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实时监测法呢醇磷酸焦磷酸酶合成反应中肽链延伸的荧光底物类似物。

Fluorescent substrate analog for monitoring chain elongation by undecaprenyl pyrophosphate synthase in real time.

机构信息

Institute of Biological Chemistry, Academia Sinica, Taipei 115, Taiwan, ROC.

出版信息

Anal Biochem. 2011 Oct 1;417(1):136-41. doi: 10.1016/j.ab.2011.05.043. Epub 2011 Jun 7.

Abstract

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.

摘要

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。

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