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{"title":"AAV Production Everywhere: A Simple, Fast, and Reliable Protocol for In-house AAV Vector Production Based on Chloroform Extraction.","authors":"Matilde Negrini, Gang Wang, Andreas Heuer, Tomas Björklund, Marcus Davidsson","doi":"10.1002/cpns.103","DOIUrl":null,"url":null,"abstract":"<p><p>Recombinant adeno-associated virus (rAAV) is a mammalian virus that has been altered to be used as a gene delivery vehicle. Several changes to the viral genome have made them replication deficient so that this aspect of the viral infection cycle is under full control of the experimenter, while maintaining gene expression machinery. Over the last decades, rAAVs have become the gold standard for studying in vivo gene function and are especially favorable for gene transfer in the central nervous system. AAVs have been proven safe and provide stable gene expression over a long period of time. They are extensively used in preclinical experiments and show great potential for clinical applications. However, the use of AAVs in preclinical settings are often held back due to availability. Waiting lines are long at commercial production facilities, and in-lab production is hindered due to lack of specific laboratory equipment needed. Here we present a novel production method that can be carried out in any molecular biology laboratory using standard laboratory equipment. We provide a simple, fast, and streamlined protocol for production that can result in titers comparable with the more time-consuming iodixanol gradient ultracentrifugation method. The yield using this protocol is high enough for any type of study where AAV is the vector of choice. © 2020 The Authors.</p>","PeriodicalId":40016,"journal":{"name":"Current Protocols in Neuroscience","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2020-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpns.103","citationCount":"26","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Neuroscience","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/cpns.103","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Neuroscience","Score":null,"Total":0}
引用次数: 26
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Abstract
Recombinant adeno-associated virus (rAAV) is a mammalian virus that has been altered to be used as a gene delivery vehicle. Several changes to the viral genome have made them replication deficient so that this aspect of the viral infection cycle is under full control of the experimenter, while maintaining gene expression machinery. Over the last decades, rAAVs have become the gold standard for studying in vivo gene function and are especially favorable for gene transfer in the central nervous system. AAVs have been proven safe and provide stable gene expression over a long period of time. They are extensively used in preclinical experiments and show great potential for clinical applications. However, the use of AAVs in preclinical settings are often held back due to availability. Waiting lines are long at commercial production facilities, and in-lab production is hindered due to lack of specific laboratory equipment needed. Here we present a novel production method that can be carried out in any molecular biology laboratory using standard laboratory equipment. We provide a simple, fast, and streamlined protocol for production that can result in titers comparable with the more time-consuming iodixanol gradient ultracentrifugation method. The yield using this protocol is high enough for any type of study where AAV is the vector of choice. © 2020 The Authors.
AAV生产无处不在:基于氯仿提取的内部AAV载体生产的简单,快速和可靠的协议。
重组腺相关病毒(rAAV)是一种哺乳动物病毒,已被改造为基因传递载体。病毒基因组的一些变化使其复制缺陷,因此病毒感染周期的这一方面在实验者的完全控制下,同时保持基因表达机制。在过去的几十年里,raav已经成为研究体内基因功能的金标准,尤其有利于中枢神经系统的基因转移。aav已被证明是安全的,并在很长一段时间内提供稳定的基因表达。它们广泛用于临床前实验,具有很大的临床应用潜力。然而,由于可用性的原因,在临床前环境中使用aav往往受到阻碍。商业生产设施的等待队伍很长,由于缺乏所需的特定实验室设备,实验室内的生产受到阻碍。在这里,我们提出了一种新的生产方法,可以在任何分子生物学实验室使用标准实验室设备进行。我们提供了一种简单、快速和流线型的生产方案,可以产生与更耗时的碘二醇梯度超离心方法相当的滴度。对于选择AAV作为载体的任何类型的研究,使用该方案的产量都足够高。©2020作者。
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