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Oxidative protein refolding on size exclusion chromatography: From batch single-column to multi-column counter-current continuous processing

机译:尺寸排阻色谱法上的氧化性蛋白重折叠:从分批单柱到多柱逆流连续处理

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Recently protein refolding on size exclusion chromatography (SEC) operated in multi-column continuous simulated moving bed (SMB) configurations (hereinafter SMB-SEC) has been investigated for future industrial applications. This is due to several advantages offered by SMB configurations particularly when process parameters are thoroughly screened and optimized. A robust mathematical model is essential for high-throughput process screening and optimization. In this work, a previously investigated single-column mathematical model was modified to extend its applicability for protein oxidative refolding/aggregation predictions in SMB-SEC. The model considers a wide loading concentration range of the model protein (lysozyme) on SEC. The potential influences of high concentrations of chaotropic reagents on kinetic and thermodynamic model parameters have been discussed based on previous experimental results and their predicted local concentrations through the SMB-SEC columns and at the product stream. It was observed that aggregation occurs when local protein concentration exceeds a critical concentration. No urea recovery at the product stream indicated that the refolding reaction will continue off-column to recover the native-protein product. Therefore, it is suggested that the developed model is tested against experimental results for total soluble protein (early intermediates and native conformations) in the presence of L-arginine additive and process performance indicators are defined based on this criterion. (C) 2015 Elsevier Ltd. All rights reserved.
机译:近来,已经研究了在多柱连续模拟移动床(SMB)构造(以下称为SMB-SEC)中操作的尺寸排阻色谱法(SEC)上的蛋白质复性,以用于未来的工业应用。这是由于SMB配置提供的几个优点,特别是在彻底筛选和优化过程参数时。强大的数学模型对于高通量过程筛选和优化至关重要。在这项工作中,对以前研究的单列数学模型进行了修改,以扩展其在SMB-SEC中蛋白质氧化重折叠/聚集预测中的适用性。该模型考虑了SEC上模型蛋白(溶菌酶)的较大负载浓度范围。基于以前的实验结果以及通过SMB-SEC色谱柱和产物流预测的局部浓度,讨论了高浓度离液剂对动力学和热力学模型参数的潜在影响。观察到当局部蛋白质浓度超过临界浓度时发生聚集。在产物流处没有尿素回收表明再折叠反应将继续在柱外进行以回收天然蛋白产物。因此,建议在存在L-精氨酸添加剂的情况下,针对总可溶性蛋白(早期中间体和天然构象)的实验结果对开发的模型进行测试,并基于此标准定义过程性能指标。 (C)2015 Elsevier Ltd.保留所有权利。

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