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AAV Production Everywhere: A Simple, Fast, and Reliable Protocol for In‐house AAV Vector Production Based on Chloroform Extraction

腺相关病毒 生物 病毒载体 载体(分子生物学) 计算生物学 遗传增强 基因传递 协议(科学) 计算机科学 基因 重组DNA 遗传学 医学 病理 替代医学
作者
Matilde Negrini,Gang Wang,Andreas Heuer,Tomas Björklund,Marcus Davidsson
出处
期刊:Current protocols in neuroscience [Wiley]
卷期号:93 (1): e103-e103 被引量:65
标识
DOI:10.1002/cpns.103
摘要

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.
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