signal transduction Flashcards

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1
Q

What are the three main parts to any “classic” Signal Transduction Pathway

A

Reception: Binding of signaling molecule to a receptor
Transduction: Bring information into the cell
Response: Activates response to new information

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2
Q

What is the basic mechanism for ligand gated channels

A

We have a closed-channel protein that is turned on by a signaling molecule(ligand).
When binds, conformational changes in the protein and will open. Ions can stream into cells. Ions can enter and elicit different cellular responses

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3
Q

How do they get “turned off”?

A

When a ligand loses affinity and falls off receptor

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4
Q

What is the basic mechanism for G-Protein Coupled Receptors

A

G protein that is bound to GDP. Receptor bound to g protein. GDP=off. A signal is received a conformation change. GDP to GTP. GTP=on. Once it’s on, alpha and beta gamma subunits (they are tethered to the membrane) move until it reaches an enzyme. The alpha unit reaches an enzyme, and a second messenger is released to trigger responses

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5
Q

What is a G-protein, and what is it made of

A

trimer- alpha, beta, gamma subunits

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6
Q

How do G-Protein Coupled Receptors get turned of

A

Gtp is hydrolyzed to GDP by alpha sub unit. Signaling molecule falls off.

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7
Q

What is the basic mechanism for Receptor Tyrosine Kinases?

A

There are two receptors tyrosine kinase proteins. Signaling molecule (ligand) comes and binds to binding site.
Cause a conformational change “dimerize”. Two proteins will move together
Fully activated when 6 ATP drops off its phosphates at the protein complexes (ATP will turn to ADP)

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8
Q

How do they get turned off (transiently)

A

Can turn off when signaling molecule falls off and then have an enzyme come in to cleave off phosphates - phosphatase

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9
Q

What unique feature can turn of RTK’s permanently

A

A lysosome can recycle

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10
Q

Defects in RTK’s often show up in what disease state

A

Cancer

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11
Q

For 2nd Messengers, what are the two most common second-messenger molecules?

A

cAMP
Calcium iosn

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12
Q

How does cAMP get formed, and how is it “turned off”?
What enzyme forms cAMP, and where is it located?

A

ATP is turned to cAMP by pyrophosphate. two phosphates are cut off, to break up cAMP, phosphodiesterase breaks apart cAMP to make AMP

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13
Q

Kinase Cascades (aka Phosphorylation Cascades), what are some of the advantages of a cascade of enzymatic reactions?

A

signal amplified

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14
Q

How do some Kinase Cascades enhance the rate of signal transduction? What protein do they utilized to speed up the reaction and how does that work? b. How do Kinase Cascades turn themselves off? Is it enough to turn off the first step in the cascade?

A

signaling molecule will activate a relay molcule which can then cause to activate layes of protein kinases. Attp will phosphirilate causing a conformation change to protein kinases. Active protein kinases can turn on several more proteins that will cause cellular responses. Aplify signal all the wwyay down
To turn off, all levels have to be turned off. We need a phophotase to cleave off organic phosphate on protein kinases to turn off

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15
Q

What are some of the different general areas that we could see a cellular response

A

Metabolic pathways
Cytoskeleton movement
Transcription regulation

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16
Q

Be able to explain different examples of Coordination between different response pathways and how they can modulate any single pathway’s response.

A

Response one: Simple as a receptor binding to a signaling molecule to a receptor and creating a through relay molecules.
Two: signaling molecule binding to receptor and relay molecules branching off to make two responses.
Three: Cross-talk: where a different receptor and dif signaling molecule will cut off another signal. Activation or inhibition
Four: A different signaling molecule and receptor lead to different relay molecules that will lead to different responses.

17
Q

Yeast reproduction

A

Yeast can reproduce sexually. A and alpha cells. It will start to
A will release signaling molecule and also express receptors on its surface for the opposite mating type (alpha)
Once picked up, they mate and fuse into a hybrid , a slow response

18
Q

What benefit does this process confer on the yeast progeny

A

Its to improve genetic diversity

19
Q

What is adrenaline and where is it made?

A

Made stored and excreted in endocrine cells
Can go anywhere in the body relatively quicky and long distances
Binds to gPCR
Impact over 1700 different responses

20
Q

Which relay molecule is most commonly involved in these responses?

A

cAMP

21
Q

fast response adrenaline

A

Adrenaline binds to GPCR and activated alpha subunit of G protein. G protein activats adenylyl cyclase which can turn ATP to cAMP. cAMP turns inactive PKA to active PKA.
PKA takes ATP and releases a phosphate to inactive protein to turn on (cascade)
Glycogen degrading enzyme turned on by phospholation to break down glycogen. Liberate glucose to be used to make ATP to make energy

22
Q

slow response adrenaline

A

Slow: Adrenaline binds to GPCR and activated alpha subunit of G protein. G protein activats adenylyl cyclase which can turn ATP to cAMP. cAMP turns inactive PKA to active PKA. Active PKA is free floating and can enter nuclear pore where it can activates transcription .