Single-molecule FRET and conformational analysis of beta-arrestin-1 through genetic code expansion and a Se-click reaction. Issue 26 (9th June 2021)

• Record Type: Journal Article
• Authors: Han, Ming-Jie; He, Qing-tao; Yang, Mengyi; Chen, Chao; Yao, Yirong; Liu, Xiaohong; Wang, Yuchuan; Zhu, Zhong-liang; Zhu, Kong-kai; Qu, Changxiu; Yang, Fan; Hu, Cheng; Guo, Xuzhen; Zhang, Dawei; Chen, Chunlai; Sun, Jin-peng; Wang, Jiangyun
• Is Part Of: Chemical science. Volume 12:Issue 26(2021)
• Page Start: 9114
• Page End: 9123
• Publication Date: 2021-06-09
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d1sc02653d
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : A facile bioconjugation reaction for site-specific protein modification was developed for smFRET measurement, which detected the subtle but important conformational change of the β-arrestin/GPCR complex for the first time. Abstract : Single-molecule Förster resonance energy transfer (smFRET) is a powerful tool for investigating the dynamic properties of biomacromolecules. However, the success of protein smFRET relies on the precise and efficient labeling of two or more fluorophores on the protein of interest (POI), which has remained highly challenging, particularly for large membrane protein complexes. Here, we demonstrate the site-selective incorporation of a novel unnatural amino acid (2-amino-3-(4-hydroselenophenyl) propanoic acid, SeF) through genetic expansion followed by a Se-click reaction to conjugate the Bodipy593 fluorophore on calmodulin (CaM) and β-arrestin-1 (βarr1). Using this strategy, we monitored the subtle but functionally important conformational change of βarr1 upon activation by the G-protein coupled receptor (GPCR) through smFRET for the first time. Our new method has broad applications for the site-specific labeling and smFRET measurement of membrane protein complexes, and the elucidation of their dynamic properties such as transducer protein selection.