Williams Daniel E, Le Sarah N, Godlewska Marlena, Hoke David E, Buckle Ashley M
Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria, Australia.
Department of Biochemistry and Molecular Biology, Center of Postgraduate Medical Education, Warsaw, Poland.
Horm Metab Res. 2018 Dec;50(12):908-921. doi: 10.1055/a-0717-5514. Epub 2018 Oct 25.
Human thyroid peroxidase (TPO), is an important enzyme responsible for the biosynthesis of thyroid hormones and is a major autoantigen in autoimmune thyroid diseases (AITDs) such as the destructive Hashimoto's thyroiditis. Although the structure of TPO has yet to be determined, its extracellular domain consists of three regions that exhibit a high degree of sequence similarity to domains of known three-dimensional structure: the myeloperoxidase (MPO)-like domain, complement control protein (CCP)-like domain, and epidermal growth factor (EGF)-like domain. Homology models of TPO can therefore be constructed, providing some structural context to its known function, as well as facilitating the mapping of regions that are responsible for its autoantigenicity. In this review, we highlight recent progress in this area, in particular how a molecular modelling approach has advanced the visualisation and interpretation of epitope mapping studies for TPO, facilitating the dissection of the interplay between TPO protein structure, function, and autoantigenticity.
人甲状腺过氧化物酶(TPO)是一种负责甲状腺激素生物合成的重要酶,并且是自身免疫性甲状腺疾病(AITD)(如破坏性桥本甲状腺炎)中的主要自身抗原。尽管TPO的结构尚未确定,但其细胞外结构域由三个区域组成,这些区域与已知三维结构的结构域具有高度的序列相似性:髓过氧化物酶(MPO)样结构域、补体控制蛋白(CCP)样结构域和表皮生长因子(EGF)样结构域。因此,可以构建TPO的同源模型,为其已知功能提供一些结构背景,同时有助于确定负责其自身抗原性的区域。在这篇综述中,我们重点介绍了该领域的最新进展,特别是分子建模方法如何推进了TPO表位作图研究的可视化和解释,促进了对TPO蛋白结构、功能和自身抗原性之间相互作用的剖析。