8W6P

Crystal structure of dimeric murine SMPDL3A

8W6P の概要

• エントリーDOI: 10.2210/pdb8w6p/pdb
• 分子名称: Acid sphingomyelinase-like phosphodiesterase 3a, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, alpha-L-fucopyranose-(1-6)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (10 entities in total)
• 機能のキーワード: innate immunity, lipid metabolism, hydrolase
• 由来する生物種: Mus musculus (house mouse)
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 97210.11

構造登録者

Zhang, C.,Liu, P.,Fan, S.,Hou, Y. (登録日: 2023-08-29, 公開日: 2023-12-20, 最終更新日: 2024-10-16)

主引用文献

Hou, Y.,Wang, Z.,Liu, P.,Wei, X.,Zhang, Z.,Fan, S.,Zhang, L.,Han, F.,Song, Y.,Chu, L.,Zhang, C.
SMPDL3A is a cGAMP-degrading enzyme induced by LXR-mediated lipid metabolism to restrict cGAS-STING DNA sensing.
Immunity, 56:2492-2507.e10, 2023

PubMed Abstract: Lipid metabolism has been associated with the cyclic guanosine monophosphate (GMP)-AMP synthase (cGAS) stimulator of interferon genes (STING) DNA-sensing pathway, but our understanding of how these signals are integrated into a cohesive immunometabolic program is lacking. Here, we have identified liver X receptor (LXR) agonists as potent inhibitors of STING signaling. We show that stimulation of lipid metabolism by LXR agonists specifically suppressed cyclic GMP-AMP (cGAMP)-STING signaling. Moreover, we developed cyclic dinucleotide-conjugated beads to biochemically isolate host effectors for cGAMP inhibition, and we found that LXR ligands stimulated the expression of sphingomyelin phosphodiesterase acid-like 3A (SMPDL3A), which is a 2'3'-cGAMP-degrading enzyme. Results of crystal structures suggest that cGAMP analog induces dimerization of SMPDL3A, and the dimerization is critical for cGAMP degradation. Additionally, we have provided evidence that SMPDL3A cleaves cGAMP to restrict STING signaling in cell culture and mouse models. Our results reveal SMPDL3A as a cGAMP-specific nuclease and demonstrate a mechanism for how LXR-associated lipid metabolism modulates STING-mediated innate immunity.

PubMed: 37890481
DOI: 10.1016/j.immuni.2023.10.001

実験手法

X-RAY DIFFRACTION (1.91 Å)