Current Location : Home > Faculty > All PIs > GUO YU > Content

郭宇 研究员 GUO YU
Ph.D., Professor, State laboratory of Chemical Medical Biology, graduated from Nankai University, visiting scholar of Stanford University (2017-2018)
Special Talent:
Address: No. 38 Tongyan Road, Jinnan District, Tianjin
Telephone:
Email: guoyu@nankai.edu.cn
Research Group Website: N/A

Education &Research History:

2020-Present Full Professor, College of Life Sciences, Nankai University.

2020-Present Principle investigator, State Key Laboratory of Medicinal Chemical Biology.

2017-2018 Visiting Scholar, Medical School, Stanford University.

2015-2020 Associate Professor, College of Pharmacy, Nankai University.

2012-2015 Lecturer, College of Pharmacy, Nankai University.

2010-2012 Ph.D., College of Life Sciences, Nankai University

2003-2007 B.A., College of Life Sciences, Nankai University.

Research Interest:

Yu's laboratory is broadly interested in the entry mechanism and host defense of viruses infection. Our principal goal is to exploit mechanistic and structural information on virus-host interactions, and provide innovative solutions to disease prevention and therapeutics. We develop structural and functional tools to study macro-molecular assemblies such as virus particle, virus-antibody complex and ligand-receptor complex, and combine both of experimental and computational approaches to address critical questions in virology and immunology research.

Honors and Awards:

2021 elected:The National "Ten Thousand Talents Program" for Young Outstanding Talents

2021 received: The Tianjin Youth Science and Technology Award

2020 elected:The China Association for Science and Technology's "Young Talent Nurturing Project."

Scientific Achievements & Selected Publications

1.   Guo Yu*, et.al, Rao Zihe*, Discovery and characterization of potent pan-variant SARS-CoV-2 neutralizing antibodies from individuals with Omicron breakthrough infection. Nature Communications, 2023, 14(1):3537.

2.   Guo Yu*, et.al, Rao Zihe*, A SARS-CoV-2 neutralizing antibody with extensive Spike binding coverage and modified for optimal therapeutic outcomes. Nature Communications, 2021, 12(1): 2623-2623.

3.   Fu Dan, et.al, Guo Yu*, Structural basis for SARS-CoV-2 neutralizing antibodies with novel binding epitopes. PLoS biology, 2021, 19(5) : e3001209-e3001209.

4.   Zhou Xingdong, et.al, Guo Yu*, Hongkai Zhang*, Xiaoming Yang*, Molecular deconvolution of the neutralizing antibodies induced by an inactivated SARS-CoV-2 virus vaccine. Protein & cell, 2021: 1-6.

5.   Li Guobang, et.al, Guo Yu*, Crystal structure of the African swine fever virus structural protein p35 reveals its role for core shell assembly. Protein & Cell, 2020, 11(8) : 600-605.

6.   Fu Dan, et.al, Guo Yu*, Structure of African swine fever virus p15 reveals its dual role for membrane-association and DNA binding. Protein & Cell, 2020, 11(8) : 606-612.

7.   Li Guobang, et.al, Guo Yu*, Crystal structure of the African swine fever virus pS273R protease and implications for inhibitor design. Journal of Virology, 2020, 94(10)

8.   Zhang Min, et.al, Guo Yu*, Design, Synthesis, and Evaluation of Novel Enterovirus 71 Inhibitors as Therapeutic Drug Leads for the Treatment of Human Hand, Foot and Mouth Disease. Journal of Medical Chemistry, 2020, 63(3) : 1233-1244.

9.   Li Guobang, et.al, Guo Yu*, Structural Insight into African Swine Fever Virus dUTPase Reveals a Novel Folding Pattern in the dUTPase Family. Journal of Virology, 2020, 94(4).