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[从人噬菌体展示文库中分离和鉴定抗β-淀粉样蛋白1-42可溶性寡聚体的人单链Fv抗体]

[Isolation and identification of a human single chain Fv antibody against amyloid-beta 1-42 soluble oligomers from a human phage display library].

作者信息

Bao Fuxiang, He Jinsheng, Cao Guifang, Yin Fan, Wang Xin, Pang Siyuan, Zhang Ying, Hong Tao

机构信息

College of Life Sciences & Bioengineering, Beijing Jiaotong University, Beijing 100044, China.

出版信息

Sheng Wu Gong Cheng Xue Bao. 2009 Aug;25(8):1195-203.

Abstract

To get specific scFv (Single-chain fragment variable) antibody against soluble Abeta1-42(Amyloid-beta) oligomers, we constructed a human single-chain Fv (scFv) antibody library by phage display technology. Using RT-PCR, we amplified the variable heavy (VH) and variable light (VL) genes from peripheral blood lymphocytes (PBL). Then we obtained the scFv fragments through SOE-PCR, and the scFv fragments were cloned into the vector pCANTAB5E and electroporated into competent Escherichia coli TG1 cells. Consequently, a scFv phage display library containing 2.5 x 10(9) clones was constructed. The recombinant phagemids were rescued by reinfection of helper phage M13K07. Recombinant phages specific for Abeta1-42 oligomers were enriched after four rounds of biopanning and the antigen-positive clones were selected from the enriched clones by phage ELISA. Positive clone B19 was used to infect E. coli HB2151 to express soluble scFv antibody. SDS-PAGE and Western blotting analysis showed that the soluble scFv B19 antibody was expressed successfully and could bind specifically to Abeta1-42 trimer and protofiber. The specific scFv against Abeta1-42 oligomers can be used in the therapeutic research on Alzheimer's disease.

摘要

为获得针对可溶性淀粉样β蛋白1-42(Aβ)寡聚体的特异性单链抗体可变区(scFv)抗体,我们利用噬菌体展示技术构建了一个人源单链抗体可变区(scFv)抗体文库。通过逆转录聚合酶链反应(RT-PCR),我们从外周血淋巴细胞(PBL)中扩增出重链可变区(VH)和轻链可变区(VL)基因。然后通过重叠延伸聚合酶链反应(SOE-PCR)获得scFv片段,并将这些scFv片段克隆到载体pCANTAB5E中,再电穿孔导入感受态大肠杆菌TG1细胞。最终,构建了一个包含2.5×10⁹个克隆的scFv噬菌体展示文库。通过辅助噬菌体M13K07的再次感染拯救重组噬菌粒。经过四轮生物淘选后,富集了针对Aβ1-42寡聚体的重组噬菌体,并通过噬菌体酶联免疫吸附测定(ELISA)从富集的克隆中筛选出抗原阳性克隆。阳性克隆B19用于感染大肠杆菌HB2151以表达可溶性scFv抗体。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和蛋白质免疫印迹分析表明,可溶性scFv B19抗体成功表达,并且能够特异性结合Aβ1-42三聚体和原纤维。针对Aβ1-42寡聚体的特异性scFv可用于阿尔茨海默病的治疗研究。

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