大肠杆菌
降级(电信)
包涵体
包裹体(矿物)
化学
微生物学
生物
生物化学
计算机科学
基因
电信
矿物学
作者
А. С. Комолов,E. S. Bobrov,Е. П. Санникова,I. I. Gubaidullin,Н. О. Черноморова,Д. Г. Козлов
标识
DOI:10.1134/s0003683824700236
摘要
The production of target proteins in Escherichia coli cells can be greatly simplified if they are synthesized in a biologically active state as part of active inclusion bodies (AIBs), which can easily be isolated from cells by centrifugation. This is a new technology, so the question about the protective properties of AIBs specific for standard inclusion bodies still remains open. This work describes the synthesis of the recombinant protein L6KD-SUMO-[R34-GLP-1(7–37)], which forms AIB, in E. coli BL21(DE3) cells. This protein engineered from a novel, recently developed L6KD-SUMO platform incorporates a modified human glucagon-like peptide-1, R34-GLP-1(7–37), the active substance of Liraglutide-based drugs. It was shown that, the soluble protein His10-SUMO-[R34-GLP-1(7–37)] expressed by E. coli, retained the peptide intact only for 24 h, but the peptide integrity in the AIB composition was maintained over 70 h of cell cultivation. Thus, it is logical to assume that AIB formation has a protective effect on target compounds synthesized by the cell.
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