Protonation states of highly conserved carboxylic acids in NeoR

Abstract

Neorhodopsin (NeoR), an enzymerhodopsin, has unique molecular properties. NeoR absorbs near-infrared light whose λ_max is located at 690-700 nm. Upon light absorption, NeoR is photoisomerized into the 7-cis form with low quantum yield. Unique color-tuning and photoreaction mechanism of NeoR is owing to the residues surrounding the all-trans retinal chromophore. In NeoR, three carboxylates, E136, D140, and E262, constitute a counterion triad near the retinal Schiff base, and E141 is located near the β-ionone ring. Despite recent experimental and theoretical studies, protonation states of the highly conserved four carboxylates have never been experimentally determined. In this study, we performed comprehensive mutation analysis of NeoR by UV-visible and FTIR spectroscopy. We prepared E136Q, D140N, E141Q, and E262Q mutants of an NeoR. Among four mutants, only E262Q did not form a pigment, suggesting that E262 is the principal Schiff base counterion. Light-induced FTIR spectroscopy detected two bands of protonated carboxylic acids, and vibrational bands were identified as protonated D140 and E141. Hydrogen bond of D140 is strong in NeoR, which is further strengthened upon photoisomerization into the 7-cis form. The Schiff base is the possible hydrogen-bonding partner of D140. Hydrogen bond of E141 is very weak in NeoR, but E141 newly forms a hydrogen bond upon 7-cis isomerization. Protonation states of E136 and E262 were not determined conclusively, whereas the present FTIR study suggests that one negative charge is delocalized at E136 and E262 that contributes to unusual spectral red-shift in NeoR. Four carboxylates near the retinal chromophore in NeoR play their own roles in unique color-tuning and photoreaction mechanism.

Caption of Graphical Abstract

Neorhodopsin (NeoR), an enzymerhodopsin, has λmax at 690–700 nm, and four carboxylic acids near the retinal chromophore play important roles for the unique spectral red-shift. This study aimed at revealing their protonation states in combination of D/N or E/Q mutation, and FTIR spectroscopy. In the resting state of NeoR, E141 and D140 are protonated, whereas one negative charge is delocalized at E136 and E262 that contributes to unusual spectral red-shift in NeoR. In the UV-absorbing photoproduct state with 7-cis retinal, the protonation states of these residues remain unchanged; however, the broadened peak of E141 indicates increased structural fluctuations.