A NanoBiT assay to monitor membrane proteins trafficking for drug discovery and drug development

  • Reyes-Alcaraz, Arfaxad; 
  • Lucero Garcia-Rojas, Emilio Y.; 
  • Merlinsky, Elizabeth A.; 
  • Seong, Jae Young; 
  • Bond, Richard A.; 
  • 외 1명
Citations

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20

초록

Internalization of membrane proteins plays a key role in many physiological functions; however, highly sensitive and versatile technologies are lacking to study such processes in real-time living systems. Here we describe an assay based on bioluminescence able to quantify membrane receptor trafficking for a wide variety of internalization mechanisms such as GPCR internalization/recycling, antibody-mediated internalization, and SARS-CoV2 viral infection. This study represents an alternative drug discovery tool to accelerate the drug development for a wide range of physiological processes, such as cancer, neurological, cardiopulmonary, metabolic, and infectious diseases including COVID-19. Membrane protein trafficking is monitored using split nanoluciferase. Receptor internalization leads to complementation on the early endosome and a bioluminescent response, and is applied to receptor internalization/recycling, antibody-mediated internalization and SARS-CoV2 entry.

키워드

RECEPTOR INTERNALIZATION; COMPOUND HETEROZYGOSITY; IN-SITU; MUTATIONS; CCR5
제목
A NanoBiT assay to monitor membrane proteins trafficking for drug discovery and drug development
저자
Reyes-Alcaraz, Arfaxad; Lucero Garcia-Rojas, Emilio Y.; Merlinsky, Elizabeth A.; Seong, Jae Young; Bond, Richard A.; McConnell, Bradley K.
DOI
10.1038/s42003-022-03163-9
발행일
2022-03-08
유형
Article
저널명
Communications Biology
권
5
호
1