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乳糜泻中转谷氨酰胺酶2特异性自身抗体识别抗原的结构基础

Structural Basis for Antigen Recognition by Transglutaminase 2-specific Autoantibodies in Celiac Disease.

作者信息

Chen Xi, Hnida Kathrin, Graewert Melissa Ann, Andersen Jan Terje, Iversen Rasmus, Tuukkanen Anne, Svergun Dmitri, Sollid Ludvig M

机构信息

From the Centre for Immune Regulation and Department of Immunology, University of Oslo and Oslo University Hospital, N-0372 Oslo, Norway and.

European Molecular Biology Laboratory, Hamburg Outstation, D-22607 Hamburg, Germany.

出版信息

J Biol Chem. 2015 Aug 28;290(35):21365-75. doi: 10.1074/jbc.M115.669895. Epub 2015 Jul 9.

Abstract

Antibodies to the autoantigen transglutaminase 2 (TG2) are a hallmark of celiac disease. We have studied the interaction between TG2 and an anti-TG2 antibody (679-14-E06) derived from a single gut IgA plasma cell of a celiac disease patient. The antibody recognizes one of four identified epitopes targeted by antibodies of plasma cells of the disease lesion. The binding interface was identified by small angle x-ray scattering, ab initio and rigid body modeling using the known crystal structure of TG2 and the crystal structure of the antibody Fab fragment, which was solved at 2.4 Å resolution. The result was confirmed by testing binding of the antibody to TG2 mutants by ELISA and surface plasmon resonance. TG2 residues Arg-116 and His-134 were identified to be critical for binding of 679-14-E06 as well as other epitope 1 antibodies. In contrast, antibodies directed toward the two other main epitopes (epitopes 2 and 3) were not affected by these mutations. Molecular dynamics simulations suggest interactions of 679-14-E06 with the N-terminal domain of TG2 via the CDR2 and CDR3 loops of the heavy chain and the CDR2 loop of the light chain. In addition there were contacts of the framework 3 region of the heavy chain with the catalytic domain of TG2. The results provide an explanation for the biased usage of certain heavy and light chain gene segments by epitope 1-specific antibodies in celiac disease.

摘要

针对自身抗原转谷氨酰胺酶2(TG2)的抗体是乳糜泻的一个标志。我们研究了TG2与一种源自乳糜泻患者单个肠道IgA浆细胞的抗TG2抗体(679 - 14 - E06)之间的相互作用。该抗体识别疾病病变部位浆细胞抗体所靶向的四个已确定表位中的一个。通过小角X射线散射、利用TG2的已知晶体结构和抗体Fab片段的晶体结构(分辨率为2.4 Å)进行从头算和刚体建模确定了结合界面。通过ELISA和表面等离子体共振测试该抗体与TG2突变体的结合来证实结果。已确定TG2残基Arg - 116和His - 134对于679 - 14 - E06以及其他表位1抗体的结合至关重要。相比之下,针对另外两个主要表位(表位2和表位3)的抗体不受这些突变的影响。分子动力学模拟表明679 - 14 - E06通过重链的CDR2和CDR3环以及轻链的CDR2环与TG2的N端结构域相互作用。此外,重链的框架3区域与TG2的催化结构域存在接触。这些结果为乳糜泻中表位1特异性抗体对某些重链和轻链基因片段的偏向性使用提供了解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f041/4571865/5e5219bcdb0a/zbc0391524560001.jpg

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