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G蛋白偶联受体的转运:理解健康与疾病的化学基础。

G-protein-coupled receptor trafficking: understanding the chemical basis of health and disease.

作者信息

Ulloa-Aguirre Alfredo, Janovick Jo Ann, Miranda Alfredo Leaños, Conn P Michael

机构信息

Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, Oregon 97006, USA.

出版信息

ACS Chem Biol. 2006 Nov 21;1(10):631-8. doi: 10.1021/cb600360h.

Abstract

The primary function of cell surface receptors is to recognize specific chemical signals from other substances and produce a biological response. Point mutations in cell surface receptors may result in production of misfolded proteins that are translated but do not reach their proper functional destination in the cell. Also, for some G-protein-coupled receptors, large amounts of wild-type receptor may be destroyed without arriving at the plasma membrane (PM). For the human gonadotropin-releasing hormone receptor, this "inefficiency" has resulted from strong and convergent evolutionary pressure, producing receptor molecules that are sensitive to single changes in chemical charge and are delicately balanced between expression at the PM or retention/degradation in the endoplasmic reticulum. This Perspective focuses on the evolved mechanisms that control PM expression of this receptor at this post-translational level.

摘要

细胞表面受体的主要功能是识别来自其他物质的特定化学信号并产生生物学反应。细胞表面受体中的点突变可能导致错误折叠蛋白的产生,这些蛋白虽已翻译但无法在细胞中到达其正常的功能目的地。此外,对于一些G蛋白偶联受体,大量野生型受体可能在未到达质膜(PM)之前就被破坏。对于人类促性腺激素释放激素受体而言,这种“低效性”是由强大且趋同的进化压力导致的,产生的受体分子对化学电荷的单一变化敏感,并且在质膜表达或在内质网中滞留/降解之间微妙地平衡。本观点聚焦于在翻译后水平控制该受体质膜表达的进化机制。

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