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首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >A simple and rapid method to monitor the disassembly and reassembly of virus-like particles
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A simple and rapid method to monitor the disassembly and reassembly of virus-like particles

机译:一种简单快速的方法来监视病毒样颗粒的拆卸和重新组装

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摘要

Protein fluorescence spectra (?300-440 nm) could be used as a simple and sensitive method to monitor the disassembly and reassembly of virus-like particles (VLPs). Insect cell expressed and purified HPV-16 L1 VLPs show significantly high fluorescence intensity, whereas the fluorescence is almost quenched after disassembly by adding the reducing agent. By removing the reducing agent, the fluorescence was restored to its original intensity, indicating the reassembly of VLPs. The data are consistent with enzyme-linked immunosorbent assay (ELISA) reactivity using conformation-specific mouse monoclonal antibody. The same method could be extended to VLPs of other viruses.
机译:蛋白荧光光谱(约300-440 nm)可以用作一种简单而灵敏的方法来监测病毒样颗粒(VLP)的拆卸和重新组装。昆虫细胞表达和纯化的HPV-16 L1 VLP表现出明显高的荧光强度,而通过添加还原剂分解后荧光几乎被淬灭。通过除去还原剂,荧光恢复到其原始强度,表明VLP重新组装。数据与使用构象特异性小鼠单克隆抗体的酶联免疫吸附测定(ELISA)反应性一致。相同的方法可以扩展到其他病毒的VLP。

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