KG Jebsen Coeliac Disease Research Centre, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Department of Immunology, Oslo University Hospital-Rikshospitalet, Oslo, Norway.
Nat Commun. 2023 Oct 5;14(1):6216. doi: 10.1038/s41467-023-42004-z.
Transglutaminase 3 (TG3), the autoantigen of dermatitis herpetiformis (DH), is a calcium dependent enzyme that targets glutamine residues in polypeptides for either transamidation or deamidation modifications. To become catalytically active TG3 requires proteolytic cleavage between the core domain and two C-terminal β-barrels (C1C2). Here, we report four X-ray crystal structures representing inactive and active conformations of human TG3 in complex with a TG3-specific Fab fragment of a DH patient derived antibody. We demonstrate that cleaved TG3, upon binding of a substrate-mimicking inhibitor, undergoes a large conformational change as a β-sheet in the catalytic core domain moves and C1C2 detaches. The unique enzyme-substrate conformation of TG3 without C1C2 is recognized by DH autoantibodies. The findings support a model where B-cell receptors of TG3-specific B cells bind and internalize TG3-gluten enzyme-substrate complexes thereby facilitating gluten-antigen presentation, T-cell help and autoantibody production.
转谷氨酰胺酶 3(TG3)是疱疹样皮炎(DH)的自身抗原,是一种依赖钙的酶,可针对多肽中的谷氨酰胺残基进行转酰胺或脱酰胺修饰。为了具有催化活性,TG3 需要在核心结构域和两个 C 端β桶(C1C2)之间进行蛋白水解切割。在这里,我们报告了四个 X 射线晶体结构,代表了与来自 DH 患者来源抗体的 TG3 特异性 Fab 片段形成复合物的人 TG3 的非活性和活性构象。我们证明,在结合底物模拟抑制剂后,经切割的 TG3 会发生较大的构象变化,催化核心结构域中的β-片层移动,C1C2 分离。DH 自身抗体识别无 C1C2 的 TG3 独特的酶-底物构象。这些发现支持了这样一种模型,即 TG3 特异性 B 细胞的 B 细胞受体结合并内化 TG3-谷氨酰胺酶-底物复合物,从而促进谷氨酰胺抗原呈递、T 细胞辅助和自身抗体产生。