Retinal Isomerization

Retinal isomerization is the light-triggered change in the shape of retinal, a vitamin A-derived chromophore bound to opsin proteins in photoreceptor cells, and it initiates visual signaling. When a photon is absorbed, 11-cis-retinal rapidly converts to all-trans-retinal, altering the conformation of rhodopsin and activating the phototransduction cascade that changes the membrane potential of rods and cones. Enzymatic reactions then convert retinal back to its 11-cis form through the visual cycle, allowing photoreceptors to respond repeatedly. Studying this process helps explain normal vision and the molecular basis of visual disorders involving photopigment function or chromophore regeneration.

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Education

JoVE Core - Chemistry

Structural Isomerism

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2020

Isomerism in Complexes Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers. Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can be...

Isomerism

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2023

Isomers are molecules with the same molecular formula but different structural arrangements. Isomers can be further classified into constitutional isomers and stereoisomers. Constitutional isomers differ in the connectivity of their constituent atoms. For example, 2-butanol and diethyl ether are constitutional isomers, as they have the same chemical formula, C4H10O, but differ in the connectivity of the carbon and oxygen atoms. Constitutional isomers have different physical and chemical...

Isomerism in Alkenes

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2025

Alkenes like 1-butene and 2-butene exhibit constitutional isomerism, as they differ in the position of the double bond. Further, 2-butene exhibits stereoisomerism and exists as two distinct compounds differing in spatial arrangement. An isomer is called cis-2-butene when the methyl groups are on the same side of the double bond, and the other stereoisomer, in which methyl groups are on the opposite side of the double bond, is called trans-2-butene. The cis and trans stereoisomers are not...

Disubstituted Cyclohexanes: cis-trans Isomerism

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2023

Depending upon the different spatial orientation of the substituents, the disubstituted cycloalkanes exhibit two types of stereoisomers. The cis isomers have the substituents on the same side of the ring, whereas the trans isomers have the substituents on the opposite sides. These stereoisomers exhibit different physical properties and cannot be interconverted without breaking the carbon-carbon bonds. In cyclohexane, the substituents can occupy different positions generating distinct isomers.

Research

JoVE EoE - Viral Growth and Techniques

Preparation of Mouse Retinal Cryosections to Assess Retinal Permeability to Adeno-Associated Virus

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2026

Source: Vacca, O., et al. Using Adeno-associated Virus as a Tool to Study Retinal Barriers in Disease. J. Vis. Exp. (2015)This video demonstrates the step-by-step procedure for preparing mouse retinal cryosections to visualize adeno-associated virus permeability across disrupted retinal barriers.

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