化EM揭示了人类AIM/CD5L识别聚合物免疫球蛋白M的结构基础
Qu Chen1, Kazuhiro Ishii2,3, Haruka Mori2
1Structural Biology Science Technology Platform, The Francis Crick Institute, London, UK.
Nature communications
|October 31, 2024
概括
巨细胞的亡抑制剂 (AIM) 与IgM和损伤相关分子模式 (DAMPs) 结合. 冷电子显微镜揭示了AIM如何使用AIM.
科学领域:
- 免疫学 免疫学 免疫学
- 结构生物学 结构生物学
- 生物化学 生化学
背景情况:
- 细胞表面清洁者受体维持稳态,并对病原体和损伤做出反应.
- 巨细胞的亡抑制剂 (AIM/CD5L),一种食受体氨酸丰富 (SRCR) 超级蛋白质,可以预防与感染,炎症和癌症相关的疾病.
- 艾姆与IgM五聚体形成复合体,维持激活的血清水平.
研究的目的:
- 阐明对IgM和其他有约束力的目标的AIM认可的结构性基础.
- 了解AIM如何与IgM和损伤相关分子模式 (DAMPs) 相互作用.
主要方法:
- 使用冷电子显微镜 (cryo-EM) 进行成像.
- 对AIM-IgM相互作用的结构分析.
主要成果:
- 冷EM揭示了AIM的C端SRCR域与IgM核心的Fcμ常数区域和J链之间的相互作用.
- AIM的两个SRCR接口对于与损伤相关的分子模式 (DAMPs) 结合至关重要.
结论:
- 这项研究为IgM的AIM认可提供了第一个结构性见解.
- AIM利用其SRCR域与IgM和DAMP相互作用,突出其在免疫反应中的多功能作用.
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