Directed Evolution of a Bright Near-Infrared Fluorescent Rhodopsin Using a Synthetic Chromophore

• Published in: Cell chemical biology Vol. 24; no. 3; p. 415
• Main Authors: Herwig, Lukas, Rice, Austin J, Bedbrook, Claire N, Zhang, Ruijie K, Lignell, Antti, Cahn, Jackson K B, Renata, Hans, Dodani, Sheel C, Cho, Inha, Cai, Long, Gradinaru, Viviana, Arnold, Frances H
• Format: Journal Article
• Language: English
• Published: United States 16-03-2017
• Subjects: Binding Sites; Directed Molecular Evolution; Escherichia coli - metabolism; Hydrogen-Ion Concentration; Isomerism; Kinetics; Microscopy, Fluorescence; Molecular Docking Simulation; Mutagenesis, Site-Directed; Protein Structure, Tertiary; Retinaldehyde - chemical synthesis; Retinaldehyde - chemistry; Retinaldehyde - metabolism; Rhodopsin - chemistry; Rhodopsin - genetics; Rhodopsin - metabolism; Spectroscopy, Near-Infrared; near-infrared fluorescence; synthetic chromophore substitution; protein engineering; Archaerhodopsin; live-cell imaging; directed evolution
• ISSN: 2451-9456
• DOI: 10.1016/j.chembiol.2017.02.008

By engineering a microbial rhodopsin, Archaerhodopsin-3 (Arch), to bind a synthetic chromophore, merocyanine retinal, in place of the natural chromophore all-trans-retinal (ATR), we generated a protein with exceptionally bright and unprecedentedly red-shifted near-infrared (NIR) fluorescence. We show that chromophore substitution generates a fluorescent Arch complex with a 200-nm bathochromic excitation shift relative to ATR-bound wild-type Arch and an emission maximum at 772 nm. Directed evolution of this complex produced variants with pH-sensitive NIR fluorescence and molecular brightness 8.5-fold greater than the brightest ATR-bound Arch variant. The resulting proteins are well suited to bacterial imaging; expression and stability have not been optimized for mammalian cell imaging. By targeting both the protein and its chromophore, we overcome inherent challenges associated with engineering bright NIR fluorescence into Archaerhodopsin. This work demonstrates an efficient strategy for engineering non-natural, tailored properties into microbial opsins, properties relevant for imaging and interrogating biological systems.