Regulation Of Signalling Pathways Flashcards
Explain 2 ways how cells can respond to signals differently ?
1- use of different receptors
2- activating different intracellular machinery
How is the use of nicotinic or muscarinic receptors an example of how cells respond differently
Nicotinic receptors when bound to AcH cause skeletal muscle contraction
Muscarinic G protein receptors cause hyperpolarisation instead (IPSP) and
Eg reduce heart rate in heart muscle
Responses of cells needs many signalling pathways to interact. Explain 2 ways these can interact
Either molecules binding to different receptors can activate same protein to then transduce signal
Or can activate seperate proteins (phosphorylate) but then come togrther in same pathway
How is activation of PKa when adrenaline binds and cyclic amp produced = example of signals combining
PKa activates phosphorylase B but inhibits glycogen synthase at the same time (to allow production of glycogen to glucose)
What is it called when both AcH pathway and the pkA combine to activate phosphorylase kinase (glycogen into glucose) and how do they do it
Synergistic activation
PKa phosphorylates it
And ca2 released from AcH binding also activates it
How is the overlap between pathways negative? Eg by using same signal molecule
There is risk of signal producing wrong responses
Name the 3 signalling complexes that keep signals organised despite overlap
1- stabilising signalling complex
2 - transient signalling complex
3- transient by modification of phospholipids
What is the stabilising signalling complex
Use of scaffold proteins attached to receptors and all signalling proteins together = keep them together
What is transient signalling complex
Organising signal pathways by assembly of the proteins and receptor AFTER signal molecule binds
What are the sites called that help organise signalling proteins in the transient signalling complex and what do they do
Phosphoinositide docking sites
(Phosphatidyl inositol phospholipids)
They phosphorylate when receptor bound to ligand
Allows activation of proteins which bind to them
What do phosphoinositide docking sites do
Hold and activate / phosphorylate the signalling proteins (transient signalling complex)
Name the 4 ways of switching signals off (stopping things like cell proliferation)
1- removal/inactivation of signal molecule
2- removal/ inactivation of receptor
3- inactivation of signalling proteins
4- degradation of secondary messengers (eg camp)
What are the 3 ways or removing/ degrading signal molecules / explain them
1- degradation eg by enzyme (AcH esterase)
2 - recycling eg reuptake of NTs in synapse
3- SEQUESTRATION - hiding signal molecules in cleaved receptors eg in endosomes
What is receptors mediated endocytosis (how is it an example of removing a receptor to stop signal)
Receptor travels into the endosome and then into a lysosome where it is degraded (permanently)
Name the 3 ways of inactivating a signalling protein
Dephosphorylation/phosphorylation of the protein = switched off
2- GTP hydrolysis (in G proteins)
3- allosteric inactivation - dissociating the activated protein and the G protein to inactivate it