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Preparation of a Single-Chain Variable Fragment and a Recombinant Antigen-Binding Fragment against the Anti-Malarial Drugs, Artemisinin and Artesunate, and Their Application in an ELISA

机译:抗疟疾药物青蒿素和青蒿琥酯的单链可变片段和重组抗原结合片段的制备及其在ELISA中的应用

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摘要

Two different recombinant antibodies, a single-chain variable fragment (scFv) and an antigen-binding fragment (Fab), were prepared against artemisinin (AM) and artesunate (AS) and were developed for use in an enzyme-linked immunosorbent assay (ELISA). The recombinant antibodies, which were derived from a single monoclonal antibody against AM and AS (mAb 1C1) prepared by us, were expressed by Escherichia coli cells and their reactivity and specificity were characterized. As a result, to obtain sufficient signal in indirect ELISA, a much greater amount of a first antibody was needed in the use of scFv due to the differences of the secondary antibody and conformational stability. Therefore, we focused on the development of the recombinant Fab antibodies and applied it to indirect competitive ELISA. The specificity of the Fab was similar to that of mAb 1C1 in that it showed specific reactivity toward AM and AS only. The sensitivity of the icELISA (0.16 (mu)g/mL to 40 (mu)g/mL for AM and 8.0 ng/mL to 60 ng/mL for AS) was sufficient for analysis of antimalarial drugs, and its utility for quality control of analysis of Artemisia spp. was validated. The Fab expression and refolding systems provided a good yield of high-quality antibodies. The recombinant antibody against AM and AS provides an essential component of an economically attractive immunoassay and will be useful in other immunochemical applications for the analysis and purification of antimalarial drugs.
机译:针对青蒿素(AM)和青蒿琥酯(AS)制备了两种不同的重组抗体,即单链可变片段(scFv)和抗原结合片段(Fab),并开发用于酶联免疫吸附测定(ELISA) )。重组抗体是由我们制备的抗AM和AS的单克隆抗体(mAb 1C1)衍生的,并在大肠杆菌细胞中表达,并对其反应性和特异性进行了表征。结果,为了在间接ELISA中获得足够的信号,由于二抗和构象稳定性的差异,在使用scFv时需要大量的一抗。因此,我们专注于重组Fab抗体的开发,并将其应用于间接竞争ELISA。 Fab的特异性与mAb 1C1相似,因为它仅显示对AM和AS的特异性反应性。 icELISA的灵敏度(对于AM为0.16μg/ mL至40μμg/ mL,对于AS为8.0 ng / mL至60 ng / mL)足以用于分析抗疟药,并且其可用于质量控制蒿分析。被验证。 Fab表达和重折叠系统提供了高产率的高质量抗体。抗AM和AS的重组抗体提供了经济上有吸引力的免疫测定的重要组成部分,并将在其他免疫化学应用中用于抗疟药物的分析和纯化。

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