M&R Receptor effector mechanisms Flashcards
What are the 3 types of cell surface receptor?
- Ligand-gated ion channels e.g. nAChR
- Receptors with intrinsic enzymatic activity (protein kinases) e.g. insulin receptor. Enzyme phosphorylates the enzyme itself & other substrates
- G protein coupled receptors e.g. mAChR
How do GPCRs respond to stimuli and cause a change in cellular activity?
An activated GPCR reacts with a G-protein (3 subunits - a, B, gamma)
The GPCR- G protein interaction activates the G protein by causing GTP to exchange for GDP on the alpha subunit (GTPase)
The alpha + beta,gamma complex dissociates into alpha GTP and free beta gamma subunits
Each subunit can then interact with effector proteins e.g. second message-generating enzymes or ion channels
What is the general structure of a GPCR?
Single polypeptide chain
7 transmembrane domains
Extracellular N terminal
Intracellular C terminal
How is a G-protein signal terminated?
The alpha-GTP and beta-gamma interactions with effectors last until the alpha subunit GTPase hydrolyses GTP back to GDP.
Alpha-GPD and better-gamma subunits then reform
Give some broad examples of effectors
- enzymes e.g. adenylyl cyclase ATP –> cAMP, phospholipase C
- ion channels e.g. voltage operated Ca2+ channels
How is adenylyl cyclase regulated?
Adenylyl cyclase can be regulated by agonist-stimulation such as
- B-adrenoreceptors
- a2-adrenoreceptors
How does adenylyl cyclase exert its actions?
Through cAMP dependent protein kinase (PKA)
cAMP binds to the regulatory subunits of PKA which activates the catalytic subunits
The catalytic subunits then phosphorylate target proteins in the cell
Describe the role of phospholipase C
Phospholipase C catalyses the cleavage of membrane phospholipid PIP2 into two secondary messengers: IP3 and DAG.
(PIP2 – phospholipase C —> IP3 + DAG)
IP3 binds to the IP3 receptor on the ER
This releases CA2+
Calcium then binds to phosphokinase C, which binds to DAG
How is phospholipase C regulated?
Phospholipase C can be regulated by agonist stimulation
eg
- a1-adrenoreceptors
- M1 muscarinic receptors
Give examples of signalling pathways in the body
- Inotropy in the heart
Adrenaline and NA interact with B1-adrenoreceptors to increase force of contraction by increasing the opening of VOCCs. - Smooth muscle contraction
NA interacts with a1-adrenoreceptors to cause vasoconstriction (IP3 releases Ca2+)
ACh can interact with bronchiole M3-muscarinic receptors to cause bronchoconstriction
(all utilise the GCPR - phosoplipase C - IP3 / DAG - phosphokinase C pathway)
- Neurotransmitter release
In CNS and PNS neurotransmitter release is modulated by presynaptic GPCRs. The beta-gamma subunit inhibits voltage operated Ca2+ channels reducing Ca2+ influx.