Retinene

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

The Retinenes (Retinene₁ and Retinene₂) are chemical derivatives of the dietary supplement vitamin A (see retinol) formed through oxidation reactions.

Retinene₁ is better known as retinaldehyde or simply retinal and is fundamental in the transduction of light into visual signals in the photoreceptor level of the retina (known as the visual cycle). Retinene₂ is more formally known as dehydroretinaldehyde.

The energy of impinging photons will convert retinaldehyde from an 11-cis isomer into an all-trans form. In the retina, this conversion induces a conformational change in the surrounding photopsin protein pigment, leading to signaling through the G protein transducin. Retinaldehyde also forms a part of bacteriorhodopsin, a light-induced proton pump found in some archaea.

Experimentally, it is possible to replace 11-cis retinaldehyde by perfusing retinal tissue preparations with retinaldehyde derivatives. Selective modification of the retinaldehyde structure, particularly the density of electrons in the π-orbitals, can lead to insights into the interaction between the retinaldehyde moiety and the surrounding pigment protein.

See also

• Retinal
• Visual cycle

de:Retinal