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Thyroid Peroxidase as an Autoantigen in Hashimoto's Disease: Structure, Function, and Antigenicity

机译:甲状腺过氧化物酶作为哈希莫病的疾病的自身抗原:结构,功能和抗原性

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摘要

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.
机译:人甲状腺过氧化物酶(TPO),是一种重要的酶,其负责甲状腺激素的生物合成,是自身免疫性甲状腺疾病(AITDS)中的主要自身抗原,如破坏性散列瘤的甲状腺炎。虽然尚未确定TPO的结构,但其细胞外结构域由三个区域组成,这三个区域与已知的三维结构的结构域具有高度序列相似性:髓氧化酶(MPO) - 状结构域,补体对照蛋白(CCP) - 状结构域,表皮生长因子(EGF) - 状结构域。因此,可以构建TPO的同源模型,为其已知功能提供一些结构上下文,以及促进对其自身抗炎性负责的区域的映射。在本综述中,我们突出了该领域的最近进展,特别是分子建模方法如何先进的TPO对表位映射研究的可视化和解释,促进了TPO蛋白质结构,功能和自身征密性之间的相互作用的解剖。

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