Demin Zhou
周德敏
Senior Principal Investigator
deminzhou@bjmu.edu.cn
Home page of research group:http://sklnbd.bjmu.edu.cn/k/e/action/ListInfo/?classid=19
Timeline
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2021 - Present
Shenzhen Bay Laboratory Senior Principal Investigator
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2008 - Present
Peking University Professor
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2003.05 - 2008.08
Immusol, USA Director of Drug Discovery
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2002.04 - 2003.04
Roche Chugai, USA Senior Researcher
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1999.01 - 2002.03
University of California, Berkeley Postdoc
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1996.07 - 1998.12
University of Tsukuba, Japan Assistant Professor
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1992.09 - 1996.07
Beijing Medical University PhD
Research Areas
Research on new technologies and methods in drug research and development
Development and research of novel antiviral small molecules
Development and modification of protein biomacromolecule drugs
Discovery and confirmation of drug targets /biomarkers
Development of new influenza vaccine (PTC vaccine)
Development and research of natural drugs, bionic drugs and biological candidate drugs
Highlights
Education & work highlight experience:
1.He is the editorial board member of J Med Chem and Eur J Med Chem, and executive editor of J. chin. Pharm. SCI.
2. As Dean of School of pharmacy and professor of Department of chemical biology of Peking University, he has trained a large number of professionals.
3. He has successively won the following Honors: chief scientist of the major state basic research development program(973 program) of china (2010), Changjiang Scholar of the Ministry of Education (2013), leading scientist of national biological candidate drugs (2013), outstanding achievement award of 2017 WuXi App Tec Life Chemistry Research Award, and scientific and technological innovation leader of ‘ten thousand talents plan’ (2018)
4. In December 2016, the breakthrough progress of Demin Zhou / Lihe Zhang research team was published in Science (DOI: 10.1126/ science.aah5869 ). Taking the influenza virus as a model, the researchers invented the technology of artificially controlling virus replication so as to directly transform the virus into a vaccine. That is to say, in the case of retaining the complete structure and infectivity of the virus, only one triplet of the virus genome is mutated, so that the influenza virus changes from a lethal infectious source to a preventive vaccine, and then mutates more than three triplets, and the virus changes from a preventive vaccine to a drug for treating virus infection, and the efficacy increases with the increase of triplet number. This technology not only makes vaccine research and development no longer complex, but also gets rid of the dependence on the knowledge of virus biology, and is suitable for almost all viruses. This discovery overturned the concept of virus vaccine research and development, and made a major breakthrough in live virus vaccine. The achievement was awarded as "top ten scientific advances in China" and "annual paper of International Society of vaccines"
Key projects undertaken:
1. National Natural Science Foundation of China, innovative research group, 81821004, biopharmaceutical innovation based on precise modification of endogenous macromolecules, (2019.1-2023.12), 10.5 million yuan, in research, presided over
2. National Natural Science Foundation of China, major research program, 91753202, virus-cell fusion research and chemical intervention, target discovery and transformation based on spatiotemporal dynamic modification of virus envelope protein, (2018.1-2021.12), 3 million yuan, under research and presided over
3. National Natural Science Foundation of China, key project, 81530090, Study on the relationship between the structural basis, delivery targeting and immunogen adverse reactions of recombinant viral vector based on site directed modification of membrane protein, (2016.1- 2020.12), 2.74 million yuan, conclusion (excellent), chair
Taking the influenza virus as a model, researchers invented the technology of artificially controlling virus replication so as to directly transform the virus into a vaccine. That is, in the case of retaining the complete structure and infectivity of the virus, only one triplet of the virus genome is mutated to change the influenza virus from a lethal infectious source to a preventive vaccine, and then more than three triplets are mutated to change the virus from a preventive vaccine to a vaccine which is a drug for the treatment of viral infection, and its efficacy increases with the increase of triplet number. This technology not only makes vaccine research and development no longer complex, but also gets rid of the dependence on the knowledge of virus biology, and is suitable for almost all viruses.
Honors
1999 The first national excellent doctoral dissertation winner
2010 Chief Scientist of the major state basic research development program(973 program)
2013 Changjiang Scholars of the Ministry of Education
2013 National leading scientist of biological candidate drugs
2017 Ten Advances in Science in China
2017 International Vaccine Association annual paper winner
2017 Outstanding achievement award of WuXi App Tec Life Chemistry Research Award
Related News
People. CN | 将病毒直接转化为活疫苗及治疗性药物
http://scitech.people.com.cn/n1/2018/0227/c1007-29837856-2.html
Selected Publications
1. Zhang B#; Wang Y#; Yuan Y#; Sun J; Liu L; Huang D; Hu J; Wang M; Li S;Song W; Chen H; Zhou D*; Zhang X*; In vitro elimination of autoreactive B cells from rheumatoid arthritis patients by universal Car-T cells redirected by citrulline-bearing peptide epitopes, Annals of the Rheumatic Diseases, 2020, 80(2): 176-184.
2. Wang, Y; Li, S; Tian, Z; Sun, J; Liang, S; Zhang, B; Bai, L; Zhang, Y;Zhou, X; Xiao, S; Zhang, Q; Zhang, L; Zhang, C*; Zhou D*; Generation of a caged lentiviral vector through an unnatural amino acid for photo-switchable transduction , Nucleic Acids Research, 2019, 47(19): E114-+.
3. Si L; Meng K; Tian Z; Sun J; Li H; Zhang Z; S Veronica; Li H; Fu G; Xia Q; Xiao S; Zhang L; Zhou D*; Triterpenoids manipulate a broad range of virus-host fusion via wrapping the HR2 domain prevalent in viral envelopes , Science Advances, 2018, 4(11): 0-eaau8408.
4. Wu L#; Chen J#; Wu Y#; Zhang B; Cai X; Zhang Z; Wang Y; Si L; Xu H;Zheng Y; Zhang C; Liang C; Li J; Zhang L; Zhang Q; Zhou D*; Precise and combinatorial PEGylation generates a low-immunogenic and stable form of human growth hormone , Journal of Controlled Release, 2017, 249: 84-93.
5. Si L#; Xu H#; Zhou X; Zhang Z; Tian Z; Wang Y; Wu Y; Zhang B; Niu Z;Zhang C; Fu G; Xiao S; Xia Q; Zhang L; Zhou D*; Generation of influenza A viruses as live but replication-incompetent virus vaccines. , Science, 2016, 354(6316): 1170-1173.
6. Ji, D., Zhang, Y., Sun, J., Zhang, B., Ma, W., Cheng, B., Wang, X., Li, Y., Mu, Y., Xu, H., Wang, Q., Zhang, C., Xiao, S., Zhang, L., & Zhou, D.* (2024). An engineered influenza virus to deliver antigens for lung cancer vaccination. Nature biotechnology, 42(3), 518–528.
7. Zhang B, Sun J, Wang Y, Ji D, Yuan Y, Li S, Sun Y, Hou Y, Li P, Zhao L, Yu F, Ma W, Cheng B, Wu L, Hu J, Wang M, Song W, Li X, Li H, Fei Y, Chen H, Zhang L, Tsokos GC, Zhou D*, Zhang X. (2021). Site-specific PEGylation of interleukin-2 enhances immunosuppression via the sustained activation of regulatory T cells. Nature biomedical engineering, 5(11), 1288–1305.
8. Si, L., Xu, H., Zhou, X., Zhang, Z., Tian, Z., Wang, Y., Wu, Y., Zhang, B., Niu, Z., Zhang, C., Fu, G., Xiao, S., Xia, Q., Zhang, L., & Zhou, D*. (2016). Generation of influenza A viruses as live but replication-incompetent virus vaccines. Science (New York, N.Y.), 354(6316), 1170–1173.