ENEA, Dipartimento BIOTEC, Sezione Genetica e Genomica Vegetale, C.R. Casaccia, Via Anguillarese 301, 00123, Rome, Italy.
Transgenic Res. 2010 Dec;19(6):1083-97. doi: 10.1007/s11248-010-9382-9. Epub 2010 Mar 15.
It was previously demonstrated that the tumour-targeting antibody mAb H10 can be transiently expressed and purified at high levels in Nicotiana benthamiana by using a vacuum-agroinfiltration system boosted by the use of a virus silencing suppressor protein. Scope of this work was to analyse different steps of protein extraction from agroinfiltrated leaves to optimise the purification process of the secretory mAb H10 providing new insights in the field of large-scale plant production. Two different extraction procedures (mechanical shearing/homogenisation and recovery of intercellular fluids -IFs-) were evaluated and compared in terms of purified antibody yields, antibody degradation and total phenolic compounds content. Mechanical grinding from fresh leaf tissues gave the highest purification yield (75 mg/kg Fresh Weight -75% intact tetrameric IgG-) and total phenolics concentration in the range of 420 μg/g FW. The second extraction procedure, based on the recovery of IFs, gave purification yields of 15-20 mg/kg FW (corresponding to 27% of total soluble protein) in which about 40% of purified protein is constituted by fully assembled IgG with a total phenolic compounds content reduced by one order of magnitude (21 μg/g FW). Despite a higher antibody degradation, purification from intercellular fluids demonstrated to be very promising since extraction procedures resulted extremely fast and amenable to scaling-up. Overall data highlight that different extraction procedures can dramatically affect the proteolytic degradation and quality of antibody purified from agroinfiltrated N. benthamiana leaves. Based on these results, we optimised a pilot-scale purification protocol using a two-step purification procedure from batches of fresh agroinfiltrated leaves (250 g) allowing purification of milligram quantities (average yield 40 mg/kg FW) of fully assembled and functional IgG with a 99.4% purity, free of phenolic and alkaloid compounds with low endotoxin levels (<1 EU/ml).
先前的研究表明,通过使用病毒沉默抑制蛋白增强的真空-农杆菌浸润系统,可以在本氏烟中瞬时高水平表达和纯化肿瘤靶向抗体 mAb H10。本研究的目的是分析从农杆菌浸润叶片中提取蛋白质的不同步骤,以优化分泌型 mAb H10 的纯化过程,为大规模植物生产领域提供新的见解。评估和比较了两种不同的提取程序(机械剪切/匀浆和回收细胞间液-IFs-),从纯化抗体产量、抗体降解和总酚含量方面进行比较。从新鲜叶片组织进行机械研磨可获得最高的纯化产量(75mg/kg 鲜重-75%完整四聚体 IgG-)和总酚浓度在 420μg/gFW 范围内。基于 IFs 回收的第二种提取方法,可获得 15-20mg/kgFW 的纯化产量(对应于总可溶性蛋白的 27%),其中约 40%的纯化蛋白由完全组装的 IgG 组成,总酚含量降低了一个数量级(21μg/gFW)。尽管抗体降解率较高,但从细胞间液中进行纯化具有很大的前景,因为提取方法非常快速且易于扩大规模。总体数据表明,不同的提取方法可能会对从农杆菌浸润的本氏烟叶片中纯化的抗体的蛋白水解降解和质量产生巨大影响。基于这些结果,我们优化了一个使用两步纯化程序从新鲜农杆菌浸润叶片(250g)批次进行中试规模纯化的方案,允许纯化毫克数量(平均产量 40mg/kgFW)的完全组装和功能 IgG,纯度为 99.4%,无酚类和生物碱化合物,内毒素水平低(<1EU/ml)。