Laboratoire de Biologie Moléculaire, Ecole de Biologie Industrielle, 32 Boulevard du port, 95094, Cergy-Pontoise cedex, France.
Mol Biotechnol. 2013 Nov;55(3):227-35. doi: 10.1007/s12033-013-9673-5.
In this work, a multifunctional expression cassette, termed Multitags, combining different and complementary functionalities, was designed and used to monitor the expression and the purification of two model proteins (Pfu DNA polymerase and Myosin-VIIa- and Rab-Interracting protein : MyRIP). Multitags contains two affinity purification tags, a polyhistidine sequence (10× His) and the streptavidin-binding peptide (SBP) and as a marker tag the heme-binding domain of rat cytochrome b5 followed by the TEV cleavage site. Using the Multitags as fusion partner, more than 90 % of both fusion proteins were produced in soluble form when expressed in Escherichia coli KRX. In addition, high purity (99 %) of recombinant proteins was achieved after two consecutive affinity purification steps. The expression cassette also demonstrated an accurate monitoring capability comparable to that of a dual recognition-based method. The choice of the SBP tag was considered as an integral process that included a method for tag removal. Thus, an immobilized TEV protease fixed on streptavidin-agarose matrix was used for the cleavage of fusion proteins. After digestion, both unprocessed fusion proteins and Multitags were retained on the proteolytic column via their SBP sequence, allowing cleavage and recovery of target proteins on one step. This combined approach may accelerate the development of optimized production processes, while insuring high product quality and a low production cost.
在这项工作中,设计并使用了一种多功能表达盒,称为 Multitags,它结合了不同且互补的功能,用于监测两种模型蛋白(Pfu DNA 聚合酶和肌球蛋白-VIIa 和 Rab 相互作用蛋白:MyRIP)的表达和纯化。Multitags 包含两个亲和纯化标签,一个组氨酸序列(10×His)和链霉亲和素结合肽(SBP),以及大鼠细胞色素 b5 的血红素结合结构域作为标记标签,后面是 TEV 切割位点。使用 Multitags 作为融合伴侣,当在大肠杆菌 KRX 中表达时,两种融合蛋白的可溶性形式都超过 90%。此外,经过连续两次亲和纯化步骤,可获得 99%的高纯度重组蛋白。该表达盒还表现出与基于双重识别的方法相当的准确监测能力。SBP 标签的选择被认为是一个完整的过程,包括标签去除的方法。因此,固定在链霉亲和素琼脂糖基质上的固定化 TEV 蛋白酶用于融合蛋白的切割。消化后,通过它们的 SBP 序列,未加工的融合蛋白和 Multitags 都保留在蛋白水解柱上,允许在一步中切割和回收靶蛋白。这种组合方法可以加速优化生产工艺的开发,同时确保产品质量高、生产成本低。