Molecular mechanisms linking geranylgeranyl diphosphate synthase to cell survival and proliferation.

Q3 Biochemistry, Genetics and Molecular Biology Molecular Membrane Biology Pub Date : 2016-03-01 Epub Date: 2016-08-18 DOI:10.1080/09687688.2016.1213432
Sherry S Agabiti, Yilan Liang, Andrew J Wiemer
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引用次数: 17

Abstract

Geranylgeranyl diphosphate is a 20-carbon isoprenoid phospholipid whose lipid moiety can be post-translationally incorporated into proteins to promote membrane association. The process of geranylgeranylation has been implicated in anti-proliferative effects of clinical agents that inhibit enzymes of the mevalonate pathway (i.e. statins and nitrogenous bisphosphonates) as well as experimental agents that deplete geranylgeranyl diphosphate. Inhibitors of geranylgeranyl diphosphate synthase are an attractive way to block geranylgeranylation because they possess a calcium-chelating substructure to allow localization to bone and take advantage of a unique position of the enzyme within the biosynthetic pathway. Here, we describe recent advances in geranylgeranyl diphosphate synthase expression and inhibitor development with a particular focus on the molecular mechanisms that link geranylgeranyl diphosphate to cell proliferation via geranylgeranylated small GTPases.

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香叶二磷酸合酶与细胞存活和增殖的分子机制。
香叶二磷酸是一种20碳类异戊二烯磷脂,其脂质部分可翻译后并入蛋白质中以促进膜结合。geranylgeranyation的过程与抑制甲羟戊酸途径酶的临床药物(即他汀类药物和含氮双膦酸盐)以及消耗geranylgeranyl二磷酸的实验药物的抗增殖作用有关。香叶香叶二磷酸合成酶抑制剂是阻断香叶香叶酰化的一种有吸引力的方法,因为它们具有钙螯合亚结构,允许定位到骨骼,并利用酶在生物合成途径中的独特位置。在这里,我们描述了香叶二磷酸合酶表达和抑制剂开发的最新进展,特别关注通过香叶二磷酸化小gtp酶将香叶二磷酸与细胞增殖联系起来的分子机制。
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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来源期刊
Molecular Membrane Biology
Molecular Membrane Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation. Molecular Membrane Biology provides a forum for high quality research that serves to advance knowledge in molecular aspects of biological membrane structure and function. The journal welcomes submissions of original research papers and reviews in the following areas: • Membrane receptors and signalling • Membrane transporters, pores and channels • Synthesis and structure of membrane proteins • Membrane translocation and targeting • Lipid organisation and asymmetry • Model membranes • Membrane trafficking • Cytoskeletal and extracellular membrane interactions • Cell adhesion and intercellular interactions • Molecular dynamics and molecular modelling of membranes. • Antimicrobial peptides.
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