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肝胆相照论坛 论坛 学术讨论& HBV English 高纯度逆转录酶结构域的筛选和评估抗乙肝病毒聚合酶的新 ...
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高纯度逆转录酶结构域的筛选和评估抗乙肝病毒聚合酶的新 [复制链接]

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发表于 2020-8-7 11:02 |只看该作者 |倒序浏览 |打印
Screening and Evaluation of Novel Compounds against Hepatitis B Virus Polymerase Using Highly Purified Reverse Transcriptase Domain
Eriko Ohsaki  1 , Keiji Ueda  1
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    Division of Virology, Department of Microbiology and Immunology, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, Suita, Osaka 565-0871, Japan.

    PMID: 32752057 DOI: 10.3390/v12080840

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Abstract

Hepatitis B virus (HBV) polymerase seems to be very hard to express and purify sufficiently, which has long hampered the generation of anti-HBV drugs based on the nature of the polymerase. To date, there has been no useful system developed for drug screening against HBV polymerase. In this study, we successfully obtained a highly purified reverse transcriptase (RT) domain of the polymerase, which has a template/primer and substrate binding activity, and established a novel high-throughput screening (HTS) system using purified RT protein for finding novel polymerase inhibitors. To examine whether the assay system provides reliable results, we tested the small scale screening using pharmacologically active compounds. As a result, the pilot screening identified already-known anti-viral polymerase agents. Then, we screened 20,000 chemical compounds and newly identified four hits. Several of these compounds inhibited not only the HBV RT substrate and/ template/primer binding activity, but also Moloney murine leukemia virus RT activity, which has an elongation activity. Finally, these candidates did show to be effective even in the cell-based assay. Our screening system provides a useful tool for searching candidate inhibitors against HBV.

Keywords: hepatitis B virus; high-throughput screening; polymerase; reverse transcriptase.

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发表于 2020-8-7 11:02 |只看该作者
高纯度逆转录酶结构域的筛选和评估抗乙肝病毒聚合酶的新型化合物
大崎绘里子1,上田敬司1
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    大阪大学医学研究生院微生物学和免疫学系病毒学教研室,大阪府吹田市山田冈2-2-2,日本大阪565-0871。

    PMID:32752057 DOI:10.3390 / v12080840

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抽象

乙型肝炎病毒(HBV)聚合酶似乎很难表达和纯化,这很长一段时间以来一直阻碍了基于聚合酶性质的抗HBV药物的产生。迄今为止,还没有开发出可用于针对HBV聚合酶进行药物筛选的有用系统。在这项研究中,我们成功获得了具有模板/引物和底物结合活性的聚合酶的高纯度逆转录酶(RT)域,并使用纯化的RT蛋白建立了新颖的高通量筛选(HTS)系统,以寻找新的聚合酶抑制剂。为了检查测定系统是否提供可靠的结果,我们测试了使用药理活性化合物进行的小规模筛选。结果,初步筛选确定了已知的抗病毒聚合酶试剂。然后,我们筛选了20,000种化合物,并新发现了4个匹配项。这些化合物中的几种不仅抑制HBV RT底物和/模板/引物结合活性,而且抑制莫洛尼鼠白血病病毒RT活性,后者具有延伸活性。最后,这些候选物的确显示出了即使在基于细胞的测定中也是有效的。我们的筛选系统为寻找候选抗HBV抑制剂提供了有用的工具。

关键词:乙型肝炎病毒;高通量筛选聚合酶逆转录酶。

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发表于 2020-8-7 11:04 |只看该作者
StephenW 发表于 2020-8-7 11:02
高纯度逆转录酶结构域的筛选和评估抗乙肝病毒聚合酶的新型化合物
大崎绘里子1,上田敬司1
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发表于 2020-8-7 11:56 |只看该作者
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