中国仓鼠卵巢细胞
大肠杆菌
克隆(编程)
免疫球蛋白轻链
细胞质
生物
蛋白质工程
二硫键
高分子
生物化学
分子生物学
化学
抗体
计算生物学
基因
细胞培养
遗传学
酶
计算机科学
程序设计语言
作者
J.B. Eaglesham,Augusto F. García,Mehmet Berkmen
标识
DOI:10.1016/bs.mie.2021.06.040
摘要
Antibodies are globally important macromolecules, used for research, diagnostics, and as therapeutics. The common mammalian antibody immunoglobulin G (IgG) is a complex glycosylated macromolecule, composed of two heavy chains and two light chains held together by multiple disulfide bonds. For this reason, IgG and related antibody fragments are usually produced through secretion from mammalian cell lines, such as Chinese Hamster Ovary cells. However, there is growing interest in production of antibodies in prokaryotic systems due to the potential for rapid and cheap production in a highly genetically manipulable system. Research on oxidative protein folding in prokaryotes has enabled engineering of Escherichia coli strains capable of producing IgG and other disulfide bonded proteins in the cytoplasm, known as SHuffle. In this protocol, we provide a review of research on prokaryotic antibody production, guidelines on cloning of antibody expression constructs, conditions for an initial expression and purification experiment, and parameters which may be optimized for increased purification yields. Last, we discuss the limitations of prokaryotic antibody production, and highlight potential future avenues for research on antibody expression and folding.
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