6X59
The mouse cGAS catalytic domain binding to human assembled nucleosome
Summary for 6X59
| Entry DOI | 10.2210/pdb6x59/pdb |
| EMDB information | 22046 |
| Descriptor | Histone H3.2, Histone H4, Histone H2A type 1, ... (8 entities in total) |
| Functional Keywords | immunity, dna binding protein-dna-transferase complex, dna binding protein/dna/transferase |
| Biological source | Homo sapiens (Human) More |
| Total number of polymer chains | 11 |
| Total formula weight | 243077.34 |
| Authors | Pengbiao, X.,Pingwei, L.,Baoyu, Z. (deposition date: 2020-05-25, release date: 2020-09-16, Last modification date: 2024-05-15) |
| Primary citation | Zhao, B.,Xu, P.,Rowlett, C.M.,Jing, T.,Shinde, O.,Lei, Y.,West, A.P.,Liu, W.R.,Li, P. The molecular basis of tight nuclear tethering and inactivation of cGAS. Nature, 587:673-677, 2020 Cited by PubMed Abstract: Nucleic acids derived from pathogens induce potent innate immune responses. Cyclic GMP-AMP synthase (cGAS) is a double-stranded DNA sensor that catalyses the synthesis of the cyclic dinucleotide cyclic GMP-AMP, which mediates the induction of type I interferons through the STING-TBK1-IRF3 signalling axis. cGAS was previously thought to not react with self DNA owing to its cytosolic localization; however, recent studies have shown that cGAS is localized mostly in the nucleus and has low activity as a result of tight nuclear tethering. Here we show that cGAS binds to nucleosomes with nanomolar affinity and that nucleosome binding potently inhibits its catalytic activity. To elucidate the molecular basis of cGAS inactivation by nuclear tethering, we determined the structure of mouse cGAS bound to human nucleosome by cryo-electron microscopy. The structure shows that cGAS binds to a negatively charged acidic patch formed by histones H2A and H2B via its second DNA-binding site. High-affinity nucleosome binding blocks double-stranded DNA binding and maintains cGAS in an inactive conformation. Mutations of cGAS that disrupt nucleosome binding alter cGAS-mediated signalling in cells. PubMed: 32911481DOI: 10.1038/s41586-020-2749-z PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (2.98 Å) |
Structure validation
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