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?

A

ATP

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
Q

What is the role of kringle domain in the structure of tPA and plasminogen?

A

Lys binding

26
Q

What are the substrates of fVIIa?

A

fX
And
fIX

27
Q

CFTR structure

A
(ABC protein family)
Single polypeptide chain
-2 TMD 
-2 intracellular NBD
-Regulatory domain
28
Q

On what subunits subunit of ATP sensitive K channel does ATP acts on?

A

Kir6.2

29
Q

Structure of the Cl- channel (Clc)

A

Homodimer, both subunits individually form separated pores (two total)

30
Q

Who works on the SUR subunit? (ATP sensitive K channel)

A

ADP
Sulonylurea
k channel openers

31
Q

Define throughput rate

A

Number of ions transported through a channel in a given time

32
Q

Mutation in CFTR Cl- channel will cause

A

Cystic fibrosis (mucoviscidosis)

33
Q

What is the role of Cl- channel 1 (Clc1) in its tissue?

A

Tissue-skeletal m

Job- stabilizes resting memb potential

34
Q

What acts as voltage sensors on the voltage gated K ch?

A

Lys and Arg residues

35
Q

What is the active conf. Of CFTR?

A

NBD1-NBD2 heterodimer , 2xATP btw. them -> open pore

36
Q

Where does the ATP binds the CFTR?

A

2x ATP bounds the (2) NBD