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作 者:武国军[1] 王栋[1] 王禾[1] 袁建林[1] 于磊[1] 张更[1] 郝晓柯[2] 白玉杰[3] 王智[3]
机构地区:[1]第四军医大学西京医院泌尿外科,西安710033 [2]第四军医大学西京医院检验科,西安710033 [3]第四军医大学基础部生物化学与分子生物学教研室
出 处:《中华实验外科杂志》2006年第5期585-587,共3页Chinese Journal of Experimental Surgery
基 金:国家自然科学基金资助项目(39900180);全军重点实验室研究基金资助项目(1997-71-22)
摘 要:目的探讨人p53四聚功能域在提高抗前列腺特异抗原(PSA)/抗人CD3双特异性单链抗体(scFv)亲和力方面的作用。方法利用递归聚合酶链反应(PCR)法扩增人IgG3上游铰链区与人p53四聚功能域融合基因,克隆入pUC19载体中构建pUC19/IgG3/p53克隆载体。将抗 PSA/CD3双特异性scFv克隆入pUC19/IgG3/p53载体中,构建多价抗PSA/CD3双特异性scFv融合基因。将融合基因克隆入真核表达载体pSeeTag2-B中,转染HeLa细胞进行表达,表达产物纯化后利用流式细胞仪进行活性测定。结果获得了多价抗PSA/CD3双特异性scFv融合基因,基因全长1638 bp,可编码546个氨基酸,与已发表的抗PSA/CD3双特异性scFv和人p53四聚功能域基因cDNA序列一致。表达产物经SDS-PAGE和Western印迹实验证实为约67×103的特异蛋白条带,纯化后经流式细胞仪检测可以特异性地结合PC-3细胞和人外周血单个核细胞(PBMC),亲和力高于双特异性scFv。结论人IgG3上游铰链区/p53四聚功能域基因与抗PSA/CD3双特异性 scFv基因融合后表达产物的功能性亲和力大大提高,为提高抗体的功能性亲和力开辟了新的思路。Objective To fuse the genes of p53 tetramerization domain and bispecific single chain Fv antibody gene specific for human prostate specific antigen (PSA) and CD3 molecule [ scFv2 (PSA/ CD3) ], and exploit a new way to improve the functional affinity of antibody. Methods The human IgG3 upper hinge/human p53 tetramerization domain fusion gene was obtained by recursive polymerase chain reaction (PCR), and was inserted into pUC19 to construct cloning plasmid pUC19/IgG3/p53. The scFv2 (PSA/CD3) was cloned into pUC19/IgG3/p53 to construct multivalent scFv2 (PSA/CD3) which was then subeloned into the pSecTag2-B expression plasmid. Then the pSecTag2-B plasmids containing the fusion gene were transfected into HeLa cells. The expression products were analyzed by both SDS-PAGE and Western blot, then were purified with Ni^2+ -NTA superflow affinity chromatography. The binding affinity for PC-3 cells and peripheral blood mononuclear cells (PBMCs) was measured by flow cytometry. Results The multivalent scFv2 (PSA/CD3) gene consisted of 1 638 bp encoding 546 amino acid residues, and was the same as that reported before. The expression products of the multivalent scFv2 (PSA/CD3) were confirmed by SDS-PAGE and Western blot. After purified with Ni^2+ -NTA superflow affinity chromatography, the multivalent scFv2 (PSA/CD3) showed significantly stronger binding to PC- 3 cells and PBMCs than scFv2 (PSA/CD3). Conclusion The multivalent scFv2 (PSA/CD3) exhibits much higher functional affinity than scFv2 (PSA/CD3), which may break a new path to the improvement of functional affinity of antibody.
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