Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, Vienna, Austria.
Institute of Hydrochemistry and Chair for Analytical Chemistry, Technical University Munich, Munich, Germany.
Plant Biotechnol J. 2018 Jan;16(1):27-38. doi: 10.1111/pbi.12746. Epub 2017 Jun 5.
Antibody MC10E7 is one of a small number of monoclonal antibodies that bind specifically to [Arg4]-microcystins, and it can be used to survey natural water sources and food samples for algal toxin contamination. However, the development of sensitive immunoassays in different test formats, particularly user-friendly tests for on-site analysis, requires a sensitive but also cost-effective antibody. The original version of MC10E7 was derived from a murine hybridoma, but we determined the sequence of the variable regions using the peptide mass-assisted cloning strategy and expressed a scFv (single-chain variable fragment) format of this antibody in yeast and a chimeric full-size version in leaves of Nicotiana tabacum and Nicotiana benthamiana to facilitate inexpensive and scalable production. The specific antigen-binding activity of the purified antibody was verified by surface plasmon resonance spectroscopy and ELISA, confirming the same binding specificity as its hybridoma-derived counterpart. The plant-derived antibody was used to design a lateral flow immunoassay (dipstick) for the sensitive detection of [Arg4]-microcystins at concentrations of 100-300 ng/L in freshwater samples collected at different sites. Plant-based production will likely reduce the cost of the antibody, currently the most expensive component of the dipstick immunoassay, and will allow the development of further antibody-based analytical devices and water purification adsorbents for the efficient removal of toxic contaminants.
抗体 MC10E7 是少数能特异性结合 [Arg4]-微囊藻毒素的单克隆抗体之一,可用于调查天然水源和食物样本中是否存在藻毒素污染。然而,要开发不同测试格式的灵敏免疫分析方法,特别是用于现场分析的用户友好型测试,就需要一种灵敏且具有成本效益的抗体。MC10E7 的原始版本源自鼠杂交瘤,但我们使用肽质量辅助克隆策略确定了可变区的序列,并在酵母中表达了该抗体的 scFv(单链可变片段)形式,在烟草和黄花烟的叶片中表达了嵌合全长形式,以促进廉价和可扩展的生产。通过表面等离子体共振光谱和 ELISA 验证了纯化抗体的特异性抗原结合活性,证实其与杂交瘤衍生的抗体具有相同的结合特异性。该植物来源的抗体被用于设计侧向流动免疫分析(试纸条),用于灵敏检测不同地点采集的淡水中浓度为 100-300ng/L 的 [Arg4]-微囊藻毒素。基于植物的生产可能会降低抗体的成本,目前这是试纸条免疫分析中最昂贵的组成部分,并将允许开发进一步基于抗体的分析设备和水净化吸附剂,以有效去除有毒污染物。