Artificial color tuning of firefly luminescence: Theoretical mutation by tuning electrostatic interactions between protein and luciferin

Electrostatic interactions between firefly oxyluciferin and the surrounding proteins were analyzed, and the amino acids important for controlling emission energy were identified. We propose Arg223Ala, Glu344Ala, and Asp422Ala mutations in firefly oxyluciferase of Photinuspyralis, which artificially change the luminescence color by tuning the electrostatic effect from the luciferase proteins. In the theoretical mutation simulation, the emission energy of the triple mutant was estimated to be 2.05 eV (602 nm, reddish-orange), which is 0.18 eV lower than that of the wild type (2.23 eV, 557 nm, yellow-green). For calculating the emission energies, we used the symmetry-adapted cluster-configuration interaction (SAC-CI) method.

Arg223Ala, Glu344Ala, and Asp422Ala mutations in the firefly oxyluciferase of Photinuspyralis, which could change the luminescence color into reddish-orange.72