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通过活细胞中的高通量时间分辨荧光共振能量转移发现酶调节剂。

Discovery of enzyme modulators via high-throughput time-resolved FRET in living cells.

作者信息

Gruber Simon J, Cornea Razvan L, Li Ji, Peterson Kurt C, Schaaf Tory M, Gillispie Gregory D, Dahl Russell, Zsebo Krisztina M, Robia Seth L, Thomas David D

机构信息

1Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Minneapolis, MN, USA.

出版信息

J Biomol Screen. 2014 Feb;19(2):215-22. doi: 10.1177/1087057113510740.

Abstract

We have used a "two-color" SERCA (sarco/endoplasmic reticulum calcium ATPase) biosensor and a unique high-throughput fluorescence lifetime plate reader (FLT-PR) to develop a high-precision live-cell assay designed to screen for small molecules that perturb SERCA structure. A SERCA construct, in which red fluorescent protein (RFP) was fused to the N terminus and green fluorescent protein (GFP) to an interior loop, was stably expressed in an HEK cell line that grows in monolayer or suspension. Fluorescence resonance energy transfer (FRET) from GFP to RFP was measured in the FLT-PR, which increases precision 30-fold over intensity-based plate readers without sacrificing throughput. FRET was highly sensitive to known SERCA modulators. We screened a small chemical library and identified 10 compounds that significantly affected two-color SERCA FLT. Three of these compounds reproducibly lowered FRET and inhibited SERCA in a dose-dependent manner. This assay is ready for large-scale HTS campaigns and is adaptable to many other targets.

摘要

我们使用了一种“双色”肌浆网/内质网钙ATP酶(SERCA)生物传感器和一台独特的高通量荧光寿命酶标仪(FLT-PR),开发了一种高精度活细胞检测方法,用于筛选能够干扰SERCA结构的小分子。一种SERCA构建体,其中红色荧光蛋白(RFP)融合到N端,绿色荧光蛋白(GFP)融合到一个内环,在单层或悬浮生长的HEK细胞系中稳定表达。在FLT-PR中测量从GFP到RFP的荧光共振能量转移(FRET),与基于强度的酶标仪相比,其精度提高了30倍,同时不牺牲通量。FRET对已知的SERCA调节剂高度敏感。我们筛选了一个小型化学文库,鉴定出10种对双色SERCA FLT有显著影响的化合物。其中三种化合物可重复性地降低FRET,并以剂量依赖的方式抑制SERCA。该检测方法已准备好用于大规模的高通量筛选活动,并且适用于许多其他靶点。

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