Biochemistry of Vision Flashcards

1
Q

List the various layers of the Retina.

A
  1. Outer Nuclear Layer
  2. Outer Plexiform Layer
  3. Inner Nuclear Layer
  4. Inner Plexiform Layer
  5. Ganglion Cell Layer
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2
Q

Describe the general sequence of events when light hits the eye.

A

Photoreceptors –> Interneurons (Vertical and Lateral Pathways) –> Ganglion Cells

Ganglion Cells: Output cells of the retina; Axons form optic nerve; Project to the Brain; Information transmitted by Action Potentials

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3
Q

Differentiate between Rods and Cones.

A
  • *Rods:** Night Vision (differentiate between light and dark)
  • Rhodopsin (cannot detect color)
  • HIGH sensitivity and low spatial resolution
  • *Cones:** Color Detection
  • Three opsins (red, gree, and blue)
  • LOW sensitivity and HIGH spatial resolution
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4
Q

Which tissue in the human body is going to have the HIGHEST respiratory rate?

Why?

A

Rods and Cones

Dark: Na+ channels are open and the cell is depolarized (Inhibitory neurotransmitter is released when your eyes are closed!)

Light: Na+ channels are closed and the cell is hyperpolarized

**** Constantly using ATP!

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5
Q

Describe the Disc Membrane of the Outer Segment.

A
  • *GPCR System:**
    1. Rhodopsin (Receptor)
    2. Transducin (G-Protein)
    3. Phosphodiesterase (cGMP –> GMP)

Structural Protein –> Peripherin

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6
Q

Describe the strucures associated with the surface membrane.

A
  1. cGMP-gated Na+ channel (Ca2+ leak channel; tonically OPEN in the dark)
  2. Na+/Ca2+ exchanger (Ca2+ continues out after light)
  3. Guanylate Cyclase (GTP –> cGMP + PPi)
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7
Q

Describe the structure of the Photoreceptor Protein.

A

7 Transmembrane Receptor

*** Analogous to the B2-Adrenergic Receptor!

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8
Q

Describe the different states of retinal and absorption levels in regards to Schiff-Bases.

A

Resting State: Schiff-Base is Pronated

Schiff-Base linkage occurs between Lysine 296 and Retinal!

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9
Q

Describe how one can become color-blind in regards to recombination pathways among visual pigments.

Which chromosomes are the different pigments located on?

A

You can straight up LOSE one of the color-genes through recombination.

You could form a hybrid structure that is going to effect the absorption characteristics if the gene.

*** Chance of getting color blindness is GREATER for the “Red and Green” because they are on the SAME chromosome!

\*\*\*Red opsonin (500 nm) --\> Chromosome 3
Blue opsonin (420 nm) --\> Chromosome 7
Red opsonin (560 nm) --\> X
Green opsonin (530 nm) --\> X
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10
Q

Describe why the structure of the retina is a “perfect storm” for Macular Degeneration.

A
  1. High respiratory Quotient (high O2 flux)
  2. High Lipid Content
  3. UV Rays
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11
Q

What are some molecules that can protect you against macular degeneration?

A
  1. Lutein –> In Kale
  2. Zeaxanthin –> Eggs, Broccoli
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12
Q

List some good sources of food for Vitamin A.

A
  1. Carrots
  2. Dark green and leafy vegetables
  3. Sweet Potatoes
  4. Squash
  5. Broccoli
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13
Q

What are some consquences of Vitamin A deficiency?

A
  1. Night Blindness
  2. Xerophthalmia (Failure to produce tears)
  3. Keratinization of epithelium in GI, respiratory and genitourinary tract
  4. Skin becomes dry and scaly
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14
Q

Describe the production of Retinol.

A

Beta-Carotene is ingested and converted to Retinol (Vitamin A) via Dioxygenase (located in the intestinal mucosa)

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15
Q

How does Retinol travel in the blood stream?

A

Bound to Retinol Binding Protein (RBP)

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16
Q

Describe the Retinoid Cycle.

A

In the Rod Cell:

  • Light-induced change from 11-cis to all-trans
  • Release of all-trans-retinal from opsin
  • Enzymatic reduction of all-trans-retinal to all-trans-retinol
  • Exportation of all-trans-retinol (with help of iRBP)

In the Retinal Pigmented Epithelium (RPE):

  • Uptake into RPE
  • Translocation to ER
  • Esterification to all-trans-retinyl ester by lecithin retinol acyl transferase (LRAT)
  • Conversion to 11-cis-retinol by isomerohydrolase activity of RPE65
  • Enzymatic oxidation from 11-cis-retinol to 11-cis-retinal by 11-cis RDH
  • Exportation of 11-cis-retinal (with help of iRBP)

Back in the Rod Cell:

  • Uptake of 11-cis-retinal into rod cell
  • Covalent attachment (Schiff base) to opsin forming a functional rhodopsin
17
Q

Describe the different structures that are within the G-Protein Couple Receptor Complex.

A
  1. Receptor –> Rhodopsin
  2. G-Protein –> Transducin
  3. Effector Enzyme –> cGMP Phosphodiesterase
18
Q

What is the first event to happen after the photon hits the Rod Cell?

A

It hits the DOUBLE BOND and you have conversion of 11-CIS –> all-Trans

19
Q

What are the two ways to terminate the signal initated by Rhodopsin?

A
  1. Dissociation of the signal molecule from the Receptor
  2. Phosphorylation of the cytoplasmic C-terminal tail of the receptor and binding of B-Arrestin
20
Q

Describe how Ca2+ plays a role in controlling guanylate cyclase.

A

Calcium is going to inhibit the activity of the enzyme (guanylate cyclase)

In the Dark:

  • Ca2+ as well as Na+ enter the rod outer segment through the cGMP-gated channels.
  • Calcium ion influx is balanced by its efflux through an exchanger, a transport system that uses the thermodynamically favorable flow of four Na+ ions into the cell and one K+ ion out of the cell to pump one Ca2+ ion out of the cell.

In the Light:

  • After illumination, the entry of Ca2+ through the cGMP-gated channels stops, but its export through the exchanger continues
  • Thus, the cytoplasmic Ca2+ level drops from 500 nM to 50 nM after illumination.
  • This drop markedly stimulates guanylate cyclase, rapidly restoring the concentration of cGMP to reopen the cGMP-gated channels.
21
Q

Describe the concept of Amplification as it relates to absorbing light.

A