School of Pharmaceutical Science and Technology
Associate professor
PhD Supervisor
Protein Engineering,Structure Biology, Drug Discovery
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Mei's group integrates techniques from molecular biology, cell biology, structure biology, protein engineering, and yeast genetics to conduct research centered on new drug development. The group’s work focuses on three main areas:
Discovery of novel drug targets:
By leveraging cell biology and structural biology approaches, we investigate the function and regulatory mechanisms of potential disease-related targets, aiming to identify new drug targets and novel druggable sites.Development of biologic macromolecule-based drugs:
We have established a comprehensive nanobody development platform, which is employed to design innovative targeted therapeutics against key disease-related targets.Biosynthesis of natural product-based drugs and drug precursors:
Using structural biology and protein engineering, we conduct rational engineering of key biosynthetic enzymes involved in the production of important natural products, improving their catalytic efficiency and stability. These optimized enzymes are then integrated into microbial cell factories such as yeast to enhance the biosynthetic efficiency of the target compounds.
- Papers
- [1] Structural Insights into the Substrate Recognition of Ginsenoside Glycosyltransferase Pq3-O-UGT2
- [2] Structure-function and engineering of plant UDP-glycosyltransferase
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- [3] Rpl12 is a conserved ribophagy receptor
- [4] Structural Basis of the LARP4-Filamin A Interaction and Competition with Integrin β7 Tails
- [5] TGM1/3-mediated transamidation of Exo70 promotes tumor metastasis upon LKB1 inactivation
- [6] Engineering of triterpene metabolism and overexpression of the lignin biosynthesis gene PAL promotes ginsenoside Rg3 accumulation in ginseng plant chassis
- [7] Inducing enhanced neutralizing antibodies against broad SARS-CoV-2 variants through glycan-shielding multiple non-neutralizing epitopes of RBD
- [8] Yeast Genome Mutagenesis with Multi-Mismatch PCR: A Rapid and Efficient Strategy for Site-Directed Mutagenesis in Saccharomyces cerevisiae
- [9] Highly efficient overexpression and purification of multisubunit tethering complexes in Saccharomyces cerevisiae
- [10] Expression, purification, characterization and crystallization of Panax quinquefolius ginsenoside glycosyltransferase Pq3-O-UGT2
- [11] Single-Molecule Electrical Profiling of Peptides and Proteins
- [12] Characterization of dsRNA binding proteins through solubility analysis identifies ZNF385A as a dsRNA homeostasis regulator
- [13] Acetylation of SCFD1 regulates SNARE complex formation and autophagosome-lysosome fusion
- [14] mTOR-mediated phosphorylation of VAMP8 and SCFD1 regulates autophagosome maturation
- [15] The exocyst complex
- [16] Cryo-EM structure of the exocyst complex
- Honors & Awards
- [1] 入选天津市青年人才项目
- [2] 入选天津市青年人才托举工程





