G Protein-Coupled Receptors: What a Difference a 'Partner' Makes

被引:27
作者
Roux, Benoit T. [1 ]
Cottrell, Graeme S. [2 ]
机构
[1] Univ Bath, Dept Pharm & Pharmacol, Bath BA2 7AY, Avon, England
[2] Univ Reading, Reading Sch Pharm, Reading RG6 6UB, Berks, England
基金
英国生物技术与生命科学研究理事会;
关键词
interacting protein; escort protein; GPCR; signaling modulation; chaperone; trafficking; accessory protein; GENE-RELATED PEPTIDE; ACTIVITY-MODIFYING PROTEINS; CYCLOPHILIN HOMOLOG NINAA; BINDING PHOSPHOPROTEIN-50 EBP50; V2 VASOPRESSIN RECEPTOR; PDZ SCAFFOLD NHERF-2; CALCITONIN-RECEPTOR; ENDOPLASMIC-RETICULUM; BETA-ARRESTIN; SIGNAL-TRANSDUCTION;
D O I
10.3390/ijms15011112
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
G protein-coupled receptors (GPCRs) are important cell signaling mediators, involved in essential physiological processes. GPCRs respond to a wide variety of ligands from light to large macromolecules, including hormones and small peptides. Unfortunately, mutations and dysregulation of GPCRs that induce a loss of function or alter expression can lead to disorders that are sometimes lethal. Therefore, the expression, trafficking, signaling and desensitization of GPCRs must be tightly regulated by different cellular systems to prevent disease. Although there is substantial knowledge regarding the mechanisms that regulate the desensitization and down-regulation of GPCRs, less is known about the mechanisms that regulate the trafficking and cell-surface expression of newly synthesized GPCRs. More recently, there is accumulating evidence that suggests certain GPCRs are able to interact with specific proteins that can completely change their fate and function. These interactions add on another level of regulation and flexibility between different tissue/cell-types. Here, we review some of the main interacting proteins of GPCRs. A greater understanding of the mechanisms regulating their interactions may lead to the discovery of new drug targets for therapy.
引用
收藏
页码:1112 / 1142
页数:31
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