photoreception : mechanisms of transduction, and non-vertebrate eyes

15
photoreception: mechanisms of transduction, and non-vertebrate eyes The energy detected:

description

photoreception : mechanisms of transduction, and non-vertebrate eyes. The energy detected:. The game plan. Who does it… or where do you find sensory organs containing retinal / rhodopsin?. - PowerPoint PPT Presentation

Transcript of photoreception : mechanisms of transduction, and non-vertebrate eyes

Page 1: photoreception : mechanisms of transduction, and non-vertebrate eyes

photoreception: mechanisms of transduction, and non-vertebrate eyes

The energy detected:

Page 2: photoreception : mechanisms of transduction, and non-vertebrate eyes
Page 3: photoreception : mechanisms of transduction, and non-vertebrate eyes

The game plan

Page 4: photoreception : mechanisms of transduction, and non-vertebrate eyes

Who does it… or where do you find sensory organs containing retinal / rhodopsin?

Note: there is also Bacteriorhodopsin – similar to rhodopsin of all other organisms - but not used for photo-sensory detection. Rather it is a mechanism like photosynthesis to drive uni-directional ion transport for energy generation.

Page 5: photoreception : mechanisms of transduction, and non-vertebrate eyes

Retinal as held in protein opsin

Page 6: photoreception : mechanisms of transduction, and non-vertebrate eyes
Page 7: photoreception : mechanisms of transduction, and non-vertebrate eyes

Retinal in opsin pocket (four different 11-cis isomers)

From: Jang et al, Mechanism of rhodopsin activation as examined with ring contstrained retinal analogs and the crystal structure of the ground state protein. J. Biol. Chem. (2001) 276:26148-26153

Page 8: photoreception : mechanisms of transduction, and non-vertebrate eyes

Rhodopsin, shown in the resting state (magenta, top view), is the photoreceptor protein of the vertebrate retina. Photoisomerization of the bound retinal chromophore (red) triggers a rigid-body helix tilt of a single helix (yellow), as dramatically demonstrated by a 6 Å increase in the distance between nitroxide spin labels attached to sites 63 and 241 (stick models). The distances were measured using DEER (Jeschke, Chemphyschem 2002, 3, 927) on an ELEXSYS E580 spectrometer.

http://www.bruker-biospin.com/brukerepr/october.html

Structural shift due to photo absorption

Page 9: photoreception : mechanisms of transduction, and non-vertebrate eyes

The photoisomerization of retinal (“primary process”, next page) is believed to be complete in only 100---200 fs, making it one of the fastest known photoreactions [Q. Wang, R.W. Shoenlein, L.A. Peteanu, R.A. Mathies, and C.V. Shank, Science 266, 422 (1994)].

Page 10: photoreception : mechanisms of transduction, and non-vertebrate eyes
Page 11: photoreception : mechanisms of transduction, and non-vertebrate eyes
Page 12: photoreception : mechanisms of transduction, and non-vertebrate eyes

In vertebrate photoreceptor cells, activated retinal begins a biochemical cascade that changes transmembrane ion permeability.

Page 13: photoreception : mechanisms of transduction, and non-vertebrate eyes

Rod and cone photoreceptors showing endomembrane system

Page 14: photoreception : mechanisms of transduction, and non-vertebrate eyes

Rh* Rh

opsin Δ conformation

opsin’s binding site for G-protein (transducin) exposed

Bound transducin’s α-Subunit can no longer hold on to GDP, so it falls off.

α-Subunit conformation now can bind GTP in place of GDP

Once GTP replaces GDP, the subunit Tα-GTP separates from the rest of transducin

The mobile Tα-GTP binds to phosphodiesterase(some may also diffuse through cytosol)

PDE*

cGMP 5’GMP

In vertebrate photoreceptor cells, activated retinal begins a biochemical cascade that changes transmembrane ion permeability.

Kee

ps io

n ch

anne

l open

Reduce cGMP pool

Page 15: photoreception : mechanisms of transduction, and non-vertebrate eyes

The proteins activated interact in the endomembrane (mostly)