Sandbox Reserved 1451

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This Sandbox is Reserved from Jan 22 through May 22, 2018 for use in the course Biochemistry II taught by Jason Telford at the Maryville University, St. Louis, Missouri, USA. This reservation includes Sandbox Reserved 1446 through Sandbox Reserved 1455.

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<Structure Section load='1jfp' size='340' side='right' scene= caption='Bovine rhodopsin complex with retinal (PDB code 1jfp)'>

Rhodopsin

Rhodopsin is a member of the G-protein coupled receptor (GPCR) family. Rhodopsin is the common GPCR structure used to understand functionality of G-protein coupled receptors. Rhodopsin is commonly found in the photoreceptors in the retina, specifically in the rod photoreceptors and become activated by photons of light. Rhodopsin contains a chromophore (compound that absorbs light), specifically 11-cis-retinal, which when active recruites G proteins to transmit a signaling cascade in neural impulses to the gray matter of the occipital lobe. Once the receptor has been activated, a new rhodopsin needs to be regenerated. Rhodopsin is located in the rod outer segment (ROS) which consists of stacked disks enclosed by a membrane. The entire family of GPCR’s have the common structure of seven alpha-helices across membranes. Rhodopsin’s structure changes upon photoactivation. The sixth helix bends away from the seventh creating a pocket that allows for binding of a G protein. A salt bridge covers this pocket until the helices shift away from one another. Once the G protein has bound then the signal can be transmitted to the occipital lobe. Over 120 point mutations to rhodopsin have been identified which can lead to night blindness and more several visual problems.

Function

Rhodopsin performs two functions. One function is to bind retinal. Another function is to function as a G protein-coupled receptor. Rhodopsin is a protein that is essential for vision, especially in dim light. The photoreceptors in the retina that contain rhodopsin are rods. Rhodopsin is attached to 11-cis retinal which becomes excited by a photon of light. This excitation activates rhodopsin and leads to depolarizing of neurons. The depolarizing of neurons is how the image is transmitted to the brain. (https://ghr.nlm.nih.gov/gene/RHO#)

Disease

Mutations to rhodopsin can lead to stationary night blindness or retinitis pigmentosa.

Autosomal Dominant Congenial Stationary Night Blindness Stationary night blindness is an autosomal dominant disease that causes a loss of vision in dim light. The mutation to rhodopsin causes the protein to be constantly activated. Since the protein is continuously activated without any photon of light, the brain continues to receive stimulation from the photoreceptors. The brain begins to ignore the visual stimulation from the rods, therefore leading to night blindness.

Retinitis Pigmentosa Retinitis pigmentosa is also an autosomal dominant disorder, but can also be recessive in rare circumstances. A mutation that affect rhodopsin that cause retinitis pigmentosa result in a misfolding or transportation of the protein. Another mutation to rhodopsin can affect the activation of the protein in response to light. These mutations can lead to apoptosis of rods in the retina. Without rods to perceive dim light, night blindness results. (https://ghr.nlm.nih.gov/gene/RHO#)

Relevance

Up until 2007, rhodopsin was the only GPCR that had a high-resolution crystal structure and was the basis for other GPCR structures. (https://www.ncbi.nlm.nih.gov/pubmed/24041646)

Structural highlights

This is rhodopsin without 11-cis retinal bound.Rhodopsin

This is 11-cis retinal that rhodopsin binds.11-cis retinal

This is rhodopsin with 11-cis retinal bound.Rhodopsin bound 11-cis retinal

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