Ion Channels+some Hemostasis bcs why not Flashcards

1
Q

How many K ions are in the K channel at any given time, and in what position

A

2.

1-3 position/2-4 position (separated by water molecules)

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2
Q

What is the role of kir6.2 and SUR1?

A

(ATP sensitive K channel subunits in pancreatic b cells)

ATP/ADP ratio increases -> ATP sensitive K channel shut down -> depol. -> insulin secretion

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3
Q

Where does kir6.2+SUR localized in the body?

A

Pancreatic B cells

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4
Q

Which technique reveals opening and closure of individual ion ch pores?

A

Patch clamp technique

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5
Q

Define- open propability

A

Total time spent in open state divided by the total observation time

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6
Q

Mutation in the kir6.2 SUR1 and symptoms (and treatment)

A

Persistent hyperinsulinemia hypoglycemia (PHHI)
As the name implies
We can treat with Diazoxide (helps open the channel)

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7
Q

How does the Cl- channel pore stabilizes?

A

Helix dipole

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8
Q

Requirements for activation of CFTR Cl- channel

A

Phosphorylation by cAMP dependent PKA (at least 10 serine residues in the regulatory domain)

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9
Q

Drug that inhibits platelets activation?

A

Aspirin

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10
Q

Mutation in Cl- channel will cause

A

Myotonia.
Unstable resting potential
Hyperactive muscle fiber

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11
Q

What is the pro-coagulant effect of thrombin-TM complex?

A

Inhibits fibrinolysis by cleaving TAFI into its active form

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12
Q

Where can we find Cl- channel 1 (Clc1)

A

Skeletal m

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13
Q

Describe the gating mechanism of ATP sensitive K channel (activation by…. inhibition by….)

A
ATP inhibits (also Sulfonylurea)
ADP activates (also Diazoxide)
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14
Q

Why does the Na ion excluded from the K channel?

A

Na is smaller than K -> Na coordination is energetically unfavorable

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15
Q

ATP sensitive K channel SUR structure

A

3 TMD

2 intracellular NBD (Nucleotide Binding protein)

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16
Q

How is the ATP sensitive K channel blocked while Depol.

A

By Mg ions from intracellular side

17
Q

How each K ion is stabilized in the K channel

A

Coordinated with 8 carbonyl oxygens (mimicking hydration shell)

18
Q

Triggers for platelet activation?

A
Thrombin
Collagen
PAF
Thrombaxane
ADP
19
Q

How does the CFTR pore closes?

A

NBD2 hydrolyses ATP -> dimer dissosiates

20
Q

What does the phosphorylated CFTR Cl channels need for gating?

21
Q

ATP sensitive K channel structure

A

Octamer built from
4 times Kir6.2
4 times SUR (Sulfonylurea Receptor)

22
Q

What is the throughput of K channel

A

1-2X10^8 ions/s

23
Q

Describe the structure of the K+ channel

A

Tetramer (each subunit contains 6TM helicels

P-loop btw. S5 and S6 (selectivity filter)

24
Q

What does COX enzyme produces?

A
  1. Prostaglandins- pro inflammatory

2. Thrombaxane- promote clotting (aggregation of platelets)

25
What is the role of kringle domain in the structure of tPA and plasminogen?
Lys binding
26
What are the substrates of fVIIa?
fX And fIX
27
CFTR structure
``` (ABC protein family) Single polypeptide chain -2 TMD -2 intracellular NBD -Regulatory domain ```
28
On what subunits subunit of ATP sensitive K channel does ATP acts on?
Kir6.2
29
Structure of the Cl- channel (Clc)
Homodimer, both subunits individually form separated pores (two total)
30
Who works on the SUR subunit? (ATP sensitive K channel)
ADP Sulonylurea k channel openers
31
Define throughput rate
Number of ions transported through a channel in a given time
32
Mutation in CFTR Cl- channel will cause
Cystic fibrosis (mucoviscidosis)
33
What is the role of Cl- channel 1 (Clc1) in its tissue?
Tissue-skeletal m | Job- stabilizes resting memb potential
34
What acts as voltage sensors on the voltage gated K ch?
Lys and Arg residues
35
What is the active conf. Of CFTR?
NBD1-NBD2 heterodimer , 2xATP btw. them -> open pore
36
Where does the ATP binds the CFTR?
2x ATP bounds the (2) NBD