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一种新型下一代测序和分析平台,用于评估从病毒 DNA 提取物中鉴定重组腺相关病毒制剂的身份。

A Novel Next-Generation Sequencing and Analysis Platform to Assess the Identity of Recombinant Adeno-Associated Viral Preparations from Viral DNA Extracts.

机构信息

Addgene, Watertown, Massachusetts, USA.

出版信息

Hum Gene Ther. 2020 Jun;31(11-12):664-678. doi: 10.1089/hum.2019.277. Epub 2020 Apr 15.

Abstract

Recombinant adeno-associated virus (rAAV) vectors are increasingly popular gene delivery tools in biological systems. They are safe and lead to high-level, long-term transgene expression. rAAV are available in multiple serotypes, natural or engineered, which enable targeting to a wide array of tissues and cell types. In addition, rAAVs are relatively easily produced in a well-equipped lab or obtained from a viral vector core facility. Unfortunately, there is no standardization of quality control assays beyond titering and purity assessments. Next-generation sequencing (NGS) can be used to identify rAAV preparations. Because the rAAV genome is single stranded, previous studies have assumed that rAAV genomes must be converted to double strands before NGS. We demonstrate that rAAV DNA extracts exist primarily as double-stranded species. We hypothesize that these molecules form from the natural base pairing of complementary [+] and [-] strands after DNA extraction and show that rAAV DNA extracts are sufficient templates for downstream NGS without the labor-intensive double-stranding step. Here, we provide a detailed protocol for the simple and rapid NGS of rAAV genomes from DNA extracts. With this protocol, users can quickly confirm the identity of an rAAV preparation and detect the presence of contaminating rAAV DNA. In addition, we share custom Python scripts that allow users to accurately determine the serotype and detect Cre-independent DNA recombination events in rAAV containing Lox sites within minutes. We have used these scripts to analyze more than 100 rAAV preparations. Although we focused on the detection of cross-contaminating rAAV DNA and recombination events, our Python scripts can be customized to detect other sequences or events, such as reverse packaging of plasmid backbone or DNA from the packaging cell line. We find that the NGS of rAAV DNA extracts, termed viral genome sequencing, is a simple and powerful method for rAAV validation.

摘要

重组腺相关病毒 (rAAV) 载体在生物系统中越来越受欢迎,是基因传递工具。它们安全且可实现高水平、长期的转基因表达。rAAV 有多种血清型,包括天然或工程改造的血清型,可靶向多种组织和细胞类型。此外,rAAVs 相对容易在设备齐全的实验室中生产,或从病毒载体核心设施中获得。不幸的是,除了滴度和纯度评估外,没有 rAAV 质量控制检测的标准化。下一代测序 (NGS) 可用于鉴定 rAAV 制剂。由于 rAAV 基因组是单链的,因此之前的研究假设 rAAV 基因组在 NGS 之前必须转化为双链。我们证明 rAAV DNA 提取物主要以双链形式存在。我们假设这些分子是在 DNA 提取后由互补的 [+] 和 [-] 链的自然碱基配对形成的,并表明 rAAV DNA 提取物是下游 NGS 的充分模板,无需繁琐的双链形成步骤。在这里,我们提供了一种从 DNA 提取物中快速简便地对 rAAV 基因组进行 NGS 的详细方案。使用此方案,用户可以快速确认 rAAV 制剂的身份,并检测污染的 rAAV DNA 的存在。此外,我们还共享了自定义的 Python 脚本,允许用户在几分钟内准确确定 rAAV 的血清型,并检测含有 Lox 位点的 rAAV 中的 Cre 非依赖性 DNA 重组事件。我们已经使用这些脚本分析了 100 多个 rAAV 制剂。尽管我们专注于检测交叉污染的 rAAV DNA 和重组事件,但我们的 Python 脚本可以定制,以检测其他序列或事件,例如质粒骨架的反向包装或包装细胞系的 DNA。我们发现 rAAV DNA 提取物的 NGS,即病毒基因组测序,是一种简单而强大的 rAAV 验证方法。

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