Institute of Biological Chemistry, Academia Sinica, Taipei 115, Taiwan, ROC.
Anal Biochem. 2011 Oct 1;417(1):136-41. doi: 10.1016/j.ab.2011.05.043. Epub 2011 Jun 7.
Farnesyl pyrophosphate (FPP) is a common substrate for a variety of prenyltransferases for synthesizing isoprenoid compounds. In this study, (2E,6E)-8-O-(N-methyl-2-aminobenzoyl)-3,7-dimethyl-2,6-octandien-1-pyrophosphate (MANT-O-GPP), a fluorescent analog of FPP, was synthesized and demonstrated as a satisfactory substrate for Escherichia coli undecaprenyl pyrophosphate synthase (UPPS) with a K(m) of 1.5 μM and a k(cat) of 1.2s(-1) based on [(14)C]IPP consumption. Interesting, we found that its emission fluorescence intensity at 420 nm increased remarkably during chain elongation, thereby useful for real-time monitoring kinetics of UPPS to yield a K(m) of 1.1 μM and a k(cat) of 1.0 s(-1), consistent with those measured using radiolabeled substrate. Using this assay, the IC(50) of a known UPPS inhibitor farnesyl thiopyrophosphate (FsPP) was confirmed. Our studies provide a convenient and environmentally friendly alternative for kinetics and inhibition studies on UPPS drug target.
法呢基焦磷酸(FPP)是各种异戊烯基转移酶合成类异戊二烯化合物的共同底物。在本研究中,合成了荧光类似物(2E,6E)-8-O-(N-甲基-2-氨基苯甲酰基)-3,7-二甲基-2,6-辛二烯-1-焦磷酸(MANT-O-GPP),并证明其是大肠杆菌十一碳烯焦磷酸合酶(UPPS)的满意底物,其 K(m)为 1.5 μM,k(cat)为 1.2s(-1),基于 [(14)C]IPP 的消耗。有趣的是,我们发现其在链延伸过程中 420nm 处的发射荧光强度显著增加,因此可用于实时监测 UPPS 的动力学,得到 K(m)为 1.1 μM,k(cat)为 1.0 s(-1),与使用放射性标记底物测量的值一致。使用该测定法,确认了已知 UPPS 抑制剂法尼基硫代焦磷酸(FsPP)的 IC(50)。我们的研究为 UPPS 药物靶点的动力学和抑制研究提供了一种方便且环保的替代方法。