中国仓鼠卵巢细胞
生物
生物制药
小RNA
细胞生物学
HEK 293细胞
计算生物学
细胞培养
重组DNA
细胞生长
细胞周期
细胞
遗传学
基因
作者
Masoume Bazaz,Ahmad Abdolzadeh,Morteza Azizi,Milad Soleimani,Fereidoun Mahboudi,Noushin Davoudi
标识
DOI:10.1007/s10529-022-03250-1
摘要
It is widely accepted that the growing demand for recombinant therapeutic proteins has led to the expansion of the biopharmaceutical industry and the development of strategies to increase recombinant protein production in mammalian cell lines such as SP2/0 HEK and particularly Chinese hamster ovary cells. For a long time now, most investigations have been focused on increasing host cell productivity using genetic manipulating of cellular processes like cell cycle, apoptosis, cell growth, protein secretory and other pathways. In recent decades MicroRNAs beside different genetic engineering tools (e.g., TALEN, ZFN, and Crisper/Cas) have attracted further attention as a tool in the genetic engineering of host cells to increase protein expression levels. Their ability to simultaneously target multiple mRNAs involved in one or more cellular processes made them a favorable tool in this field. Accordingly, this study aimed to review the methods of selecting target miRNA for cell line engineering, miRNA gain- or loss-of-function strategies, examples of laboratory and pilot studies in this field and discussed advantages and disadvantages of this technology.
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