陈明周教授,博士生导师

学科专业

研究方向

实验室位置

9001cc金沙大楼4015室

联系电话

027-68756816

Email

chenmz@whu.edu.cn

教育及工作经历

1992-1996:华中农业大学,土壤与植物营养专业,学士

1996-2002:华中农业大学,微生物学专业,博士

2002-2005:法国里昂第一大学感染与免疫学系,博士后

2005-2009:美国克利夫兰临床医院,分子遗传学系,博士后

2009-至今:9001cc金沙,病毒学国家重点实验室,教授


主要学术兼职

《Journal of Virology》编委 (Editorial Board Member)

《Frontiers in Cellular and Infection Microbiology》副主编 (Associate Editor)

《Virologica Sinica》编委 (Editorial Board Member)

美国微生物学会会员

美国病毒学会会员

中国微生物学会会员

中国微生物学会病毒学青年专业委员会委员

湖北生物工程学会常务理事


奖励及荣誉

2018年:国家杰出青年科学基金获得者(医学部)

2017年:9001cc金沙以诚为本珞珈学者特聘教授

2014年:教育部新世纪优秀人才支持计划获得者

2014年:湖北省杰出青年基金获得者


研究方向概述

我们长期致力于呼吸道病毒和肠道病毒复制、感染与致病机制研究及新型疫苗研发,综合运用包括病毒学、细胞生物学和活细胞荧光技术在内的多学科实验系统,解析病毒在宿主细胞内复制、组装、释放及病毒与宿主细胞的相互作用过程,同时也探讨病毒诱导并逃逸/劫持细胞的抗病毒反应(如自噬和应激颗粒反应等)过程,为阐明病毒感染和致病的分子机制及鉴定有效抗病毒药物靶点奠定了基础。经过近十年的发展,我们已取得了一系列原创性、系统性成果。包括:1)系统阐明了病毒聚合酶和核心蛋白相互作用能够形成一种特殊的结构-包涵体,它担负病毒RNA合成的新功能;2)深入研究了病毒基质蛋白调节病毒粒子组装和释放的新机制;3)发现病毒基质蛋白和聚合酶协同调节/劫持细胞自噬过程,从而最大限度增强病毒的复制和感染能力;4)解析了病毒逃逸宿主细胞应激颗粒抗病毒反应的分子机制,提出弱化病毒复制和感染的新策略。


主持课题项目

1. 国家杰出青年科学基金项目(医学部)(基金号:81825015)2019-2023(主持),400万

2. 国家自然科学基金重点项目(基金号:31630086)2017-2021(主持),345万

3. 国家自然科学基金面上项目(基金号:81471939)2015-2018(主持),100万

4. 国家自然科学基金面上项目(基金号:81271816)2013-2016(主持),70万

5. 国家重点研发计划重点专项(基金号:2017YFA0505800)2017-2022(骨干),130万

6. 国家科技重大专项“艾滋病和病毒性肝炎等重大传染病防治”(基金号:2018ZX10101004) 2018-2020 (骨干),114万

7. 教育部新世纪优秀人才支持计划 2014-2016(主持),50万

8. 湖北省自然科学基金创新群体(基金号:2017CFA022)2017-2019(主持),50万

9. 湖北省杰出青年基金 2014-2016(主持),10万


代表性论文(*为通讯作者)

1) Li Z, Guo D, Qin Y*,Chen M*. PI4KB on inclusion bodies formed by ER membrane remodeling facilitates replication of human parainfluenza virus type 3.Cell Reports. Nov 19; 29(8):2229-2242

2) Zhang Q#, Sharma N#, Zheng Z*,Chen M*. Viral Regulation of RNA Granules in Infected Cells.Virol Sin. 2019 Apr;34(2):175-191.

3) Tang Q, Liu P,Chen M*, Qin Y*. 2019. Virion-Associated Cholesterol Regulates the Infection of Human Parainfluenza Virus Type 3.Viruses. May 15;11(5).

4) Yang X, Hu Z, Zhang Q, Fan S, Zhong Y, Guo D, Qin Y,Chen M*.2019. SG formation relies on eIF4GI-G3BP interaction which is targeted by picornavirus stress antagonists.Cell Discov. eCollection.

5) Zhang L, Qin Y,Chen M*.2018. Viral strategies for triggering and manipulating mitophagy.Autophagy. 14(10):1665-1673.

6) Zhang S#, Cheng Q#, Luo C, Qin Y*,Chen M*.2018. Human Parainfluenza Virus Type 3 Matrix Protein Reduces Viral RNA Synthesis of HPIV3 by Regulating Inclusion Body Formation.Viruses. 11;10(3).

7) Hu Z, Wang Y, Tang Q, Yang X, Qin Y,Chen M*.2018. Inclusion bodies of human parainfluenza virus type 3 inhibit antiviral stress granule formation by shielding viral RNAs.PLoS Pathog14(3): e1006948.

8) Yang X, Hu Z, Fan S, Zhang Q, Zhong Y, Guo D, Qin Y,Chen M*.2018Picornavirus 2A protease regulates stress granule formation to facilitate viral translation.PLoS Pathog14(2): e1006901. https://doi.org/10.1371/journal.ppat.1006901.

9) Zhang S#, Cheng Q#, Luo C, Yin L, Qin Y*,Chen M*.2018. An alanine residue in human parainfluenza virus type 3 phosphoprotein is critical for restricting excessive N0-P interaction and maintaining N solubility.Virology. 518:64-76.

10) Ding B#, Zhang L#, Li Z, Zhong Y, Tang Q, Qin Y,Chen M*. 2017. The Matrix Protein of Human Parainfluenza Virus Type 3 Induces Mitophagy that Suppresses Interferon Responses.Cell Host Microbe. 21(4):538-547.

11) Zhang S#, Jiang Y#, Cheng Q, Zhong Y, Qin Y,Chen M*. 2017. Inclusion body fusion of human parainfluenza virus type 3 regulated by acetylated α-tubulin enhances viral replication.Journal of Virology. 91(3). pii: e01802-16.

12) Jiang Y, Qin Y*,Chen M*. 2016. Host-Pathogen Interactions in Measles Virus Replication and Anti-Viral Immunity.Viruses, 8 (11), E308 (Invited review).

13) Yan Q#, Wu L#, Chen L, Qin Y*, Pan Z*,Chen M*. 2016. Vesicular stomatitis virus-based vaccines expressing EV71 virus-like particles elicit strong immune responses and protect newborn mice from lethal challenges.Vaccine. 34:4196-4204.

14) Zhang G#, Zhong Y#, Qin Y,Chen M*. 2015. Interaction of Human Parainfluenza Virus Type 3 Nucleoprotein with Matrix Protein Mediates Internal Viral Protein Assembly.Journal of Virology. 90(5):2306-15.

15) Ding B, Qin Y,Chen M*. 2016. Nucleocapsid proteins: roles beyond viral RNA packaging.WIREs RNA. 7(2):213-26. (Invited review).

16) Chen L, Zhong Y, Hu Z, Qin Y. Chen M.Chen M*. 2016. Two second-site mutations compensate the engineered mutation of R7A in vesicular stomatitis virus nucleocapsid protein.Virus Research, 214:59-64.

17) Chen L#, Yan Q#, Lu G, Hu Z, Zhang G, Zhang S, Ding B, Jiang Y, Zhong Y, Gong P,Chen M*. 2015. Several residues within the N-terminal arm of vesicular stomatitis virus nucleoprotein play a critical role in protecting viral RNA from nuclease digestion.Virology.478:9-17.

18) Ding B, Zhang G, Yang X, Zhang S, Chen L, Yan Q, Xu M, Banerjee AK,Chen M*. 2014. Phosphoprotein of human parainfluenza virus type 3 blocks autophagosome-lysosome fusion to increase virus production.Cell Host & Microbe.15(5):564-77.

19) Zhang G, Zhang S, Ding B, Yang X, Chen L, Yan Q, Jiang Y, Zhong Y,Chen M*. 2014. A Leucine Residue in C-terminus of Human Parainfluenza Virus Type 3 Matrix Protein Is Essential for Efficient Virus-Like Particle and Virion Release.Journal of Virology. 88(22):13173-88.

20) Zhang S, Chen L, Zhang G, Yan Q, Yang X, Ding B, Tang Q, Sun S, Hu Z,Chen M*. 2013. An amino acid of human parainfluenza virus type 3 nucleoprotein is critical for template function and cytoplasmic inclusion body formation.Journal of Virology. 87(22):12457-70.

21) Chen L, Zhang S, Banerjee AK andChen M*. 2013. N-Terminal Phosphorylation of Phosphoprotein of Vesicular Stomatitis Virus Is Required for Preventing Nucleoprotein from Binding to Cellular RNAs and for Functional Template Formation.Journal of Virology. 87(6):3177-86.

22)Chen M, Ogino T, Banerjee AK*.2007. Interaction of vesicular stomatitis virus P and N proteins: Identification of two overlapping domains at the N-terminus of P that are involved in N0-P complex formation and encapsidation of viral genome RNA.Journal of Virology. 81(24):13478-85.

23)Chen M, Ogino T, Banerjee AK*.2006. Mapping and functional role of the self-association domain of vesicular stomatitis virus phosphoprotein.Journal of Virology. 80(19): 9511-8.

24)Chen Mand Gerlier D*.2006.Viral Hijacking of Cellular Ubiquitination Pathways as an Anti-Innate Immunity Strategy.Viral Immunology. 19(3): 349-362.

25)Chen M, Cortay JC, Logan IR, Sapountzi V, Robson CN, Gerlier D*.2005. Inhibition of ubiquitination and stabilization of human ubiquitin E3 ligase PIRH2 by measles virus phosphoprotein.Journal of Virology. 79(18): 11824-36.

职称 教授,博士生导师 实验室地址 9001cc金沙大楼4015室
联系电话 027-68756816 Email chenmz@whu.edu.cn
入选时间 2018 学科专业
研究方向

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