School of Physical Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Clinical Pathology Center, The First Affiliated Hospital of Anhui Medical University, Hefei 230012, China.
Molecules. 2023 Mar 31;28(7):3132. doi: 10.3390/molecules28073132.
Serratiopeptidase is a clinical therapeutic protein for the treatment of human diseases such as arthritis, bronchitis, and thrombosis. Yet production of this protein in a heterologous host (e.g., ) is difficult due to the issue of protein insolubility and the requirement of laborious refolding procedures. Cell-free protein synthesis (CFPS) systems, derived from crude cell extracts, are effective platforms for the expression of recombinant proteins in vitro. Here, we report a new method to produce serratiopeptidase by using an -based CFPS system. After rational selection of cell extracts and construction of expression vectors, soluble expression of serratiopeptidase was achieved and the enzyme activity could be readily tested in the cell-free reaction mixture. By further optimizing the key parameters, optimum conditions for the enzyme activity assay were obtained, including the pH value at 5, reaction temperature at 45 °C, substrate concentration at 10 mg/mL, and supplementing Ca ions at 5 mM. Moreover, the CFPS mixture was freeze-dried and the activity of serratiopeptidase could be regenerated by hydration without losing activity. Overall, the CFPS system enabled soluble expression of serratiopeptidase with catalytic activity, providing a new and promising approach for this enzyme production. Our work extends the utility of the cell-free platform to produce therapeutic proteins with clinical applications.
糜蛋白酶是一种临床治疗人类疾病的治疗性蛋白,如关节炎、支气管炎和血栓形成。然而,由于蛋白质的不溶性和费力的重折叠过程的要求,这种蛋白质在异源宿主(例如)中的生产是困难的。无细胞蛋白质合成(CFPS)系统源自粗细胞提取物,是体外表达重组蛋白的有效平台。在这里,我们报告了一种使用基于 - 的 CFPS 系统生产糜蛋白酶的新方法。经过细胞提取物的合理选择和表达载体的构建,实现了糜蛋白酶的可溶性表达,并且可以在无细胞反应混合物中轻松测试酶活性。通过进一步优化关键参数,获得了酶活性测定的最佳条件,包括 pH 值为 5、反应温度为 45°C、底物浓度为 10mg/mL 和补充 5mM 的 Ca 离子。此外,CFPS 混合物可以冻干,并且糜蛋白酶的活性可以通过水合再生而不会失去活性。总的来说,CFPS 系统实现了具有催化活性的糜蛋白酶的可溶性表达,为这种酶的生产提供了一种新的、有前途的方法。我们的工作扩展了无细胞平台的用途,以生产具有临床应用的治疗性蛋白质。