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Selection of Diethylstilbestrol-Specific Single-Chain Antibodies from a Non-Immunized Mouse Ribosome Display Library

机译:从非免疫小鼠核糖体展示文库中选择己烯雌酚特异的单链抗体

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摘要

Single chain variable fragments (scFvs) against diethylstilbestrol (DES) were selected from the splenocytes of non-immunized mice by ribosome display technology. A naive library was constructed and engineered to allow in vitro transcription and translation using an E. coli lysate system. Alternating selection in solution and immobilization in microtiter wells was used to pan mRNA-ribosome-antibody (ARM) complexes. After seven rounds of ribosome display, the expression vector pTIG-TRX containing the selected specific scFv DNAs were transformed into Escherichia coli BL21 (DE3) for expression. Twenty-six positive clones were screened and five clones had high antibody affinity and specificity to DES as evidenced by indirect competitive ELISA. Sequence analysis showed that these five DES-specific scFvs had different amino acid sequences, but the CDRs were highly similar. Surface plasmon resonance (SPR) analysis was used to determine binding kinetics of one clone (30-1). The measured KD was 3.79 µM. These results indicate that ribosome display technology can be used to efficiently isolate hapten-specific antibody (Ab) fragments from a naive library; this study provides a methodological framework for the development of novel immunoassays for multiple environmental pollutants with low molecular weight detection using recombinant antibodies.
机译:通过核糖体展示技术从未免疫小鼠的脾细胞中选择了针对己烯雌酚(DES)的单链可变片段(scFvs)。构建并设计了幼稚的文库,以允许使用大肠杆菌裂解液系统进行体外转录和翻译。在溶液中交替选择并在微量滴定孔中固定用于淘选mRNA-核糖体-抗体(ARM)复合物。展示了七轮核糖体后,将含有选择的特定scFv DNA的表达载体pTIG-TRX转化到大肠杆菌BL21(DE3)中进行表达。如间接竞争ELISA所证实,筛选了26个阳性克隆,并且五个克隆对DES具有高抗体亲和力和特异性。序列分析表明这五个DES特异的scFv具有不同的氨基酸序列,但CDR高度相似。表面等离子体共振(SPR)分析用于确定一个克隆(30-1)的结合动力学。测得的KD为3.79 µM。这些结果表明,核糖体展示技术可用于从幼稚文库中有效分离半抗原特异性抗体(Ab)片段。该研究为使用重组抗体的低分子量检测开发多种环境污染物的新型免疫测定方法提供了方法学框架。

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