Kralj Špela, Kodermac Špela Meta, Bergoč Ines, Kostelec Tomas, Podgornik Aleš, Štrancar Aleš, Černigoj Urh
Sartorius BIA Separations d.o.o., Ajdovščina, Slovenia.
Department of Chemical Engineering and Technical Safety, Faculty of Chemistry and Chemical Technology, University of Ljubljana, Ljubljana, Slovenia.
Electrophoresis. 2023 Dec;44(24):1953-1966. doi: 10.1002/elps.202300035. Epub 2023 Jun 4.
Increased need for plasmid DNA (pDNA) with sizes above 10 kbp (large pDNA) in gene therapy and vaccination brings the need for its large-scale production with high purity. Chromatographic purification of large pDNA is often challenging due to low process yields and column clogging, especially using anion-exchanging columns. The goal of our investigation was to evaluate the mass balance and pDNA isoform composition at column outlet for plasmids of different sizes in combination with weak anion exchange (AEX) monolith columns of varying channel size (2, 3 and 6 µm channel size). We have proven that open circular pDNA (OC pDNA) isoform is an important driver of reduced chromatographic performance in AEX chromatography. The main reason for the behaviour is the entrapment of OC pDNA in chromatographic supports with smaller channel sizes. Entrapment of individual isoforms was characterised for porous beads and convective monolithic columns. Convective entrapment of OC pDNA isoform was confirmed on both types of stationary phases. Porous beads in addition showed a reduced recovery of supercoiled pDNA (on an 11.6 kbp plasmid) caused by diffusional entrapment within the porous structure. Use of convective AEX monoliths or membranes with channel diameter >3.5 µm has been shown to increase yields and prevent irreversible pressure build-up and column clogging during purification of plasmids at least up to 16 kbp in size.
在基因治疗和疫苗接种中,对大于10千碱基对(大质粒DNA)的质粒DNA(pDNA)的需求增加,这就需要大规模生产高纯度的pDNA。大pDNA的色谱纯化通常具有挑战性,因为工艺产率低且柱堵塞,特别是使用阴离子交换柱时。我们研究的目的是结合不同通道尺寸(2、3和6微米通道尺寸)的弱阴离子交换(AEX)整体柱,评估不同大小质粒在柱出口处的质量平衡和pDNA异构体组成。我们已经证明,开环pDNA(OC pDNA)异构体是AEX色谱中色谱性能降低的一个重要驱动因素。这种行为的主要原因是OC pDNA被困在通道尺寸较小的色谱支持物中。对多孔珠和对流整体柱中单个异构体的截留进行了表征。在两种类型的固定相上都证实了OC pDNA异构体的对流截留。多孔珠还显示,由于在多孔结构内的扩散截留,超螺旋pDNA(在11.6千碱基对的质粒上)的回收率降低。已表明,使用通道直径大于3.5微米的对流AEX整体柱或膜可提高产率,并防止在纯化至少达16千碱基对大小的质粒期间不可逆转的压力积累和柱堵塞。