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培养的人细胞中香叶基二磷酸水平的定量测定。

Quantitative determination of geranyl diphosphate levels in cultured human cells.

作者信息

Holstein Sarah A, Tong Huaxiang, Kuder Craig H, Hohl Raymond J

机构信息

Department of Internal Medicine, SE 313 GH, University of Iowa, Iowa City, IA, 52242, USA.

出版信息

Lipids. 2009 Nov;44(11):1055-62. doi: 10.1007/s11745-009-3355-x. Epub 2009 Oct 24.

DOI:10.1007/s11745-009-3355-x
PMID:19856009
Abstract

Geranyl diphosphate (GPP), a 10-carbon isoprenoid, is a key intermediate in the isoprenoid biosynthetic pathway. This pathway, in addition to leading to sterol synthesis, results in the synthesis of farnesyl diphosphate (FPP) and geranylgeranyl diphosphate (GGPP), which serve as substrates for protein isoprenylation reactions. Basal levels of GPP in mammalian cells previously have been undetectable. Here we present a novel, sensitive, nonradioactive method which allows for measurement of GPP in mammalian cells. This methodology involves extraction of isoprenoids from cultured cells followed by enzymatic conjugation of GPP to a fluorescent dansylated-peptide via farnesyl transferase and quantification with high-performance liquid chromatography (HPLC). The lower limit of detection of GPP is 5 pg, or 0.015 pmol. Basal levels of GPP were determined in three human multiple myeloma cell lines (RPMI-8226, U266, H929). Treatment of cells with inhibitors of the isoprenoid biosynthetic pathway results in marked changes in GPP levels: the HMG-CoA reductase inhibitor lovastatin decreases GPP levels by over 50%, while the FPP synthase inhibitor zoledronic acid increases GPP levels 16- to 107-fold. This method also allows for the simultaneous measurement of GPP, FPP, and GGPP, thus leading to improved understanding of the pathway in a multitude of biological systems. Furthermore, as drugs targeting this pathway are developed, their biological activity can be more directly linked to effects on isoprenoid levels.

摘要

香叶基二磷酸(GPP)是一种含10个碳原子的类异戊二烯,是类异戊二烯生物合成途径中的关键中间体。该途径除了导致甾醇合成外,还会合成法尼基二磷酸(FPP)和香叶基香叶基二磷酸(GGPP),它们作为蛋白质异戊烯化反应的底物。此前在哺乳动物细胞中未检测到GPP的基础水平。在此,我们提出了一种新颖、灵敏的非放射性方法,可用于测量哺乳动物细胞中的GPP。该方法包括从培养细胞中提取类异戊二烯,然后通过法尼基转移酶将GPP与荧光丹磺酰化肽进行酶促偶联,并通过高效液相色谱(HPLC)进行定量。GPP的检测下限为5 pg,即0.015 pmol。在三种人多发性骨髓瘤细胞系(RPMI - 8226、U266、H929)中测定了GPP的基础水平。用类异戊二烯生物合成途径抑制剂处理细胞会导致GPP水平发生显著变化:HMG - CoA还原酶抑制剂洛伐他汀使GPP水平降低超过50%,而FPP合酶抑制剂唑来膦酸使GPP水平升高16至107倍。该方法还允许同时测量GPP、FPP和GGPP,从而有助于在众多生物系统中更好地理解该途径。此外,随着针对该途径的药物不断开发,它们的生物活性可以更直接地与对类异戊二烯水平的影响联系起来。

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本文引用的文献

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Peripheral blood monocytes are responsible for gammadelta T cell activation induced by zoledronic acid through accumulation of IPP/DMAPP.外周血单核细胞通过IPP/DMAPP的积累,负责唑来膦酸诱导的γδ T细胞活化。
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