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Structure and Function of Thyroid Hormone Plasma Membrane Transporters

机译:甲状腺激素血浆膜转运蛋白的结构和功能

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摘要

Thyroid hormones (TH) cross the plasma membrane with the help of transporter proteins. As charged amino acid derivatives, TH cannot simply diffuse across a lipid bilayer membrane, despite their notorious hydrophobicity. The identification of monocarboxylate transporter 8 (MCT8, SLC16A2) as a specific and very active TH transporter paved the way to the finding that mutations in the MCT8 gene cause a syndrome of psychomotor retardation in humans. The purpose of this review is to introduce the current model of transmembrane transport and highlight the diversity of TH transmembrane transporters. The interactions of TH with plasma transfer proteins, T3 receptors, and deiodinase are summarized. It is shown that proteins may bind TH owing to their hydrophobic character in hydrophobic cavities and/or by specific polar interaction with the phenolic hydroxyl, the aminopropionic acid moiety, and by weak polar interactions with the iodine atoms. These findings are compared with our understanding of how TH transporters interact with substrate. The presumed effects of mutations in MCT8 on protein folding and transport function are explained in light of the available homology model.
机译:甲状腺激素(TH)在转运蛋白的帮助下穿过质膜。作为带电荷的氨基酸衍生物,尽管臭名昭著的疏水性,TH不能简单地在脂质双层膜上扩散。单羧酸盐转运蛋白8(MCT8,SLC16A2)的鉴定为特异性和非常活跃的TH转运蛋白,为发现MCT8基因突变引起人类精神运动迟钝综合征的发现铺平了道路。这篇综述的目的是介绍当前的跨膜转运模型,并强调TH跨膜转运蛋白的多样性。总结了TH与血浆转移蛋白,T3受体和脱碘酶的相互作用。已经表明,由于它们在疏水腔中的疏水特性和/或通过与酚羟基,氨基丙酸部分的特定极性相互作用以及通过与碘原子的弱极性相互作用,蛋白质可以结合TH。将这些发现与我们对TH转运蛋白如何与底物相互作用的理解进行了比较。根据可用的同源性模型解释了MCT8突变对蛋白质折叠和转运功能的推测影响。

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