重组DNA
基因组
质粒
DNA测序
衣壳
DNA
生物
计算生物学
载体(分子生物学)
病毒学
病毒
腺相关病毒
基因
遗传学
作者
Émilie Lecomte,Adrien Léger,Magalie Penaud‐Budloo,Eduard Ayuso
出处
期刊:Methods in molecular biology
日期:2019-01-01
卷期号:: 85-106
被引量:10
标识
DOI:10.1007/978-1-4939-9139-6_5
摘要
With the success of clinical trials using recombinant adeno-associated viral vectors (rAAV), regulatory agencies ask for a more comprehensive characterization of process- and product- related impurities found in rAAV stocks in order to assess the potential risks for patients. During production, rAAV capsids are known to internalize illegitimate DNA fragments in addition to their recombinant genome. These contaminants can come from plasmid or helper virus DNA as well as from the producer host cell. Here, we describe a method based on high-throughput sequencing to identify and quantify residual DNA in rAAV vector lots. Contrary to qPCR, SSV-Seq (Single-Stranded DNA Virus Sequencing) offers a nonselective approach to determine the percentage of each DNA contaminant and analyze rAAV vector genome identity.
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