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Concentration and purification of enterovirus 71 using a weak anion-exchange monolithic column

机译:使用弱阴离子交换整体柱对肠道病毒71进行浓缩和纯化

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Background Enterovirus 71 (EV-71) is a neurotropic virus causing Hand, Foot and Mouth Disease (HFMD) in infants and children under the age of five. It is a major concern for public health issues across Asia-Pacific region. The most effective way to control the disease caused by EV-71 is by vaccination thus a novel vaccine is urgently needed. Inactivated EV-71 induces a strong, virus-neutralizing antibody response in animal models, protecting them against a lethal EV-71 challenge and it has been shown to elicit cross-neutralizing antibodies in human trials. Hence, the large-scale production of purified EV-71 is required for vaccine development, diagnosis and clinical trials. Methods CIM? Monolith columns are single-piece columns made up of poly(glycidyl methacrylate co-ethylene dimethacrylate) as support matrix. They are designed as porous channels rather than beads with different chemistries for different requirements. As monolithic columns have a high binding capacity, flow rate and resolution, a CIM? DEAE-8f tube monolithic column was selected for purification in this study. The EV-71 infected Rhabdomyosarcoma (RD) cell supernatant was concentrated using 8% PEG 8000 in the presence of 400?mM sodium chloride. The concentrated virus was purified by weak anion exchange column using 50?mM HEPES?+?1?M sodium chloride as elution buffer. Results Highly pure viral particles were obtained at a concentration of 350?mM sodium chloride as confirmed by SDS-PAGE and electron microscopy. Presence of viral proteins VP1, VP2 and VP3 was validated by western blotting. The overall process achieved a recovery of 55%. Conclusions EV-71 viral particles of up to 95% purity can be recovered by a single step ion-exchange chromatography using CIM-DEAE monolithic columns and 1?M sodium chloride as elution buffer. Moreover, this method is scalable to purify several litres of virus-containing supernatant, using industrial monolithic columns with a capacity of up to 8?L such as CIM? cGMP tube monolithic columns.
机译:背景肠病毒71(EV-71)是一种神经营养性病毒,可引起五岁以下婴幼儿手足口病(HFMD)。这是整个亚太地区公共卫生问题的主要关注点。控制EV-71引起的疾病的最有效方法是接种疫苗,因此迫切需要一种新型疫苗。灭活的EV-71在动物模型中诱导了强烈的,病毒中和的抗体反应,从而保护了它们免于致命的EV-71攻击,并且在人体试验中已证明可引起交叉中和的抗体。因此,疫苗开发,诊断和临床试验需要大规模生产纯化的EV-71。方法CIM ?整体柱是由聚(甲基丙烯酸缩水甘油酯和二甲基丙烯酸乙二酯)组成的单件式色谱柱。它们被设计为多孔通道,而不是针对不同要求具有不同化学性质的珠子。由于整体柱具有较高的结合能力,流速和分离度,本研究选择了CIM α DEAE-8f管整体柱进行纯化。在400?mM氯化钠存在下,使用8%PEG 8000浓缩被EV-71感染的横纹肌肉瘤(RD)细胞上清液。浓缩的病毒通过弱阴离子交换柱用50μmHEPES 2 +1μM氯化钠作为洗脱缓冲液纯化。结果通过SDS-PAGE和电子显微镜证实,可以得到浓度为350?mM氯化钠的高纯度病毒颗粒。通过蛋白质印迹验证了病毒蛋白VP1,VP2和VP3的存在。整个过程实现了55%的回收率。结论使用CIM-DEAE整体柱和1?M氯化钠作为洗脱缓冲液,通过一步离子交换色谱可以回收纯度高达95%的EV-71病毒颗粒。此外,该方法可扩展至纯化容量达8 µL的工业整体柱,例如CIM ? cGMP管整体柱,从而纯化数升含病毒的上清液。

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