Virus-encoded G-protein-coupled receptors: constitutively active (dys)regulators of cell function and their potential as drug target.

H F Vischer, J W Hulshof, I J P de Esch, M J Smit, R Leurs
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引用次数: 13

Abstract

G-protein-coupled receptors encoded by herpesviruses such as EBV, HCMV and KSHV are very interesting illustrations of the (patho)physiological importance of constitutive GPCR activity. These viral proteins are expressed on the cell surface of infected cells and often constitutively activate a variety of G-proteins. For some virus-encoded GPCRs, the constitutive activity has been shown to occur in vivo, i.e., in infected cells. In this paper, we will review the occurrence of virus-encoded GPCRs and describe their known signaling properties. Moreover, we will also review the efforts, directed towards the discovery of small molecule antagonist, that so far have been mainly focused on the HCMV-encoded GPCR US28. This virus-encoded receptor might be involved in cardiovascular diseases and cancer and seems an interesting target for drug intervention.

病毒编码的g蛋白偶联受体:细胞功能的组成活性(日)调节剂及其作为药物靶点的潜力。
由eb病毒、HCMV和KSHV等疱疹病毒编码的g蛋白偶联受体是组成型GPCR活性(病理)生理重要性的非常有趣的例证。这些病毒蛋白在感染细胞的细胞表面表达,通常组成性地激活多种g蛋白。对于一些病毒编码的gpcr,其组成活性已被证明发生在体内,即在感染细胞中。在本文中,我们将回顾病毒编码gpcr的发生,并描述其已知的信号特性。此外,我们还将回顾迄今为止主要集中在hcmv编码GPCR US28上的小分子拮抗剂的发现。这种病毒编码受体可能与心血管疾病和癌症有关,似乎是药物干预的有趣靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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