Katagiri Nobuyuki, Shimokawa Daisuke, Suzuki Takayuki, Kousai Masahito, Iritani Eiji
Department of Environmental Technology, Meijo University, 1-501 Shiogamaguchi, Tempaku-ku, Nagoya 468-8502, Japan.
Department of Chemical Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Japan.
Membranes (Basel). 2023 Jan 29;13(2):168. doi: 10.3390/membranes13020168.
Plasmid DNA is used as a vector for gene therapy and DNA vaccination; therefore, the establishment of a mass production method is required. Membrane filtration is widely employed as a separation method suitable for the mass production of plasmid DNA. Furthermore, the separation of plasmid DNA using microfiltration and ultrafiltration membranes is being investigated. Because plasmid DNA has a circular structure, it undergoes significant deformation during filtration and easily permeates the membrane, hindering the selection of separation membranes based on molecular weight. In this study, we applied affinity microfiltration to plasmid DNA purification. -FeO with an isoelectric point of approximately 8 and a particle size of 0.5 μm was selected as the ligand for two-stage affinity microfiltration of plasmid DNA. In the first stage of microfiltration, the experiment was conducted at a pH of 5, and a cake of -FeO with bound plasmid DNA was obtained. Next, liquid permeation (pH 9 and 10) through the cake was performed to elute the bound plasmid DNA. Plasmid DNA was eluted during the early phase of liquid permeation at pH 10. Furthermore, agarose gel analysis confirmed the usefulness of the two-stage affinity microfiltration method with adsorption and desorption for plasmid DNA purification.
质粒DNA被用作基因治疗和DNA疫苗接种的载体;因此,需要建立大规模生产方法。膜过滤作为一种适用于质粒DNA大规模生产的分离方法被广泛应用。此外,利用微滤膜和超滤膜分离质粒DNA的研究也在进行。由于质粒DNA具有环状结构,在过滤过程中会发生显著变形,容易透过膜,这阻碍了基于分子量来选择分离膜。在本研究中,我们将亲和微滤应用于质粒DNA的纯化。选择等电点约为8、粒径为0.5μm的-FeO作为质粒DNA两步亲和微滤的配体。在微滤的第一阶段,实验在pH为5的条件下进行,得到了结合有质粒DNA的-FeO滤饼。接下来,进行透过滤饼的液体渗透(pH为9和10)以洗脱结合的质粒DNA。在pH为10的液体渗透早期阶段洗脱了质粒DNA。此外,琼脂糖凝胶分析证实了具有吸附和解吸作用的两步亲和微滤法用于质粒DNA纯化的有效性。