起。然后将ScFv基因克隆到表达载体pCANTAB 5E中,并分别在大肠杆菌HB2151和TG1中表达。通过SDS-PAGE和蛋白质印迹对可溶性ScFv进行表征。通过ELISA和细胞免疫组织化学分析测定可溶性和噬菌体展示的ScFv的抗原结合活性。结果表达的ScFv抗体可溶并显示噬菌体。用SDS-PAGE,Western blot和ELISA证实IPTG诱导的在大肠杆菌HB2151中分泌和表达的可溶性ScFv。通过免疫组织化学研究进一步证实了可溶性和噬菌体展示的ScFv与人宫颈癌细胞系表面相关抗原的特异性结合能力。结论在大肠杆菌中表达的抗人宫颈癌的可溶性和噬菌体展示的ScFv对宫颈癌细胞株表面相关抗原具有很高的特异性亲和力。

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