Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts.
Endocrinology. 2020 Feb 1;161(2). doi: 10.1210/endocr/bqaa016.
Thyroid peroxidase (TPO) is a critical membrane-bound enzyme involved in the biosynthesis of multiple thyroid hormones, and is a major autoantigen in autoimmune thyroid diseases such as destructive (Hashimoto) thyroiditis. Here we report the biophysical and structural characterization of a novel TPO construct containing only the ectodomain of TPO and lacking the propeptide. The construct was enzymatically active and able to bind the patient-derived TR1.9 autoantibody. Analytical ultracentrifugation data suggest that TPO can exist as both a monomer and a dimer. Combined with negative stain electron microscopy and molecular dynamics simulations, these data show that the TR1.9 autoantibody preferentially binds the TPO monomer, revealing conformational changes that bring together previously disparate residues into a continuous epitope. In addition to providing plausible structural models of a TPO-autoantibody complex, this study provides validated TPO constructs that will facilitate further characterization, and advances our understanding of the structural, functional, and antigenic characteristics of TPO, an autoantigen implicated in some of the most common autoimmune diseases.
甲状腺过氧化物酶(TPO)是一种重要的膜结合酶,参与多种甲状腺激素的生物合成,是破坏性(桥本)甲状腺炎等自身免疫性甲状腺疾病的主要自身抗原。在这里,我们报告了一种新型 TPO 结构的生物物理和结构特征,该结构仅包含 TPO 的胞外结构域,缺乏前肽。该构建体具有酶活性,能够结合患者来源的 TR1.9 自身抗体。分析超速离心数据表明,TPO 可以以单体和二聚体的形式存在。结合负染电子显微镜和分子动力学模拟,这些数据表明 TR1.9 自身抗体优先结合 TPO 单体,揭示了使先前不同的残基聚集在一起形成连续表位的构象变化。除了提供 TPO-自身抗体复合物的合理结构模型外,这项研究还提供了经过验证的 TPO 构建体,这将有助于进一步的表征,并推进我们对 TPO 的结构、功能和抗原特性的理解,TPO 是一些最常见的自身免疫性疾病中涉及的自身抗原。