학술논문

Human infrared vision is triggered by two-photon chromophore isomerization.
Document Type
article
Source
Proceedings of the National Academy of Sciences of USA. 111(50)
Subject
multiscale modeling
rhodopsin
transretinal electrophysiology
two-photon absorption
visual pigment
Absorption
Radiation
Adult
Animals
Cattle
Computer Simulation
Electroretinography
Female
Humans
Infrared Rays
Isomerism
Lasers
Male
Mice
Photons
Photoreceptor Cells
Vertebrate
Psychophysics
Rhodopsin
Vision
Ocular
Language
Abstract
Vision relies on photoactivation of visual pigments in rod and cone photoreceptor cells of the retina. The human eye structure and the absorption spectra of pigments limit our visual perception of light. Our visual perception is most responsive to stimulating light in the 400- to 720-nm (visible) range. First, we demonstrate by psychophysical experiments that humans can perceive infrared laser emission as visible light. Moreover, we show that mammalian photoreceptors can be directly activated by near infrared light with a sensitivity that paradoxically increases at wavelengths above 900 nm, and display quadratic dependence on laser power, indicating a nonlinear optical process. Biochemical experiments with rhodopsin, cone visual pigments, and a chromophore model compound 11-cis-retinyl-propylamine Schiff base demonstrate the direct isomerization of visual chromophore by a two-photon chromophore isomerization. Indeed, quantum mechanics modeling indicates the feasibility of this mechanism. Together, these findings clearly show that human visual perception of near infrared light occurs by two-photon isomerization of visual pigments.