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腺相关病毒血清型 9 的陶瓷羟磷灰石层析法纯化及其分析。

Purification of Adeno-Associated Viral Vector Serotype 9 Using Ceramic Hydroxyapatite Chromatography and its Analysis.

机构信息

Division of Molecular and Medical Genetics, Center for Gene and Cell Therapy, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.

Chromatography Media Business Division, HOYA Technosurgical Corporation, Tokyo, Japan.

出版信息

Curr Protoc. 2024 Jun;4(6):e1068. doi: 10.1002/cpz1.1068.

Abstract

Adeno-associated virus (AAV) vectors can efficiently transduce exogenous genes into various tissues in vivo. Owing to their convenience, high efficiency, long-term stable gene expression, and minimal side effects, AAV vectors have become one of the gold standards for investigating gene functions in vivo, especially in non-clinical studies. However, challenges persist in efficiently preparing a substantial quantity of high-quality AAV vectors. Commercial AAV vectors are typically associated with high costs. Further, in-laboratory production is hindered by the lack of specific laboratory equipment, such as ultracentrifuges. Therefore, a simple, quick, and scalable preparation method for AAV vectors is needed for proof-of-concept experiments. Herein, we present an optimized method for producing and purifying high-quality AAV serotype 9 (AAV9) vectors using standard laboratory equipment and chromatography. Using ceramic hydroxyapatite as a mixed-mode chromatography medium can markedly increase the quality of purified AAV vectors. Basic Protocols and optional methods for evaluating purified AAV vectors are also described. © 2024 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Production of AAV9 vectors in 293EB cells Basic Protocol 2: Concentration and buffer exchange of AAV9 vectors from 293EB cell culture supernatants using tangential flow filtration Basic Protocol 3: Purification of AAV9 vectors from TFF samples using ceramic hydroxyapatite chromatography Basic Protocol 4: Analysis of the purified AAV9 vectors.

摘要

腺相关病毒(AAV)载体可以有效地将外源基因转导到体内的各种组织中。由于其方便、高效、长期稳定的基因表达和最小的副作用,AAV 载体已成为研究体内基因功能的黄金标准之一,尤其是在非临床研究中。然而,高效制备大量高质量 AAV 载体仍然存在挑战。商业 AAV 载体通常成本较高。此外,由于缺乏特定的实验室设备,如超速离心机,实验室生产也受到阻碍。因此,需要一种简单、快速和可扩展的 AAV 载体制备方法,用于验证概念实验。在此,我们使用标准实验室设备和色谱法,提出了一种优化的方法来生产和纯化高质量的 AAV 血清型 9(AAV9)载体。使用陶瓷羟基磷灰石作为混合模式色谱介质可以显著提高纯化 AAV 载体的质量。还描述了评估纯化 AAV 载体的基本方案和可选方法。

© 2024 作者。当前协议由 Wiley 期刊出版公司出版。

基本方案 1:在 293EB 细胞中生产 AAV9 载体

基本方案 2:使用切向流过滤从 293EB 细胞培养上清液中浓缩和交换 AAV9 载体的缓冲液

基本方案 3:使用陶瓷羟基磷灰石色谱法从 TFF 样品中纯化 AAV9 载体

基本方案 4:分析纯化的 AAV9 载体。

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