Membranes Flashcards

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1
Q

Describe uriporters, symporters, and antiporters.

A

Uniporters- moves one molecule down concentration gradient

Symporters- moves two molecules in the same direction (co-transport)

Antiporters- moves one molecule down concentration gradient and one up (co-transport)

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2
Q

Which channel allows water to flow?

A

Aquaporin

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3
Q

How does glucose require all 3 types of transporters in the small intestine?

A

Symporter- imports glucose using sodium gradient

Antiporter- sodium potassium pump to maintain sodium gradient

Uniporter- catalyses diffusion of glucose out of the cell (down its concentration gradient)

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4
Q

What does amphipathic mean?

A

Amphipathic = has both hydrophilic and hydrophobic parts

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5
Q

What are peripheral membrane proteins?

A

Membrane proteins that adhere only temporarily to the biological membrane with which they are associated. These proteins attach to integral membrane proteins, or penetrate the peripheral regions of the lipid bilayer.

They can often be ionically interacting proteins.

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6
Q

What is hydropathy?

A

Measure of energy needed to pass a segment of polypeptide into water from a solvent

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7
Q

What is an amphipathic helix?

A

A motif that shows all hydrophobic side chains on one side, so they can face into the fatty acid domain and the hydrophilic side chains on the other side.

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8
Q

What is a coiled coil domain?

A

Two alpha helices wrapped around each other to form a supercoil.

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9
Q

What is the critical micelle concentration?

A

The concentration of surfactants above which micelles form and all additional surfactants added to the system go to micelles.

> When talking about detergents

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10
Q

What is Ras and how is it located to the plasma memtbeane?

A

It is a small GTPase and is located to the plasma membrane by prenyl (a cytosolic lipid modification).

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11
Q

What is prenylation?

A

The addition of hydrophobic molecules, e.g. prenyl.

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12
Q

What is the nuclear lamina?

A

A dense fibrillar network in the nucleus of the cells. Made of lamina filaments which are prenylated.

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13
Q

What is the difference between a micelle and a liposome?

A

Micelle- monolayer of surfactant

Liposome-Bilayer of phospholipids

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14
Q

Why are hydrophobic interactions unfavourable? How is this overcome?

A

They increase the order (decrease the entropy) of water and makes it thermodynamically unfavourable.

This is overcome by hydrophobic molecules aggregating to reduce the surface area in contact with the water.

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15
Q

Why do water molecules form ice like cages around hydrophobic molecules?

A

Because there are less H bonding possibilities for each water molecule which therefore increases the bond strength for bonds that they do form

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16
Q

What do flippases do?

A

Flip phospholipids to the other side of the membrane

17
Q

What types of membranes are conical and cylindrical phospholipids associated with?

A

Conical- curved membranes

Cylindrical- flat membranes

18
Q

How would a fatty acid with 16 carbons and no double bonds be denoted?

How would a fatty acid with 16 carbons and a double bond between C8 and C9 be denoted?

A

C16:0

C16:1∆8

19
Q

What are sphingolipids?

A
  • Based on sphingosine (a long chain amino alcohol)

* Equivalent of one fatty acid and one glycerol

20
Q

What is a peroxisome?

A

Organelle containing the reducing enzyme catalase and some oxidases.

They oxidise fatty acids.

21
Q

What do proteasomes do?

A

They digest broken and unwanted proteins.

22
Q

What is phase contrast microscopy?

A

Using out of phase waves to create a higher contrast because of the constructive and destructive interference

23
Q

What is deconvolution with respect to microscopy?

A
  • Software filtering

* Working out which light has come from the near and far plane focus

24
Q

Describe SEM and TEM microscopy.

A
  • TEM-(transmission)
    • Projection image of a thin specimen
    • Specimen scatters electrons that are radiated onto it which produces an image
  • SEM-(scanning)
    • Scans the surface of an object
    • Electron gun fires thin beam of high energy electrons onto specimen
    • These high energy electrons knock out electrons in the sample
    • Electrons attracted towards detector