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8Z37

Crystal structure of human STING ligand binding domain.

Summary for 8Z37
Entry DOI10.2210/pdb8z37/pdb
DescriptorStimulator of interferon genes protein, CHLORIDE ION, CALCIUM ION, ... (5 entities in total)
Functional Keywordscgamp binding protein, immune system
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight22354.56
Authors
Sun, P.K.,Li, X.J. (deposition date: 2024-04-14, release date: 2025-04-16, Last modification date: 2025-10-22)
Primary citationSun, P.,Wang, B.,Liu, C.,Wang, Z.,Liu, Y.,Qiao, Y.B.,Li, X.
A fluorescent STING ligand sensor for high-throughput screening of compounds that can enhance tumor immunotherapy.
Cell Rep Methods, 5:101106-101106, 2025
Cited by
PubMed Abstract: The activation of the stimulator of interferon genes (STING) pathway triggers the release of type I interferons that can potentiate the host immune response against tumors. STING agonism is therefore a promising strategy for the development of cancer immunotherapy; however, sensitive tools and assays for the discovery of STING modulators are currently limited. Here, we develop and characterize a STING ligand sensor, FiSL, to detect STING ligands in vitro. Utilizing FiSL, we identify honokiol, a natural compound derived from Magnolia species, as an orally available STING agonist from a bioactive compound library. Functional studies reveal that honokiol exerts antitumor activity in a STING-dependent manner. Moreover, in STING-humanized mouse tumor models, honokiol enhances the efficacy of anti-PD-(L)1 immunotherapy. Collectively, we have developed FiSL as a tool for high-throughput screening of STING ligands and revealed honokiol as a STING agonist that can be harnessed to treat human cancer.
PubMed: 40669456
DOI: 10.1016/j.crmeth.2025.101106
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.4 Å)
Structure validation

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