Yuchi Zhiguang
Yuchi Zhiguang
Doctor degree Professor

Zhiguang Yuchi, Ph.D., Professor, Institute of Elemento-organic Chemistry, graduated from McMaster University

Special Talent:Excellent Young Scientists Fund, NSFC

Address:4th Floor, Basic Science Center, Nankai University, Weijin Road #94, Tianjin, 300071, China

Telephone:

Email:yuchi@nankai.edu.cn

Research Group Website:https://www.yuchilab.com/

Research Interest:

1. Mechanistic Studies of Membrane Protein Targets
Investigating the structural basis of ligand recognition, allosteric regulation, gating, and species selectivity of membrane proteins, with a particular focus on ion channels.

2. AI-Driven Design of Small Molecules and Peptides
Integrating structural biology, artificial intelligence, and high-throughput screening to enable the rational design and optimization of bioactive small molecules and peptide therapeutics.

3. Discovery and Translation of Bioactive Molecules
Combining chemical synthesis, synthetic biology, and functional evaluation to develop bioactive molecules for next-generation green pesticides and innovative therapeutics. 
History:

1999-2003, BSc, School of Life Sciences, Fudan University, China

2003-2009, PhD, Department of Biochemistry and Biomedical Sciences, McMaster University, Canada

2009-2010, Postdoctoral Fellow, Cold Spring Harbor Laboratory, USA

2010-2016, Research Associate, Department of Biochemistry and Molecular Biology, University of British Columbia, Canada

2016-2021, Associate Professor, School of Pharmaceutical Science and Technology, Tianjin University, China

2021-2026, Professor/Vice Dean, School of Pharmaceutical Science and Technology, Tianjin University, China

2016-present, Adjunct Professor, Department of Biochemistry and Molecular Biology, University of British Columbia, Canada

2026-present, Professor, College of Chemistry, Nankai University, China

Honors and Awards

2013, Michael Smith Fellowship

2015, Michael John Page Award

2017, Excellence in Mentoring Award, American Chemical Society

2017, Young Thousand Talents Program, Tianjin

2020, Excellent Young Scientists Fund, National Natural Science Foundation of China

2023, Agricultural Chemistry Innovation Award, Chinese Chemical Society

2025, High-Level Natural Science Innovation Award, Tianjin University

2025, First Prize, Natural Science Award, the Ministry of Education of China
Scientific Achievements & Selected Publications

ResearcherID: N-5184-2016 | ORCID: 0000-0003-2595-9106

Selected Publications:

(1) Structural insights into insect-selective sodium channel toxins drive AI-enhanced biopesticide design, Nature Communications, 2026, 17(1): 3543.

(2) Crystal structures of ryanodine receptor reveal dantrolene and azumolene interactions guiding inhibitor development, Nature Communications, 2025, 16(1): 10110.

(3) AI-driven de novo enzyme design: Strategies, applications, and future prospects. Biotechnology Advances, 2025, 82:108603.

(4) Cryo-EM structures of ryanodine receptors and diamide insecticides reveal the mechanisms of selectivity and resistance, Nature Communications, 2024, 15(1): 9056.

(5) Structural basis for directional chitin biosynthesis. Nature, 2022, 610: 402-408.

(6) Structures of PKA–phospholamban complexes reveal a mechanism of familial dilated cardiomyopathy, eLife, 2022, 11(1): 1- 21.

(7) Anaerobic hydroxyproline degradation involving C–N cleavage by a glycyl radical enzyme, Journal of the American Chemical Society, 2022, 144(22): 9715-9722.

(8) The Glycyl Radical Enzyme Arylacetate Decarboxylase from Olsenella scatoligenes. ACS Catalysis, 2021, 11, 9: 5789–5794.

(9) Structural basis for diamide modulation of ryanodine receptor, Nature Chemical Biology, 2020, 16(1): 1246-1254.

(10) Two radical-dependent mechanisms for anaerobic degradation of the globally abundant organosulfur compound dihydroxypropanesulfonate, Proc. Nati. Acad. Sci., 2020, 117(27): 15599-15608.

(11) Variation among 532 genomes unveils the origin and evolutionary history of a global insect herbivore. Nature Communications, 2020, 11: 2321.

(12) Radical-mediated C-S bond cleavage in C2 sulfonate degradation by anaerobic bacteria, Nature Communications, 2019, 10(1): 1609.

(13) Crystal structure of diamondback moth ryanodine receptor Repeat34 domain reveals insect-specific phosphorylation sites. BMC Biology, 2019, 17: 77.

(14) Crystal structures of Ryanodine Receptor SPRY1 and tandem-repeat domains reveal a critical FKBP12 binding determinant. Nature Communications, 2015, 6:7947.

Professional Cultivation

Trained 6 Ph.D. students, 22 master’s students, and 3 postdoctoral fellows.