Receptors Ch 5 & 8 Flashcards

1
Q

Structure of receptors

A

Globular proteins, mostly in the cell membrane. Contains a hydrophobic hollow or cleft on its surface that functions as binding site.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Function of receptors

A

Receive messages from chemical messengers and transmit them into the cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

2 Types of Chemical Messengers
Released from?
Lifespan?

A

Neurotransmitters: released from nerve endings that cross a synapse to bind to receptor. Short lived. Between individual cells.
Hormones: released from gland and bind to target cells throughout the body.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Chemical Messenger definition and 6 specific ex.

A

Switch on receptors without undergoing a chemical reaction. Ex. acetylcholine, adrenaline, dopamine, serotonin, aminobutyric acid, glutamic acid.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Signal Transduction

A

Domino effect resulting from induced fit when messenger binds via weak forces leading to chemical signal inside cell.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Binding interaction strength

A

Strong enough to hold messenger for signal transduction to take place.
Weak enough to allow messenger to depart.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Antagonist

A

Bind more strongly than messenger to binding site, but does not elicit response

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Agonist

A

Binds reversibly to binding site and elicits response. Similar in structure to natural messenger.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Ion channel structure

A

Five glycoprotein subunits tranversing cell membrane with receptor integrated into alpha helix subunits making hydrophillic channel in center. Has open and closed conformation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Ion channel function

A

Allow specific ions to to cross cell membrane down concentration gradient, depolarizes nerve membranes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Inhibitory vs. Excitatory ion channels with examples

A

Inhibitory: Chloride ions (ex. GABA)
Exhibitory: Potassium, Sodium, Calcium ions (ex. nicotinic)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

G-protein coupled receptor with example

A

7 pass transmembrane helix with ligand binding site on the extracellular side and G-protien binding site on intracellular side (ex.Rhodopsin)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

G-protein coupled receptor function

A

Binding of messenger leads to induce fit that causes G protein to bind and bind GTP (enzyme function), splitting into alpha and beta-gamma subunits.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

G-protein function with 2 examples

A

Alpha s subunit activates membrane bound enzyme (ex. adenylate cyclase, phospholipase C). Inactivated when GTP is hydrolyzed to GDP.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Adenylate cyclase

A

Activated by alpha s subunit, converts ATP to cyclic AMP.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Competitive reversible antagonist

Effect of increasing concentration of messenger?

A

Binds noncovalently but different induced fit occurs so receptor is not activated. Increasing concentration reverses antagonism.

17
Q

Non competitive irreversible antagonists

Effect of increasing concentration of messenger?

A

Binds covalently but different inducted fit occurs so receptor is not activated. Increasing concentration has no effect.

18
Q

Noncompetitive reversible allosteric antagonist

Effect of increasing concentration of messenger?

A

Binds noncovalently to allosteric site. Increasing concentration has no effect.

19
Q

Antagonists by proximity effect

A

Binds reversibly to neighboring binding site and overlaps with messenger binding site (Noncompetitive).

20
Q

Partial agonist

A

Binds to receptor but causes conformational change that is not ideal or is able to bind to receptor in two ways, acting as an agonist in one method and as an antagonistic in the other.

21
Q

Inverse agonist

A

Binds to receptor and shuts down constitutive activity.

22
Q

Super agonist

A

Binds to receptor and elicits more than full biological response.

23
Q

Desensitization/Sensitization

A

Desensitization: endocytosis of receptors or reduced receptor biosynthesis, phosphorylation of receptor.
Sensitization: increased receptor synthesis.

24
Q

Dependence

A

need to take drug to have normal response that can occur with both agonists and antagonists due to increase receptor synthesis (sensitization).

25
Q

Alpha s subunit

A

Stimulates adenylate cyclase

26
Q

Alpha i subunit

A

Inhibits adenylate cyclase and may activate potassium channel

27
Q

Alpha o subunit

A

Inhibit neuronal calcium ion channels

28
Q

Alpha q subunit

A

Activates phospholipase C

29
Q

Tolerance

A

Higher dosage of drug required to produce the same effect by increasing the number of receptors.

30
Q

Phospholipase C

A

Cleaves phosphatidylinositol diphosphate (PIP2) into diacylglycerol (DG) and inositol triphosphate (IP3).

31
Q

Diacylglycerol

A

Hydrophobic secondary messenger activate protein kinase C (PKC).

32
Q

Inositol triphosphate

A

Hydrophilic secondary messenger that opens calcium channels in the endoplasmic reticulum to activate calcium dependent protein kinases and calmodulin.