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MECHANISMS OF VISION Jiří Wilhelm
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Page 1: MECHANISMS OF VISION Jiří Wilhelm. Rhodopsin.

MECHANISMS OF VISION

Jiří Wilhelm

Page 2: MECHANISMS OF VISION Jiří Wilhelm. Rhodopsin.

Rhodopsin

Page 3: MECHANISMS OF VISION Jiří Wilhelm. Rhodopsin.
Page 4: MECHANISMS OF VISION Jiří Wilhelm. Rhodopsin.
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One photon corresponds to 100 000 cGMP hydrolyzed

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Human retina contains about100 milion rods and3 milion cones.Maximum light absorption ofrhodopsin in rods is around500 nm3 classes of cones absorb at440 nm530 nm570 nm

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DAMPING OF THE RESPONSE

In daylight all rods are fully activated, thus in order to distinguishcontrast the response must be dampened.

Downregulation of signaling by G proteins is generally producedby RGS proteins (Regulators of G protein Signaling).

In retina, RGS proteins are represented by Phosducin.In slight contrast to other RGS proteins Phosducin preferes-subunits of the G protein over -subunit. Binding both - and- subunits in light-adapted rods blocks the formation of complex and reduces the turnover of the G-protein cycle.

In the dark-adapted eye Phosducin is inactive.

Page 11: MECHANISMS OF VISION Jiří Wilhelm. Rhodopsin.

Another damping protein

GARP, glutamic-acid-richprotein is contained in rodsbut not cones receptors.

PDE – phosphodiesteraseABCR – Retinal ATP-binding ABC transporter

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RESENSITIZATION OF VISUAL RESPONSE

The general step consists in G-protein dephosphorylation. In retinait is regulated by calcium and recoverin, a calcium-regulated protein.The phosphatase dephosphorylating rhodopsin is typical serine/threonine phosphatase.

The dissociated all-trans-retinal is reduced to all-trans-retinol, thenit is transfered to the neighboring retinal pigment epithelial cells,where reisomerisation and reoxidation recycles 11-cis-retinal. That isreturned to rod and cone outer segments, where it recombines withopsin to form rhodopsin.