The engineering of microbial rhodopsins with enhanced fluorescence is of great importance in the expanding field of optogenetics. Here we report the discovery of two mutants (W76S/Y179F and L83Q) of a sensory rhodopsin from the cyanobacterium Anabaena PCC7120 with opposite fluorescence behavior. In fact, while W76S/Y179F displays, with respect to the wild-type protein, a nearly ten-fold increase in red-light emission, the second is not emissive. Thus, the W76S/Y179F, L83Q pair offers an unprecedented opportunity for the investigation of fluorescence enhancement in microbial rhodopsins, which is pursued by combining transient absorption spectroscopy and multi-configurational quantum chemistry. The results of such an investigation point to an isomerization-blocking electronic effect as the direct cause of instantaneous (sub-picosecond) fluorescence enhancement.
Marín, M.D.C., Agathangelou, D., Orozco-Gonzalez, Y., Valentini, A., Kato, Y., Abe-Yoshizumi, R., et al. (2019). Fluorescence enhancement of a microbial rhodopsin via electronic reprogramming. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 141(1), 262-271 [10.1021/jacs.8b09311].
Fluorescence enhancement of a microbial rhodopsin via electronic reprogramming
Marín, María Del Carmen;Valentini, Alessio;Olivucci, Massimo
2019-01-01
Abstract
The engineering of microbial rhodopsins with enhanced fluorescence is of great importance in the expanding field of optogenetics. Here we report the discovery of two mutants (W76S/Y179F and L83Q) of a sensory rhodopsin from the cyanobacterium Anabaena PCC7120 with opposite fluorescence behavior. In fact, while W76S/Y179F displays, with respect to the wild-type protein, a nearly ten-fold increase in red-light emission, the second is not emissive. Thus, the W76S/Y179F, L83Q pair offers an unprecedented opportunity for the investigation of fluorescence enhancement in microbial rhodopsins, which is pursued by combining transient absorption spectroscopy and multi-configurational quantum chemistry. The results of such an investigation point to an isomerization-blocking electronic effect as the direct cause of instantaneous (sub-picosecond) fluorescence enhancement.File | Dimensione | Formato | |
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https://hdl.handle.net/11365/1067044