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利用 MNase-qPCR 和高通量测序分析 HBV cccDNA 微染色体的可及性。

Analysis of HBV cccDNA Minichromosome Accessibility by MNase-qPCR and High-Throughput Sequencing.

机构信息

Key Laboratory of Medical Molecular Virology (MOE & NHC), Research Unit of Cure of Chronic Hepatitis B Virus Infection (CAMS), Shanghai Frontiers Science Center of Pathogenic Microorganisms and Infection, School of Basic Medical Sciences, Shanghai Medical College, Fudan University, Shanghai, China.

出版信息

Methods Mol Biol. 2024;2837:33-43. doi: 10.1007/978-1-0716-4027-2_4.

Abstract

The covalently closed circular DNA (cccDNA) of the hepatitis B virus (HBV) is organized as a minichromosome structure in the nucleus of infected hepatocytes and considered the major obstacle to the discovery of a cure for HBV. Until now, no strategies directly targeting cccDNA have been advanced to clinical stages as much is unknown about the accessibility and activity regulation of the cccDNA minichromosome. We have described the method for evaluation of the cccDNA minichromosome accessibility using micrococcal nuclease-quantitative polymerase chain reaction and high-throughput sequencing, which could be useful tools for cccDNA research and HBV cure studies.

摘要

乙型肝炎病毒(HBV)的共价闭合环状 DNA(cccDNA)在感染的肝细胞的细胞核中以微染色体结构存在,被认为是发现乙型肝炎病毒治愈方法的主要障碍。到目前为止,还没有直接针对 cccDNA 的策略被推进到临床阶段,因为对于 cccDNA 微染色体的可及性和活性调节知之甚少。我们描述了使用微球菌核酸酶-定量聚合酶链反应和高通量测序评估 cccDNA 微染色体可及性的方法,这可能是 cccDNA 研究和 HBV 治愈研究的有用工具。

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