Agabiti Sherry S, Liang Yilan, Wiemer Andrew J
a Department of Pharmaceutical Sciences , University of Connecticut , Storrs , CT , USA.
b Institute for Systems Genomics, University of Connecticut , Storrs , CT , USA.
Mol Membr Biol. 2016 Mar;33(1-2):1-11. doi: 10.1080/09687688.2016.1213432. Epub 2016 Aug 18.
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.
香叶基香叶基二磷酸是一种含有20个碳原子的类异戊二烯磷脂,其脂质部分可在翻译后掺入蛋白质中以促进膜结合。香叶基香叶基化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)以及消耗香叶基香叶基二磷酸的实验药物的抗增殖作用有关。香叶基香叶基二磷酸合酶抑制剂是阻断香叶基香叶基化的一种有吸引力的方法,因为它们具有钙螯合亚结构,可使其定位于骨骼,并利用该酶在生物合成途径中的独特位置。在此,我们描述了香叶基香叶基二磷酸合酶表达和抑制剂开发的最新进展,特别关注通过香叶基香叶基化的小GTP酶将香叶基香叶基二磷酸与细胞增殖联系起来的分子机制。