Diederich Patrick, Hoffmann Marc, Hubbuch Jürgen
Inst. of Engineering in Life Sciences, Section IV: Biomolecular Separation Engineering, Karlsruhe Institute of Technology (KIT), Karlsruhe, Germany.
Biotechnol Prog. 2015 Jul-Aug;31(4):957-73. doi: 10.1002/btpr.2104. Epub 2015 May 27.
With an increased number of applications in the field of the avidin-biotin technology, the resulting demand for highly-purified protein avidin has drawn our attention to the purification process of avidin that naturally occurs in chicken egg white. The high-throughput process development (HTPD) methodology was exploited, in order to evaluate purification process alternatives to commonly used ion-exchange chromatography. In a high-throughput format, process parameters for aqueous two-phase extraction, selective precipitation with salts and polyethylene glycol, and hydrophobic interaction and mixed-mode column chromatography experiments were performed. The HTPD strategy was complemented by a high-throughput tandem high-performance liquid chromatography assay for protein quantification. Suitable conditions for the separation of avidin from the major impurities ovalbumin, ovomucoid, ovotransferrin, and lysozyme were identified in the screening experiments. By combination of polyethylene glycol precipitation with subsequent resolubilization and separation in a polyethylene glycol/sulfate/sodium chloride two-phase system an avidin purity of 77% was obtained with a yield >90% while at the same time achieving a significant reduction of the process volume. The two-phase extraction and precipitation results were largely confirmed in larger scale with scale-up factors of 230 and 133, respectively. Seamless processing of the avidin enriched bottom phase was found feasible by using mixed-mode chromatography. By gradient elution a final avidin purity of at least 97% and yield >90% was obtained in the elution pool. The presented identification of a new and beneficial alternative for the purification of the high value protein thus represents a successful implementation of HTPD for an industrially relevant purification task.
随着抗生物素蛋白-生物素技术在该领域的应用数量不断增加,对高纯度抗生物素蛋白的需求促使我们关注鸡蛋白中天然存在的抗生物素蛋白的纯化过程。我们采用了高通量工艺开发(HTPD)方法,以评估替代常用离子交换色谱法的纯化工艺。以高通量形式进行了双水相萃取、用盐和聚乙二醇进行选择性沉淀、疏水相互作用以及混合模式柱色谱实验的工艺参数研究。HTPD策略辅以用于蛋白质定量的高通量串联高效液相色谱分析。在筛选实验中确定了从主要杂质卵清蛋白、卵类粘蛋白、转铁蛋白和溶菌酶中分离抗生物素蛋白的合适条件。通过聚乙二醇沉淀与随后在聚乙二醇/硫酸盐/氯化钠双水相系统中复溶和分离相结合,获得了纯度为77%、产率>90%的抗生物素蛋白,同时实现了工艺体积的显著减少。双水相萃取和沉淀结果在较大规模上分别以230和133的放大因子得到了很大程度的证实。通过使用混合模式色谱法发现对富含抗生物素蛋白的下层相进行无缝处理是可行的。通过梯度洗脱,在洗脱池中获得了最终抗生物素蛋白纯度至少为97%且产率>90%的结果。因此,所提出的用于纯化高价值蛋白质的新的有益替代方法代表了HTPD在工业相关纯化任务中的成功应用。