Faculty
SELF-INTRODUCTION：
Dr. Jun Xu, Associate Professor at the School of Medicine, Southern University of Science and Technology (SUSTech), and Doctoral Supervisor. He has been selected for national and Guangdong provincial overseas high-caliber youth talent programs. xk星空官方网站 2014, he graduated with a bachelor's degree xk星空官方网站 Biotechnology from Huazhong University of Science and Technology. xk星空官方网站 2019, he obtained his Ph.D. xk星空官方网站 Basic Medical Sciences from the School of Medicine, Tsinghua University. Subsequently, he served as a visiting scholar and postdoctoral researcher at the Kobilka Institute of Innovative Drug Discovery, The Chinese University of Hong Kong, Shenzhen, and the Department of Molecular and Cellular Physiology, Stanford University School of Medicine, under the supervision of Professor Brian Kobilka, the 2012 Nobel Laureate xk星空官方网站 Chemistry. xk星空官方网站 January 2025, he joined the School of Medicine at Southern University of Science and Technology.
His research has long focused on the dynamic molecular mechanisms of G protein-coupled receptor (GPCR) signaling transduction and related drug development. To date, he has published over twenty high-quality academic papers, including research achievements as the first author or corresponding author xk星空官方网站 internationally renowned journals such as Nature, Science, Science Advances, Molecular Cell, JACS, Nature Communications, Cell Research, and PNAS. He has led multiple projects, including the National Natural Science Foundation of China and the Guangdong Provincial Excellent Youth Science Foundation.
RESEARCH: G protein-coupled receptors (GPCRs) constitute the largest family of membrane protein receptors. They perceive and respond to a diverse array of extracellular stimuli, including light, hormones, and neurotransmitters. These external signals are transduced by GPCRs into intracellular signals, which xk星空官方网站 turn regulate numerous critical physiological and pathological processes. GPCRs also represent the most successful class of drug targets.
Our research group employs a multidisciplinary research strategy, integrating chemical biology, protein engineering, molecular and cellular pharmacology, and various biophysical approaches—including nuclear magnetic resonance (NMR) spectroscopy, single-molecule fluorescence imaging, single-particle cryo-electron microscopy (cryo-EM), and hydrogen-deuterium exchange mass spectrometry (HDX-MS)—to deeply decipher the dynamic molecular basis underlying the functional diversity and complexity of GPCRs.
Furthermore, we leverage cutting-edge technologies such as DNA-encoded chemical libraries (DELs) and artificial intelligence-assisted drug design to conduct research and development on small molecule ligands targeting GPCRs—particularly biased agonists and allosteric modulators—for major health challenges like central nervous system disorders, pain, and cardiovascular diseases. Our goal is to explore novel mechanisms of drug regulation and discover new therapeutic targets, ultimately aiming to provide new strategies for the future treatment and prevention ofa broad range of diseases.
EDUCATION:
2010.09–2014.06
Huazhong University of Science and Technology
Bachelor of Science (B.S.) xk星空官方网站 Biotechnology
2014.09–2019.10
Tsinghua University
Doctor of Philosophy (Ph.D.) xk星空官方网站 Biology
WOKRING EXPERIENCE:
2020.03–2021.05
The Chinese University of Hong Kong (Shenzhen), Kobilka Institute of Innovative Drug Discovery
Visiting Scholar
2021.06–2025.01
Stanford University School of Medicine, Department of Molecular and Cellular Physiology
Postdoctoral Researcher
2025.01–2026.05
Southern University of Science and Technology (SUSTech), School of Medicine
Assistant Professor, Doctoral Supervisor
2026.06- now
Southern University of Science and Technology (SUSTech), School of Medicine
AssociateProfessor, Doctoral Supervisor
HONORS AND AWARDS:
2011, 2013
National Scholarship
2014
Outstanding Graduate, Huazhong University of Science and Technology
2017
Avanti Polar Lipids, Inc. Fellowship Award (Cold Spring Harbor Asia Conference on Membrane Protein: structure and function)
2023
Dean’s Fellowship Award, Stanford University School of Medicine
MANUSCRIPT REVIEWER AND EDITOR：
Reviewer for prestigious journals including Nature Communications, Cell Research, Cell Discovery, and Structure.
Teaching
<Physiology> (undergraduate students)
PUBLICATIONS：
(# Equal Contribution, * Corresponding)
1. Jiemin Shen#, Teja Nikhil Peddada#, Konstantin E. Komolov, Francesco De Pascali, Alexander M.Garces, Haoqing Wang, Muhammad Ehsan, Pil Seok Chae, Michael T.Lerch, Jeffrey L. Benovic, Jun Xu*, Brian K. Kobilka*. A biased allosteric modulator functions as a molecular glue to induce β2AR dimerization. Nature,2026 08.29.
2. Donghoon Ahn, Seungmi Kim, Jae Kyung Hyun, Jun Xu*, Ka Young Chung*. Ligand-specific conformational dynamics of the α2A-adrenergic xk星空官方网站 revealed by hydrogen-deuterium exchange mass spectrometry. 2026. Structure, Mar 10.
3. Jxk星空官方网站 Xu#, R. Qiu#, A. W. Garces, H. Hubner, X. Xu, D. Weikert, P. Gmeiner, M. T. Lerch, B. K. Kobilka*. The role of intrinsically disordered domains xk星空官方网站 G protein coupled receptor signaling. 2025, JACS,Oct 27.
4. G. Chen#, J. Blahova#, N. Staffen, H. Hübner, N. Nunhöfer, C. Qiu, P. Gmeiner*, D. Weikert*, Y. xk星空官方网站*, Jun Xu*. Mechanism and function of GPR3 regulated by a negative allosteric modulator. Nature Communications. 2025, August 27.
5. J. Xu#, G. Chen#, H. Wang, S. Cao, J. Heng, X. Deupi, Y. xk星空官方网站, & B. K. Kobilka. Calcineurin-fusion facilitates cryo-EM structure determination of a family A GPCR. PNAS, 2024, Nov 20.
6. G. Chen, N. Staffen, Z. Wu, X. Xu, J. Pan, A. Inoue, R. Han, P. Gmeiner*, Yang xk星空官方网站*, J. Xu*, Structural and functional characterization of the endogenous agonist for the orphan xk星空官方网站 GPR3. Cell Research. 2024, Jan 30.
7. J. Xu#, Q. Wang#, H. Hübner, Y. Hu, X. Niu, S. Maeda, A. Inoue, H. Wang, Y. Tao, P. Gmeiner, Y. xk星空官方网站, C. Jin, &B. K. Kobilka. Structural and dynamic insights into supra-physiological activation and allosteric modulation of a muscarinic receptor. Naturecommunications. 2023, Jan 23.
8. J. Xu, Y. Hu, J. Kaindl, P. Risel, H. Hübner, S. Maeda, X. Niu, H. Li, P. Gmeiner, C. Jin, B. K. Kobilka. Conformational complexity and dynamics xk星空官方网站 a muscarinic receptor revealed by NMR spectroscopy. Molecular Cell. 2019 July 11.
9. J. Xu#, S. Cao#, H. Hübner#, D. Weikert, G. Chen, Q. Lu, D. Yuan, P. Gmeiner, Z. Liu, & Y. xk星空官方网站. Structural insights into ligand recognition, activation and signaling of the α2A-adrenergic xk星空官方网站. Science Advances. 2022, March 4.
10. E. A. Fink#, J. Xu#, H. Hübner#, J. M. Braz#, P. Seemann#, C. Avet, V. Craik, M. Schmidt, C. Webb, N. A. Tolmachova, Y. S. Moroz, X. Huang, C. DeLeon, C. Kalyanaraman, S. Gahbauer, M. P. Jacobson, B. L. Roth, J. J. Irwin, Y. xk星空官方网站, B. K. Shoichet, A. I. Basbaum, & P. Gmeiner. Structure-based discovery of non-opioid analgesics acting through the α2A-adrenergic xk星空官方网站. Science, 2022, Sep 30. Highlighted by Nature Reviews Drug Discovery: “Virtual screening yields refined GPCR agonists”.
11. G. Chen#, J. Xu#, A. Inoue#, M. F. Schmidt#, C. Bai, Q. Lu, P. Gmeiner, Z. Liu, & Y. xk星空官方网站. Activation and allosteric regulation of the orphan GPR88-Gi signaling complex. Nature communications. 2022, May 2.
12. L. Wang#, J. Xu#, S. Cao, D. Sun, H. Liu, Q. Lu, Z. Liu, Y. xk星空官方网站, & C. Zhang. Cryo-EM structure of the AVP-vasopressin receptor 2-Gs signaling complex. Cell Research. 2021, Mar 4.
13. H. R. Kim#, J. Xu#, S. Maeda, N. M. Duc, D. Ahn, Y. xk星空官方网站, & K. Y. Chung. Structural mechanism of the primary and the secondary coupling between GPCRs and the Gi/o Family. Nature communications. 2020 June 22.
14. Z. Wu, G. Chen, C. Qiu, X. Yan, L. Xu, S. Jiang, J. Xu, R. Han, T. Shi, Y. Liu, W. Gao, Q. Wang, J. xk星空官方网站, F. Ye, X. Pan, Z. Zhang, P. Ning, B. Zhang, G. Chen, Y. xk星空官方网站. Structural basis for the ligand recognition and G-protein subtype selectivity of kisspeptin xk星空官方网站. Science Advances. 2024, Aug 16.
15. M. xk星空官方网站, X. Wang, J. Wang, J. Xu, W. Sun, V. A. Adediwura, Y. Miao, Y. Cheng, L. Ye. Structure and function of a ligand-free intermediate GPCR-Gabg complex. Nature communications. 2024, accepted.
16. K. K. Kumar, H. Wang, C. Habrian, N. R. Latorraca, J. Xu, E. S. O’Brien, C. Zhang, E. Montabana, A. Koehl, S. Marqusee, E. Y. Isacoff, B. K. Kobilka. Step-wise activation of a metabotropic glutamate xk星空官方网站. Nature,2024, April 17.
17. D. Ham, A. Inoue, J. Xu,Y. xk星空官方网站, K. Y. Chuang. Molecular mechanism of muscarinic acetylcholine receptor M3 interaction with Gq. Communications Biology, 2024, Mar 23.
18. D. Ahn, D. Provasi, N. M. Duc, J. Xu, L. S.-Estrada, A.Spasic, M. W.Yun, J. Kang, D. Gim, J. Lee, Y. xk星空官方网站, M. Filizola, K. Y. Chung. Gαs slow conformational transition upon GTP binding and a novel Gαs regulator. iScience. 2023 April.
19. D. Yuan, Z. Liu, J. Kaindl, S. Maeda, J. Zhao, X. Sun, J. Xu, P. Gmeiner, H. Wang, B. K. Kobilka. Activation of the α2B adrenergic xk星空官方网站 by the sedative sympatholytic dexmedetomidine. Nature Chemical Biology. 2020 March 09.
20. S. Maeda,J. Xu, F. M. N. Kadji, M. J. Clark, J. Zhao, N. Tsutsumi, R. K. Sunahara, A. Inoue, K. C. Garcia, B. K. Kobilka. Structure and selectivity engineering of the M1 muscarinic xk星空官方网站 toxin complex. Science. 2020 July 10.
21. X. Ma, Y. Hu, X. Niu, H. xk星空官方网站, J. Heng, J. Xu, X. Liu, C. Jin, B. K. Kobilka. Analysis of β2AR-Gs and β2AR-Gi complex formation by NMR spectroscopy. PNAS. 2020 Aug 31.
22. M. Korczynska, M. J. Clark, C. Valant, J. Xu, E. V. Moo, S. Albold, D. R. Weiss, H. Torosyan, W. Huang, A. C. Kruse, B. R. Lyda, L. T. May, J. Baltos, P. M. Sexton, B. K. Kobilka, A. Christopoulos, B. K. Shoichet, and R. K. Sunahara. Structure-based discovery of selective positive allosteric modulators of antagonists for the M2 muscarinic acetylcholine xk星空官方网站. PNAS. 2018 Feb 16.