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新型登革病毒RNA聚合酶小分子抑制剂Z1降低登革病毒复制和感染的研究

郭颂欣 何士俊 黄翠红 姚新刚 刘叔文

中国药理学通报2018,Vol.34Issue(6):790-796,7.
中国药理学通报2018,Vol.34Issue(6):790-796,7.DOI:10.3969/j.issn.1001-1978.2018.06.011

新型登革病毒RNA聚合酶小分子抑制剂Z1降低登革病毒复制和感染的研究

Z1, a novel DENV2 NS5 RdRp small molecular inhibitor, inhibits DENV2 replication and infection

郭颂欣 1何士俊 1黄翠红 1姚新刚 1刘叔文1

作者信息

  • 1. 南方医科大学药学院,广东省新药筛选重点实验室,广州市新发病毒防治药物研究重点实验室,广东 广州 510515
  • 折叠

摘要

Abstract

Aim To screen novel NS5 inhibitors a-gainst dengue virus ( DENV) replication. Methods His-tagged DENV2 NS5 RNA-dependent polymerase ( NS5 RdRp ) was expressed and purified in BL21 cells. The binding ability of the small molecules to NS5 polymerase was determined by SPR assay. The activity of dengue inhibition by Z1 was determined by CPE, LDH and plaque assay. RNA synthesis was as-sessed by Real-time PCR. The dsRNA synthesis and viral proteins were detected by immunofluorescence as-say. The level of viral proteins was examined by West-ern blot. The stage of DENV life cycle was evaluated by time of drug-addition assay. Results A small mo-lecular Z1 was discovered, which could bind to NS5 RdRp. Z1 inhibited DENV2 RNA replication, synthe-sis of dsRNA and protein synthesis in post-entry stage of dengue life-cycle. Cell based assay confirmed that Z1 inhibited DENV-induced cell death with EC50 val-ues of 4. 75μmol·L-1 . Conclusions The novel NS5 inhibitor Z1, inhibits DENV2 RNA replication, protein synthesis and release of progeny virus, which may be severed as an anti-DENV2 antiviral drug for further de-velopment.

关键词

NS5RdRp抑制剂/登革病毒RNA聚合酶/2型登革病毒/抗病毒药物/SPR/病毒复制

Key words

NS5 RdRp inhibitors/DENV RNA poly-merase/DENV2 infection/antiviral drugs/SPR/virus replication

分类

医药卫生

引用本文复制引用

郭颂欣,何士俊,黄翠红,姚新刚,刘叔文..新型登革病毒RNA聚合酶小分子抑制剂Z1降低登革病毒复制和感染的研究[J].中国药理学通报,2018,34(6):790-796,7.

基金项目

国家自然科学基金资助项目( No 81603118 ) ( No 81603118 )

广东省医学科学技术研究基金( No A2016119 ) ( No A2016119 )

南方医科大学科研助手项目 (No C1032242) (No C1032242)

国家自然科学基金-广东联合基金重点项目(K1060014) (K1060014)

中国药理学通报

OA北大核心CSCDCSTPCD

1001-1978

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