Li Jingquan, Xu Yongping, Wang Xitao, Li Yuan, Wang Lili, Li Xiaoyu
School of Life Science and Biotechnology, Dalian University of Technology, Dalian 116024, China.
School of Life Science and Biotechnology, Dalian University of Technology, Dalian 116024, China; Ministry of Education Center for Food Safety of Animal Origin, Dalian 116620, China.
Int Immunopharmacol. 2016 Jun;35:149-154. doi: 10.1016/j.intimp.2016.02.024. Epub 2016 Apr 16.
The purpose of this study was to construct a single-chain variable fragment (scFv) antibody from chicken egg yolk immunoglobulin (IgY) by means of genetic engineering and subsequent panning for a specific antibody against Staphylococcus aureus.
We amplified the scFv using blood and spleen obtained from 100-day-old Roman chickens immunized with inactivated S. aureus and subsequently constructed a T7 phage display antibody library using phage display technology. Four non-repeated blood scFv and 6 spleen scFv were obtained following 3 rounds of panning of the T7 phage display antibody library, enzyme-linked immunosorbent assay and sequencing. These 10 scFv were cloned into the prokaryotic expression vector pCold I with expression induced at a low temperature. Four soluble proteins were obtained. Among them, soluble protein SFV6 derived from the spleen showed good reactivity against S. aureus using indirect ELISA and produced a particularly strong antibacterial effect in vitro.
We were successful in isolating a highly specific scFv antibody against S. aureus from the spleen phage display library. This study provides a simple and rapid method for the quick preparation of a large number of antibodies against S. aureus and provides the foundation for the positioning of antibodies in the organism and the study of the antibacterial mechanism through which the antibody functions.
本研究的目的是通过基因工程手段从鸡卵黄免疫球蛋白(IgY)构建单链可变片段(scFv)抗体,随后淘选针对金黄色葡萄球菌的特异性抗体。
我们使用从用灭活金黄色葡萄球菌免疫的100日龄罗曼鸡获得的血液和脾脏扩增scFv,随后利用噬菌体展示技术构建T7噬菌体展示抗体文库。在对T7噬菌体展示抗体文库进行三轮淘选、酶联免疫吸附测定和测序后,获得了4个非重复的血液scFv和6个脾脏scFv。将这10个scFv克隆到原核表达载体pCold I中,并在低温下诱导表达。获得了4种可溶性蛋白。其中,源自脾脏的可溶性蛋白SFV6使用间接ELISA对金黄色葡萄球菌显示出良好的反应性,并在体外产生了特别强的抗菌作用。
我们成功地从脾脏噬菌体展示文库中分离出一种针对金黄色葡萄球菌的高度特异性scFv抗体。本研究提供了一种简单快速的方法,用于快速制备大量针对金黄色葡萄球菌的抗体,并为抗体在生物体中的定位以及抗体发挥作用的抗菌机制研究奠定了基础。