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Purification of recombinant nucleocapsid protein of Newcastle disease virus from unclarified feedstock using expanded bed adsorption chromatography

机译:使用扩展床吸附色谱法从未澄清的原料中纯化新城疫病毒的重组核衣壳蛋白

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摘要

In the present work, a single-step purification of recombinant nucleocapsid protein (NP) of the Newcastle disease virus (NDV) directly from unclarified feedstock using an expanded bed adsorption chromatography (EBAC) was developed. Streamline 25 column (ID = 25 mm) was used as a contactor and Streamline chelating adsorbent immobilized with Ni ion was used as affinity adsorbent. The dynamic binding capacity of Ni -loaded Streamline chelating adsorbent for the NP protein in unclarified feedstock was found to be 2.94 mg ml adsorbent at a superficial velocity of 200 cm h . The direct purification of NP protein from unclarified feedstock using expanded bed adsorption has resulted in a 31% adsorption and 9.6% recovery of NP protein. The purity of the NP protein recovered was about 70% and the volume of processing fluid was reduced by a factor of 10. The results of the present study show that the IMA-EBAC developed could be used to combine the clarification, concentration and initial purification steps into a single-step operation.
机译:在目前的工作中,开发了使用扩展床吸附色谱法(EBAC)直接从未澄清的原料中一步纯化纯化新城疫病毒(NDV)的重组核衣壳蛋白(NP)。使用Streamline 25色谱柱(ID = 25 mm)作为接触器,并使用固定有Ni离子的Streamline螯合吸附剂作为亲和吸附剂。在表面速度为200 cm h的条件下,Ni负载的Streamline螯合吸附剂对NP蛋白的动态结合能力为2.94 mg ml吸附剂。使用扩展床吸附技术直接从未澄清的原料中纯化NP蛋白,可实现31%的吸附和9.6%的NP蛋白回收率。回收的NP蛋白纯度约为70%,加工液体积减少了10倍。本研究结果表明,开发的IMA-EBAC可用于澄清,浓缩和初始纯化的结合单步操作。

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