Luminescence Energy Transfer-Based Screening and Target Engagement Approaches for Chemical Biology and Drug Discovery

被引:7
|
作者
Cho, Eun Jeong [1 ]
Dalby, Kevin N. [1 ]
机构
[1] Univ Texas Austin, Coll Pharm, Div Chem Biol & Med Chem, Targeted Therapeut Drug Discovery & Dev Program, 107 W Dean Keaton St,STOP C0850,BME 6-202B, Austin, TX 78712 USA
关键词
luminescence; NanoBRET; AlphaScreen; AlphaLISA; target engagement; high-throughput screen; LIGAND-BINDING; PROTEIN; ASSAYS; IDENTIFICATION; TECHNOLOGY; PLATFORM; BRET; INHIBITOR; NANOLUC; PROBES;
D O I
10.1177/24725552211036056
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Luminescence is characterized by the spontaneous emission of light resulting from either chemical or biological reactions. Because of their high sensitivity, reduced background interference, and applicability to numerous situations, luminescence-based assay strategies play an essential role in early-stage drug discovery. Newer developments in luminescence-based technologies have dramatically affected the ability of researchers to investigate molecular binding events. At the forefront of these developments are the nano bioluminescence resonance energy transfer (NanoBRET) and amplified luminescent proximity homogeneous assay (Alpha) technologies. These technologies have opened up numerous possibilities for analyzing the molecular biophysical properties of complexes in environments such as cell lysates. Moreover, NanoBRET enables the validation and quantitation of the interactions between therapeutic targets and small molecules in live cells, representing an essential benchmark for preclinical drug discovery. Both techniques involve proximity-based luminescence energy transfer, in which excited-state energy is transferred from a donor to an acceptor, where the efficiency of transfer depends on proximity. Both approaches can be applied to high-throughput compound screening in biological samples, with the NanoBRET assay providing opportunities for live-cell screening. Representative applications of both technologies for assessing physical interactions and associated challenges are discussed.
引用
收藏
页码:984 / 994
页数:11
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