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HTRF:一种为药物发现量身定制的技术——理论层面与近期应用综述

HTRF: A technology tailored for drug discovery - a review of theoretical aspects and recent applications.

作者信息

Degorce François, Card Amy, Soh Sharon, Trinquet Eric, Knapik Glenn P, Xie Bing

机构信息

Cisbio Bioassays, 30204 Bagnols-Sur-Cèze, France.

出版信息

Curr Chem Genomics. 2009 May 28;3:22-32. doi: 10.2174/1875397300903010022.

Abstract

HTRF (Homogeneous Time Resolved Fluorescence) is the most frequently used generic assay technology to measure analytes in a homogenous format, which is the ideal platform used for drug target studies in high-throughput screening (HTS). This technology combines fluorescence resonance energy transfer technology (FRET) with time-resolved measurement (TR). In TR-FRET assays, a signal is generated through fluorescent resonance energy transfer between a donor and an acceptor molecule when in close proximity to each other. Buffer and media interference is dramatically reduced by dual-wavelength detection, and the final signal is proportional to the extent of product formation. The HTRF assay is usually sensitive and robust that can be miniaturized into the 384 and 1536-well plate formats. This assay technology has been applied to many antibody-based assays including GPCR signaling (cAMP and IP-One), kinases, cytokines and biomarkers, bioprocess (antibody and protein production), as well as the assays for protein-protein, proteinpeptide, and protein-DNA/RNA interactions.Since its introduction to the drug-screening world over ten years ago, researchers have used HTRF to expedite the study of GPCRs, kinases, new biomarkers, protein-protein interactions, and other targets of interest. HTRF has also been utilized as an alternative method for bioprocess monitoring. The first-generation HTRF technology, which uses Europium cryptate as a fluorescence donor to monitor reactions between biomolecules, was extended in 2008 through the introduction of a second-generation donor, Terbium cryptate (Tb), enhancing screening performance. Terbium cryptate possesses different photophysical properties compared to Europium, including increased quantum yield and a higher molar extinction coefficient. In addition to being compatible with the same acceptor fluorophors used with Europium, it can serve as a donor fluorophore to green-emitting fluors because it has multiple emission peaks including one at 490 nm. Moreover, all Terbium HTRF assays can be read on the same HTRF-compatible instruments as Europium HTRF assays.Overall, HTRF is a highly sensitive, robust technology for the detection of molecular interactions in vitro and is widely used for primary and secondary screening phases of drug development. This review addresses the general principles of HTRF and its current applications in drug discovery.

摘要

均相时间分辨荧光(HTRF)是测量均相体系中分析物时最常用的通用检测技术,是用于高通量筛选(HTS)中药物靶点研究的理想平台。该技术将荧光共振能量转移技术(FRET)与时间分辨测量(TR)相结合。在时间分辨荧光共振能量转移(TR-FRET)检测中,当供体分子和受体分子彼此靠近时,通过它们之间的荧光共振能量转移产生信号。双波长检测显著降低了缓冲液和介质的干扰,最终信号与产物形成的程度成正比。HTRF检测通常灵敏且稳健,可小型化至384孔板和1536孔板形式。该检测技术已应用于许多基于抗体的检测,包括GPCR信号传导(cAMP和IP-One)、激酶、细胞因子和生物标志物、生物过程(抗体和蛋白质生产),以及蛋白质-蛋白质、蛋白质-肽和蛋白质-DNA/RNA相互作用的检测。自十多年前引入药物筛选领域以来,研究人员一直使用HTRF来加速GPCR、激酶、新生物标志物、蛋白质-蛋白质相互作用及其他感兴趣靶点的研究。HTRF也已被用作生物过程监测的替代方法。第一代HTRF技术使用铕穴状配合物作为荧光供体来监测生物分子之间的反应,2008年通过引入第二代供体铽穴状配合物(Tb)得以扩展,提高了筛选性能。铽穴状配合物与铕相比具有不同的光物理性质,包括更高的量子产率和更高的摩尔消光系数。除了与铕使用的相同受体荧光团兼容外,它还可以作为绿色发射荧光团的供体荧光团,因为它有多个发射峰,包括一个在490nm处的峰。此外,所有铽HTRF检测都可以在与铕HTRF检测兼容的相同仪器上读取。总体而言,HTRF是一种用于体外分子相互作用检测的高度灵敏、稳健的技术,广泛应用于药物开发的初级和次级筛选阶段。本综述阐述了HTRF的一般原理及其在药物发现中的当前应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01eb/2802762/c52ada34ea46/TOCHGENJ-3-22_F1.jpg

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