Purification of viruses by electrophoresis in sucrose concentration gradients. 1972.

A Polson
{"title":"Purification of viruses by electrophoresis in sucrose concentration gradients. 1972.","authors":"A Polson","doi":"10.1080/10826069308544534","DOIUrl":null,"url":null,"abstract":"<p><p>Zone electrophoresis (ZE) in concentration gradients of sucrose proved to be a powerful technique in the purification of viruses although it is seldomly used as a single step for the separation of the infective agent from extraneous matter but usually as a final procedure. No difficulties were experienced in the purification of plant viruses with ZE possibly because of the resistance of the agents to the chloroform butanol treatment which the impure plant viruses received prior to the ZE. Likewise no difficulties were encountered during purification of human and animal picorna viruses because they also are resistant to chloroform or chloroform-butanol treatment prior to ZE. Purification of animal and possibly human reoviridae ZE as a final step is involved as they are associated with or even attached to the host cell membranes which are lipoidal in nature. Because the lipoidal material on the virus has an affinity for organic solvents the virus particles are caught in the emulsion when an extract of the crude virus material is shaken with the organic solvent. With these viruses polyethylene glycol M(r) 6000 (PEG) is often helpful as a means of displacing most of the host proteins as a step in the partial purification prior to ZE. Neurotropic African horse sickness virus which presented many problems to overcome was rendered free of extraneous proteins to the extent that electron micrographs could be made of it. Neurotropic Rift Valley fever virus was similarly difficult to purify as it was always associated with mouse brain components. This virus was finally purified from infected mouse blood in which the virus particles were not associated with host cell debris and other extraneous proteins. Zone electrophoresis experiments were not conducted on viruses with large particle sizes e.g. myxoviruses because they could be purified without a great deal of effort using polymer displacement, and thin layer centrifugation. Zone electrophoresis as a means of final purification was vividly displayed with the purification of five viruses of the larvae of the pine emperor moth, Nudaurelia cytheria cytheria.</p>","PeriodicalId":20391,"journal":{"name":"Preparative biochemistry","volume":"23 1-2","pages":"1-30"},"PeriodicalIF":0.0000,"publicationDate":"1993-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/10826069308544534","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Preparative biochemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/10826069308544534","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Zone electrophoresis (ZE) in concentration gradients of sucrose proved to be a powerful technique in the purification of viruses although it is seldomly used as a single step for the separation of the infective agent from extraneous matter but usually as a final procedure. No difficulties were experienced in the purification of plant viruses with ZE possibly because of the resistance of the agents to the chloroform butanol treatment which the impure plant viruses received prior to the ZE. Likewise no difficulties were encountered during purification of human and animal picorna viruses because they also are resistant to chloroform or chloroform-butanol treatment prior to ZE. Purification of animal and possibly human reoviridae ZE as a final step is involved as they are associated with or even attached to the host cell membranes which are lipoidal in nature. Because the lipoidal material on the virus has an affinity for organic solvents the virus particles are caught in the emulsion when an extract of the crude virus material is shaken with the organic solvent. With these viruses polyethylene glycol M(r) 6000 (PEG) is often helpful as a means of displacing most of the host proteins as a step in the partial purification prior to ZE. Neurotropic African horse sickness virus which presented many problems to overcome was rendered free of extraneous proteins to the extent that electron micrographs could be made of it. Neurotropic Rift Valley fever virus was similarly difficult to purify as it was always associated with mouse brain components. This virus was finally purified from infected mouse blood in which the virus particles were not associated with host cell debris and other extraneous proteins. Zone electrophoresis experiments were not conducted on viruses with large particle sizes e.g. myxoviruses because they could be purified without a great deal of effort using polymer displacement, and thin layer centrifugation. Zone electrophoresis as a means of final purification was vividly displayed with the purification of five viruses of the larvae of the pine emperor moth, Nudaurelia cytheria cytheria.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
蔗糖浓度梯度电泳纯化病毒。1972.
蔗糖浓度梯度区带电泳(ZE)被证明是一种强大的病毒纯化技术,尽管它很少被用作分离感染因子与外来物质的单一步骤,但通常作为最后的步骤。用ZE纯化植物病毒没有遇到困难,这可能是由于这些试剂对不纯植物病毒在ZE之前接受的氯仿丁醇处理具有抗性。同样,在纯化人类和动物小核糖核酸病毒时也没有遇到任何困难,因为它们在使用ZE之前也对氯仿或氯仿-丁醇处理具有耐药性。动物和可能的人类呼肠孤病毒的纯化是最后一步,因为它们与宿主细胞膜有关,甚至附着在本质上是脂质的细胞膜上。由于病毒上的脂质物质对有机溶剂有亲和力,当粗病毒物质的提取物与有机溶剂摇晃时,病毒颗粒被捕获在乳剂中。对于这些病毒,聚乙二醇M(r) 6000 (PEG)通常有助于作为取代大多数宿主蛋白的手段,作为在ZE之前部分纯化的一步。嗜神经性非洲马病病毒提出了许多问题需要克服,在电子显微镜下可以使其不含外来蛋白质。嗜神经型裂谷热病毒同样难以纯化,因为它总是与小鼠大脑成分有关。这种病毒最终从受感染的小鼠血液中纯化出来,其中的病毒颗粒不与宿主细胞碎片和其他外来蛋白质相关。对于黏液病毒等大颗粒的病毒,不需要进行区带电泳实验,因为它们可以使用聚合物置换和薄层离心进行纯化,而无需花费大量精力。带电泳作为最终纯化的手段,通过对cytheria cytheria松皇蛾(Nudaurelia cytheria cytheria)幼虫的5种病毒的纯化,得到了生动的展示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
A rapid method for the isolation of genomic DNA from Aspergillus fumigatus. Purification of chlorpromazine-sensitive GTPase from rat cerebral cortex. Evaluation of a purification procedure for the muscarinic receptor for the purpose of quantitative receptor assays of anticholinergics. Part A: The membrane-bound receptor. Evaluation of a purification procedure for the muscarinic receptor for the purpose of quantitative receptor assays of anticholinergics. Part B: The solubilized receptor. Purification and characterization of rat parotid glycosylated, basic and acidic proline-rich proteins.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1