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Jinpeng Sun
sunjinpeng@bjmu.edu.cn
Chinese, English
Beijing
Peking University
Basic Medical Sciences
  • 1993-1998: Bachelor in Biology and Computer Science, University of Science and Technology of China
  • 1998-2001: Master's Degree, University of Science and Technology of China
  • 2001-2007: PhD, Albert Einstein College of Medicine, Supervisor: Zhong-yin Zhang
  • Postdoctoral Researcher at Duke University, Supervisors: Robert J. Lefkowitz, James B.
  • 2007-2011: Postdoctoral Researcher, Duke University
  • Current: Professor at Peking University, Director of the Department of Biophysics
  • 2018: National Outstanding Youth Fund (Pharmacology)
  • 2023: New Keystone Project Researcher
  • 2022: Tan Jiazhen Life Science Innovation Award
  • 2022: Second Prize of Chinese Medical Science and Technology Award (Medical Science and Technology)
  • 2023: Third National Innovation Competition Award
GPCR ligand discovery and interaction mechanisms
GPCR roles in metabolic diseases like diabetes, reproduction, hearing, kidney diseases, and bone development
Pharmacological theories of GPCR preferential signaling
Transmembrane signaling in tissue reconstitution
  • Structural and signaling mechanism of TAAR1 enabled preferential agonist design, Sun JP et al., 2023
  • Ligand recognition and G-protein coupling of trace amine receptor TAAR1, Sun JP et al., 2023
  • Structural basis of amine odorant perception by a mammal olfactory receptor, Sun JP et al., 2023
  • Unsaturated bond recognition leads to biased signal in a fatty acid receptor, Sun JP et al., 2023
  • Structural basis for the tethered peptide activation of adhesion GPCRs, Sun JP et al., 2022
  • Structure, function and pharmacology of human itch receptor complexes, Sun JP et al., 2021
  • Structures of the glucocorticoid-bound adhesion receptor GPR97-Go complex, Sun JP et al., 2021
  • Tethered peptide activation mechanism of the adhesion GPCRs ADGRG2 and ADGRG4, Sun JP et al., 2022
  • Structural basis of GPBAR activation and bile acid recognition, Sun JP et al., 2020
  • Ligand recognition and allosteric regulation of DRD1-Gs signaling complexes, Sun JP et al., 2021
  • Cryo-EM structure of the X-linked acrogigantism-related orphan GPR101-Gs complex enabled identification of ligands with rejuvenating potential, Sun JP et al., 2023
  • Structures of the ADGRG2-Gs complex in apo and ligand-bound forms, Sun JP et al., 2022
  • Allosteric mechanisms underlie GPCR signaling to SH3-domain proteins through arrestin, Sun JP et al., 2018
  • Autonomous sensing of the insulin peptide by an olfactory G protein-coupled receptor modulates glucose metabolism, Sun JP et al., 2022
  • Functional screening and rational design of compounds targeting GPR132 to treat diabetes, Sun JP et al., 2023
  • Nidogen-2 is a Novel Endogenous Ligand of LGR4 to Inhibit Vascular Calcification, Sun JP et al., 2022
  • Progesterone activates GPR126 to promote breast cancer development via the Gi pathway, Sun JP et al., 2022
  • Single hormone or synthetic agonist induces Gs/Gi coupling selectivity of EP receptors via distinct binding modes and propagating paths, Sun JP et al., 2023
  • Activation of PTH1R alleviates epididymitis and orchitis through Gq and β-arrestin-1 pathways, Sun JP et al., 2021
  • Scaffolding mechanism of arrestin-2 in the cRaf/MEK1/ERK signaling cascade, Sun JP et al., 2021
  • Structural basis and molecular mechanism of biased GPBAR signaling in regulating NSCLC cell growth via YAP activity, Sun JP et al., 2022
  • Cartilage oligomeric matrix protein is an endogenous β-arrestin-2-selective allosteric modulator of AT1 receptor counteracting vascular injury, Sun JP et al., 2021
  • The catalytic region and PEST domain of PTPN18 distinctly regulate the HER2 phosphorylation and ubiquitination barcodes, Sun JP et al., 2014
  • Ligand recognition and G protein coupling of the human itch receptor MRGPRX1, Sun JP et al., 2023
  • Structural studies of phosphorylation-dependent interactions between the V2R receptor and arrestin-2, Sun JP et al., 2021
  • DeSiphering receptor core-induced and ligand-dependent conformational changes in arrestin via genetic encoded trimethylsilyl 1H-NMR probe, Sun JP et al., 2020
  • Homocysteine directly interacts and activates the angiotensin II type I receptor to aggravate vascular injury, Sun JP et al., 2018
  • Arrestin biased GPCR agonism induces acute catecholamine secretion through TRPC3 coupling, Sun JP et al., 2017
  • Phospho-selective mechanisms of arrestin conformations and functions revealed by unnatural amino acid incorporation and 19F-NMR, Sun JP et al., 2015
  • Activation pathway of a G protein-coupled receptor uncovers conformational intermediates as targets for allosteric drug design, Sun JP et al., 2021
  • Ligand recognition, unconventional activation and G protein coupling of the prostaglandin E2 receptor 2 (EP2), Sun JP et al., 2021
  • Deafness-Associated ADGRV1 Mutation Impairs USH2A Stability through Improper Phosphorylation of WHRN and WDSUB1 Recruitment, Sun JP et al., 2023
  • In vitro expansion of pancreatic islet clusters facilitated by hormones and chemicals, Sun JP et al., 2020
  • Construction of an alkaline phosphatase-specific two-photon probe and its imaging application in living cells and tissues, Sun JP et al., 2017
Gpcr Ligand Discovery Interaction Metabolic Diseases Diabetes Pharmacology Signaling Transmembrane Tissue Reconstitution

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