Role of GPCRs towards Cell: An explanation of G-Protein Coupled Receptor Structure

A. Sahdev, Nidhi Sharma, V. Raj
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Abstract

The molecular framework means the plasma membrane which is made up of phospholipid bilayer consist of Gprotein coupled receptor. The name GPCR refers to a common mode of receptor signalling via GTPbinding protein on the inside of the cells. Because their polypeptide chain passes seven times through the plasma membrane, GPCRs are also called as SEVENTRANSMEMBRANE (7TM) receptor. 7TM receptors mediate the physiological signals from the outside of the cells. Then these signal can be a change in the concentration of protein, lipid, neurotransmitters, ions, hormones, odourants, tastants, etc., or an influx to the eye. GPCRs transform these signals to the inside of the cells and elicit a series of reactions involving other nucleotide, protein and metal ions, which eventually deliver a message and appropriate cellular and physiological response1,2 (Figure 1). Receptor is a molecule on or in a cell with which a drug, hormones, neurotransmitters etc. can initially interacts. GProtein coupled receptors are heptahelical, serpentine receptor and are multifunctional receptor having a lots of clinical implications.3
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gpcr在细胞中的作用:对g蛋白偶联受体结构的解释
分子框架是指由磷脂双分子层组成的质膜,由g蛋白偶联受体组成。GPCR的名称是指通过细胞内部的GTPbinding蛋白传递受体信号的一种常见模式。由于其多肽链穿过质膜7次,因此也被称为7 -跨膜受体(7TM)。7TM受体介导来自细胞外部的生理信号。然后,这些信号可能是蛋白质、脂质、神经递质、离子、激素、气味剂、味觉剂等浓度的变化,或者流入眼睛。GPCRs将这些信号转化到细胞内部,引发一系列涉及其他核苷酸、蛋白质和金属离子的反应,最终传递信息和适当的细胞和生理反应1,2(图1)。受体是细胞上或细胞内的一种分子,药物、激素、神经递质等最初可以与之相互作用。g蛋白偶联受体是七螺旋、蛇形受体,是一种多功能受体,具有广泛的临床应用价值
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