Receptor Mechanisms I and II Flashcards

1
Q

What is an antagonist

A

Something that interacts with the binding site of a natural ligand

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2
Q

How do antagonists affect the receptor

A

Prevents agonist from interacting with the receptor

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3
Q

State the 4 main types of receptors

A

Ligand gated ion channel
G protein coupled
Tyrosine kinase linked
Nuclear/steroid

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4
Q

Order the main 4 types of receptor by cellular response speed (fast - slow)

A

Ligand gated
G protein coupled
Tyrosine kinase linked
Nuclear

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5
Q

Why do nuclear receptors produce the slowest responses

A

Altering gene transcription

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6
Q

Name the four main types of ligand gated ion channels

A

Nicotinic cholinoceptor - Acetylcholine

5HT3 - 5-HT

GABAA - Gamma amino butyric acid (GABA)

Glycine - Glycine

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7
Q

Describe the structure of ligand gated ion channels

A

5 similar proteins (Pentamer)
Much diversity in subunit composition
Four transmembrane domains in each protein - 4 x 5 = 20 total in a receptor.

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8
Q

What happens when specific molecule binds to receptor

A

Molecular kink, big central pore to allow influx of ions down electrochemical gradient.

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9
Q

Describe nicotine cholinoreceptor receptor action

A

Acetylcholine released, two molecules bind to alpha subunits. Influx of sodium down electrochemical gradient. Excitatory junction potential. Takes membrane potential to a threshold where voltage gated ion channels open

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10
Q

Describe myasthesia gravis

A

Muscle nicotine AChRs become degraded and immune cells target the alpha-1 subunit. The antibodies degrade the protein and receptors disappear. A chemical is nothing without its receptor

Symptoms - Muscle weakness, fatigue, difficulty swallowing/talking

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11
Q

Describe the electrical recordings of membrane potential of a person with myaesthesia gravis against a normal person

A

At rest (normal) - small depolarisations MEPPs - miniature end plate potentials. Motor nerves releasing acetylcholine, bind to receptors for small depolarisations. Normal hyperpolarisation by acetylcholine (EJP achieved)

At rest (Myaesthesia Gravis) - Not much happens, no mepps and EJP not attained

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12
Q

How many proteins are G coupled receptors made up of

A

One, coiled up to make 3D structure

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13
Q

Compare speed and duration of ligand gated ion channels and GPCR responses

A

Ligand gated - Fast, shorter lasting
GPCR - Slow, longer lasting

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14
Q

How many transmembrane domains in GPCRs/How many times does the protein pass through the receptor

A

7

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15
Q

Describe GPCR at rest then receptor action

A

Alpha subunit binds GDP can exchange for GTP
Broken down into 4 subunits - Alpha s, i, q and 12
Protein interacts with G proteins. Receptor activated, beta and gamma interacting with enzyme, products produce cellular response. Cyclical repetition.

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16
Q

Describe GPCR action

A

Agonist binds, alpha has GTP dissociates, interacts with enzymes.

17
Q

What do each of the subunits of the alpha subunits do

A

Alpha S - turns on adenylate cyclase
Alpha I - turns down adenylate cyclase
Alpha Q - activates phospholipase C

18
Q

What enzyme does the alpha subunit contain and how is this significant

A

GTPase - Removes phosphate groups. GTP hydrolysed to GDP.

Alpha subunit then has increased affinity for beta gamma subunits than the enzyme, causing it to rebind (cyclical process)

19
Q

What does adenylate cyclase do when activated

A

Creates cAMP from ATP.
cAMP converts inactive protein kinase A to activated protein kinase A. This phosphorylates other proteins.

Level of cAMP reduced by phosphodiesterases (PDEs). They are potential targets to modify post receptor signalling.

20
Q

What does alpha GQ/11 do

A

Increases phospholipase C activity
- Works on a phospholipid in our cell membrane. Produces signal molecules - PIP2 - Phosphatidylinositol bisphosphate
Ip3 Inositol trisphosphate

21
Q

What does phospholipase C do to PIP2

A

PIP2 cleaved to Ip3 and diacylglycerol (DAG)

22
Q

What does IP3 do

A

Interacts with IP3 receptor on organelles, to release calcium

23
Q

What does DAG do

A

Activates protein kinase C