Simple Method for Studying in Vitro Protein-Protein Interactions Based on Protein Complementation and Its Application in Drug Screening Targeting Bacterial Transcription

被引:17
|
作者
Tsang, Tsz Fung [1 ]
Qiu, Yangyi [2 ,3 ,4 ]
Lin, Lin [1 ]
Ye, Jiqing [2 ,3 ,4 ]
Ma, Cong [2 ,3 ,4 ]
Yang, Xiao [1 ]
机构
[1] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Microbiol, Shatin, 30-32 Ngan Shing St, Hong Kong, Peoples R China
[2] Hong Kong Polytech Univ, Shenzhen Res Inst, 18 Yue Xing Ist Rd, Shenzhen 518057, Guangdong, Peoples R China
[3] Hong Kong Polytech Univ, State Key Lab Chem Biol & Drug Discovery, Kowloon, 11 Yuk Choi Rd, Hong Kong, Peoples R China
[4] Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Kowloon, 11 Yuk Choi Rd, Hong Kong, Peoples R China
来源
ACS INFECTIOUS DISEASES | 2019年 / 5卷 / 04期
关键词
protein-protein interactions; protein complementation assay; in vitro drug screening; bacterial transcription; antimicrobial agent; RNA-POLYMERASE; INHIBITORS; DISCOVERY; BINDING; COMPLEX; NUSB;
D O I
10.1021/acsinfecdis.9b00020
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Protein-protein interactions (PPIs) underpin essential cellular processes of all organisms and are increasingly considered as drug targets. A number of techniques have been established to study PPIs; however, development of a simple and cost-effective method for in vitro high throughput screening of PPI inhibitors is still in demand or desirable. We report herein a simple method based on protein complementation for the in vitro study of PPIs, as well as screening of inhibitors against the PPI of interest. We have validated this system utilizing bacterial transcription factors NusB and NusE. Three derivatives of an inhibitor targeting the NusB-NusE interaction were synthesized and characterized with the system, which showed specific inhibition and antimicrobial activities. We have further confirmed the system with the RNA polymerase-sigma interaction and an inhibitor. This system is expected to be suitable for more extensive high throughput screening of large chemical libraries. Additionally, our vector system can be easily adapted to study other PPI pairs, followed by inhibitor screening for hit identification in the application of early stage drug discovery.
引用
收藏
页码:521 / 527
页数:13
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