Wajih Nadeem, Hutson Susan M, Wallin Reidar
Department of Internal Medicine, Wake Forest University School of Medicine, Medical Center BLV, Winston-Salem, NC 27157, USA.
Blood. 2006 Dec 1;108(12):3757-60. doi: 10.1182/blood-2006-02-004671. Epub 2006 Aug 10.
To improve production of functional fully gamma-carboxylated recombinant human clotting factor IX (r-hFIX), cell lines stably overexpressing r-hFIX have been engineered to also overexpress proteins of the gamma-carboxylation system. Here we demonstrate that siRNA silencing of calumenin, an inhibitor of the gamma-carboxylation system, enhances production of functional r-hFIX produced by engineered BHK21 cells. The production yield of functional r-hFIX was 80% in engineered cells where calumenin had been silenced 78%. We propose that this high-yield expression system can easily be adapted to overproduce functional forms of all members of the vitamin K-dependent protein family.
为提高功能性全γ-羧化重组人凝血因子IX(r-hFIX)的产量,已构建稳定过表达r-hFIX的细胞系,使其同时过表达γ-羧化系统的蛋白质。在此,我们证明,γ-羧化系统的抑制剂钙网蛋白(calumenin)的siRNA沉默可提高经工程改造的BHK21细胞产生的功能性r-hFIX的产量。在钙网蛋白沉默率为78%的工程细胞中,功能性r-hFIX的产量为80%。我们提出,这种高产表达系统可轻松改造用于过量生产维生素K依赖蛋白家族所有成员的功能形式。