摘要
为了解决骨形态发生蛋白10(bone morphogenetic protein 10,BMP10)前体蛋白proBMP10在中国仓鼠卵巢(CHO)细胞中由于Furin导致的表达产物不均一问题,构建了proBMP10在Furin酶切识别位点处的突变体proBMP10-1(R313K)和proBMP10-2(R316K),并分别将目的基因定点整合进CHO-K1-BAK-/BAX-基因组,成功构建了稳定表达目标蛋白质的重组CHO细胞株。结果表明,proBMP10-2 (R316K)不再被Furin切割,且具有生物活性,而proBMP10-1(R313K)仍然会被Furin切割。
To address the issue of heterogeneous expression products derived from proBMP10(the precursor protein of bone morphogenetic protein 10,BMP10)in Chinese hamster ovary(CHO)cells caused by Furin,the mutations of proBMP10 at its Furin recognition sites,proBMP10-1(R313K)and proBMP10-2(R316K),were constructed and site-directedly integrated into the genome of CHO-K1-BAK-/BAX-respectively.The recombinant CHO cell lines stably expressing the target proteins were successfully established.The results showed that the proBMP10-2(R316K)was no longer cleaved by Furin and retained biological activity,while proBMP10-1(R313K)continued to be cleaved by Furin.
作者
段珂
段作营
金坚
DUAN Ke;DUAN Zuoying;JIN Jian(School of Biotechnology,Jiangnan University,Wuxi 214122,China;School of Life Sciences and Health Engineering,Jiangnan University,Wuxi 214122,China)
出处
《食品与生物技术学报》
CAS
CSCD
北大核心
2024年第1期106-112,共7页
Journal of Food Science and Biotechnology
关键词
骨形态发生蛋白10
突变体
定点整合
bone morphogenetic protein 10
mutant
site-specific integration