通过使用杆状病毒表达载体系统(BEVS),已经使得在昆虫细胞中产生重组蛋白成为可能。尽管许多蛋白质通过这个平台取得了成功,由于细胞病变效应等问题,一些目标仍然是一个挑战,共感染和共表达的不可预测性质,和杆状病毒基因组不稳定。为了在昆虫细胞中表达不同的蛋白质,已经测定了许多启动子。然而,在审查市售杆状病毒载体的情况时,这些结果仍然缺乏实施。在推进平台生产更多种类的蛋白质和复合物的过程中,这种结构的发展是不可避免的。更好地了解病毒基因调控和启动子选择,包括病毒,合成,和昆虫来源的启动子将有利于研究人员通过招募这些复杂的基因调控机制来利用BEVS进行异源基因表达。在这里,我们总结了一些可用于改善重组蛋白和多蛋白复合物在昆虫细胞中表达的进展。
Generating recombinant proteins in insect cells has been made possible via the use of the
Baculovirus Expression Vector System (BEVS). Despite the success of many proteins via this platform, some targets remain a challenge due to issues such as cytopathic effects, the unpredictable nature of co-infection and co-expressions, and
baculovirus genome instability. Many promoters have been assayed for the purpose of expressing diverse proteins in insect cells, and yet there remains a lack of implementation of those results when reviewing the landscape of commercially available
baculovirus vectors. In advancing the platform to produce a greater variety of proteins and complexes, the development of such constructs cannot be avoided. A better understanding of viral gene regulation and promoter options including viral, synthetic, and insect-derived promoters will be beneficial to researchers looking to utilize BEVS by recruiting these intricate mechanisms of gene regulation for heterologous gene expression. Here we summarize some of the developments that could be utilized to improve the expression of recombinant proteins and multi-protein complexes in insect cells.