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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Adsorption of virus-like particles on ion exchange surface: Conformational changes at different pH detected by dual polarization interferometry
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Adsorption of virus-like particles on ion exchange surface: Conformational changes at different pH detected by dual polarization interferometry

机译:离子交换表面上病毒样颗粒的吸附:通过双极化干涉仪检测到的不同pH下的构象变化

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摘要

Disassembling of virus-like particles (VLPs) like hepatitis B virus surface antigen (HB-VLPs) during chromatographic process has been identified as a major cause of loss of antigen activity. In this study, dual polarization interferometry (DPI) measurement, together with chromatography experiments, were performed to study the adsorption and conformational change of HB-VLPs on ion exchange surface at three different pHs. Changes in pH values of buffer solution showed only minimal effect on the HB-VLPs assembly and antigen activity, while significantly different degree of HB-VLPs disassembling was observed after ion exchange chromatography (IEC) at different pHs, indicating the conformational change of HB-VLPs caused mainly by its interactions with the adsorbent surface. By creating an ion exchange surface on chip surface, the conformational changes of HB-VLPs during adsorption to the surface were monitored in real time by DPI for the first time. As pH increased from 7.0 to 9.0, strong electrostatic interactions between oppositely charged HB-VLPs and the ion exchange surface make the HB-VLPs spread thinly or even adsorbed in disassembled formation on the surface as revealed by significant decrease in thickness of the adsorbed layer measured by DPI. Such findings were consistent with the results of IEC experiments operated at different pHs, that more disassembled HB-VLPs were detected in the eluted proteins at pH 9.0. At low pH like pH 5.0, however, possible hi-layer adsorption was involved as evidenced by an adsorbed layer thickness higher than average diameter of the HB-VLPs. The "lateral" protein protein interactions might be unfavorable and would make additional contribution to the disassembling of HB-VLPs besides the primary mechanism related to the protein surface interactions; therefore, the lowest antigen activity was observed after IEC at pH 5.0. Such real-time information on conformational change of VLPs is helpful for better understanding the real mechanism for the disassembling of VLPs on the solid liquid interface. (C) 2015 Elsevier B.V. All rights reserved.
机译:色谱过程中像乙型肝炎病毒表面抗原(HB-VLPs)这样的病毒样颗粒(VLP)的拆卸已被确定为抗原活性丧失的主要原因。在这项研究中,进行了双极化干涉法(DPI)测量和色谱实验,以研究在三个不同pH值下HB-VLP在离子交换表面的吸附和构象变化。缓冲溶液pH值的变化对HB-VLPs组装和抗原活性的影响很小,而离子交换色谱法(IEC)在不同pHs下观察到的HB-VLPs分解程度明显不同,表明HB-VLP的构象变化VLP主要由其与吸附剂表面的相互作用引起。通过在芯片表面上创建离子交换表面,首次通过DPI实时监测了HB-VLP吸附到表面期间的构象变化。当pH从7.0增加到9.0时,带相反电荷的HB-VLP与离子交换表面之间的强静电相互作用使HB-VLP稀薄地分散甚至被吸附在表面上以分解形式被吸附,这通过测量的被吸附层厚度的显着减小来揭示。由DPI。这些发现与在不同pH下进行的IEC实验结果一致,即在pH 9.0的洗脱蛋白中检测到更多的拆解的HB-VLP。但是,在低pH值(如pH 5.0)下,可能会发生高层吸附,这是由高于HB-VLP的平均直径的吸附层厚度所证明的。 “横向”蛋白质蛋白质相互作用可能是不利的,除了与蛋白质表面相互作用有关的主要机制外,还将对HB-VLP的分解做出额外贡献。因此,IEC在pH 5.0下观察到最低的抗原活性。这种有关VLP构象变化的实时信息有助于更好地了解在固态液体界面上拆卸VLP的真实机制。 (C)2015 Elsevier B.V.保留所有权利。

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