Nasimuzzaman Md, van der Loo Johannes C M, Malik Punam
Division of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center; University of Cincinnati College of Medicine;
Division of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center; University of Cincinnati College of Medicine; Raymond G. Perelman Center for Cellular and Molecular Therapeutics, The Children's Hospital of Philadelphia.
J Vis Exp. 2018 Apr 9(134):57019. doi: 10.3791/57019.
Baculovirus has traditionally been used for the production of recombinant protein and vaccine. However, more recently, baculovirus is emerging as a promising vector for gene therapy application. Here, baculovirus is produced by transient transfection of the baculovirus plasmid DNA (bacmid) in an adherent culture of Sf9 cells. Baculovirus is subsequently expanded in Sf9 cells in a serum-free suspension culture until the desired volume is obtained. It is then purified from the culture supernatant using heparin affinity chromatography. Virus supernatant is loaded onto the heparin column which binds baculovirus particles in the supernatant due to the affinity of heparin for baculovirus envelop glycoprotein. The column is washed with a buffer to remove contaminants and baculovirus is eluted from the column with a high-salt buffer. The eluate is diluted to an isotonic salt concentration and baculovirus particles are further concentrated using ultracentrifugation. Using this method, baculovirus can be concentrated up to 500-fold with a 25% recovery of infectious particles. Although the protocol described here demonstrates the production and purification of the baculovirus from cultures up to 1 L, the method can be scaled-up in a closed-system suspension culture to produce a clinical-grade vector for gene therapy application.
杆状病毒传统上一直用于生产重组蛋白和疫苗。然而,最近杆状病毒正成为一种有前途的基因治疗应用载体。在此,杆状病毒通过在Sf9细胞的贴壁培养物中瞬时转染杆状病毒质粒DNA(杆粒)来产生。随后杆状病毒在无血清悬浮培养的Sf9细胞中扩增,直至获得所需体积。然后使用肝素亲和色谱法从培养上清液中纯化。将病毒上清液加载到肝素柱上,由于肝素对杆状病毒包膜糖蛋白的亲和力,该柱会结合上清液中的杆状病毒颗粒。用缓冲液洗涤柱子以去除污染物,并用高盐缓冲液从柱上洗脱杆状病毒。将洗脱液稀释至等渗盐浓度,并使用超速离心进一步浓缩杆状病毒颗粒。使用这种方法,杆状病毒可以浓缩至500倍,感染性颗粒的回收率为25%。尽管此处描述的方案展示了从高达1升的培养物中生产和纯化杆状病毒,但该方法可在封闭系统悬浮培养中扩大规模,以生产用于基因治疗应用的临床级载体。