Module 9 Flashcards

1
Q

Membrane functions

A

Seperate cells from the external medium to create an intracellular environment of unique and defined composition
Allows selective transport of substrates in and out of the cell

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2
Q

Lipid Bilayer

A

Basic Structural element of membranes
Membrane formation is a consequence of the amphipathic nature of the membrane lipids
These molecules self assemble through the hydrophobic effect

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3
Q

Fatty Acids Favour

A

Micelle formation

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4
Q

Lipid Bilayers

A

Form membrane Vesicles
Exposure of hydrophobic tails at the edge of the bilayer to water is energetically unfavourable
Flat bilayer sheets are unstable and spontaneously form membrane vesicles with an internal volume
These Vesicles are the basis of cells and organelles

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5
Q

Impermeable membrans

A

Lipid bilayer membranes have a vert low permeability to ions and Most polar molecules
Permeability of small molecules is correlated with their relative solubility in water
Some small non polar gases like O2 and CO2 can pass directly through the membrane

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6
Q

Vesicles for Drug delivery

A

The cell membrane can represent a critical barrier per polar drug intended for intracellular targets
Encapsulation of a drug within a liposome can facilitate transport across the membrane
Liposomes can also be used to target specific cells and organ;lleles

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7
Q

Membranes have

A

Higher ratio of protein than lipids

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8
Q

Fluid Mosaic Model of Membrane structure

A

Membranes are dynamic structures due to the nature of the non covalent interactions
lipids and proteins freely diffuse in the plane of the membrane
Lateral movement of proteins and lipids within the membrane is very rapid
Movement across the membrane is restricted

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9
Q

Transbilayer movement requires Catalysis

A

Transbilayer movement requires a polar head group to pass through hydrophobic environment
Uncatalyzed rate of lipid molecule crossing from one sheet to the other (Flip flop) is very slow

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10
Q

Flippases

A

Translocation of lipids form one side of bilayer to other is catalyzed by enzymes called flippases

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11
Q

membrane fluidity

A

Cells need to maintain an appropriate levels of membrane fluidity
Membranes undergo temperature - dependant phase transitions
Cells can adjust membrane composition to maintain liquid - ordered state

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12
Q

Below the phase transition temp

A

Membrane is too solid

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13
Q

Above the phase transition temp

A

Membrane is too fluid

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14
Q

At the phase transition temp

A

just right

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15
Q

Lipid Rafts

A

Arise from the spontaneous association of lipid molecules whose hydrocarbon tails are of similar length
Sphingolipids (With longer tails) for clusters that excel glycerphospholipids
Longer saturated hydrocarbons of sphingolipids form stable association making the rafts thicker and more orders than the rest of the membrane
Rafts are docking points in lipid anchored proteins that contain long chain saturated fatty acid anchors
Lipid linked proteins that associate with rafts often serve signalling functions

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16
Q

Types of Membrane Proteins

A

Peripheral
Lipid Anchored
Intergral membrane proteins

17
Q

Peripheral Membrane Proteins

A

Associate with membrane through electrostatic or hydrogen bonding interactions
Can dock to either membrane lipids or integral membrane proteins
The bulk of the peripheral membrane proteins is in the cytosol or extracellular space
Changes in pH or ionic strength often releases these proteins from the membrane

18
Q

Lipid Anchored Proteins

A

Covalently attached lipids can anchor proteins to the membrane
These protein modifications are sometimes reversible, allowing for regulation of cellular location
GPI anchored protein are always at the outer face
Proteins with single chain hydrocarbons always to inner face

19
Q

Integral Membrane Proteins

A

Integral membrane proteins are immersed in and usually span the membrane
Protein positioning within a membrane is specific and directional
Integral membrane proteins tend to be of 3 varities

20
Q

3 types of integral membrane proteins

A

a- helical, a-helical bundles and B- barrels

21
Q

Hydrogen Bonding within membrane spanning regions

A

Side chains within the transmembrane region tend to be non polar however the carbonyl and amide groups of each peptide bond are polar
Polar unpaired carbonyl and amide groups in the bilayer core are energetically unfavourable
Carbonyl and amide group of the protein backbone within the bilayer have to be hydrogen bonded

22
Q

Simple Diffusion

A

Non polar gases (O2 and CO2) and hydrophobic molecules can directly cross the membrane
Their direction and rate of movement determined by their concentrations on either side of the membrane
Diffusion can only result in the net movement down a concentration gradient

23
Q

Facilitated Diffusion

A

Membrane transporters lower the activation energy barrier of crossing the bilayer
Activation energy for removing the hydration shell from a polar solute and transferring it into the non polar environment in the core of the bilayer is very high
Membrane transporters lower the activation energy for crossing the membrane by replacing the hydration shell with interactions with polar groups along the transfer path in the protein interior

24
Q

Channel Proteins

A

Membrane pore to transport molecules down conc gradient
hIgh conductance rates because they bind the substrate very weakly
Do not Saturate

25
Q

Carrier Proteins

A

Membrane proteins that undergo substrate induced conformational change, or membrane repositioning to release substrate to the other side of the membrane
Slower bevause they bind to substrate quite strongly
Can saturate

26
Q

Glucose Permease of Erythrocytes

A

Facilitated Diffusion through carrier
Specific to D- Glucose
Rate of uptake follows a pattern of resembling M-M kinetics
Kt about 1/3 concentration of blood glucose so the transporter is nearly saturated and operates near Vmax

27
Q

Coupled Transport

A

Transport of a single molecule is called uniport
Some transporters couple the movement of two molecules

28
Q

Antiport

A

Move molecules is different directions

29
Q

Symport

A

Move molecules in same directions

30
Q

Primary Active Transport: P Type ATPase

A

Cells maintain high gradients of Na+ outside the cell and K+ inside the cell
The gradient controls cell volume, electrical excitability, and enables uptake of nutrients through secondary active transport system
Maintaining activity the Na K sumo requires about a third of your energy
Na K ATPase pumps 3 Na+ out of the cell and two K+ Into the cell
Called P type as it undergoes a phosphorylated intermediate

31
Q

V type ATPases

A

Use the energy of ATP to move protons against a concentration gradient
Acidification of organelle
In chloroplasts and mitochondria, F type ATP synthases reverse this reaction to use proton gradients to generate ATP

32
Q

ABC Transporters

A

Contain ATP binding domains
Transport of a variety of biomolecules out of the cell against a concentration gradient
Multi drug resistance protein pumps drugs out of the cell rendering the drug ineffective

33
Q

Seconded Active Transport (Glucose Uptake into Intestinal Epithelial cells)

A

In intestinal epithelial cells glucose uptake from the gut in driven through symport with Na_+
The movement of glucose up its concentration gradient is enabled by the movement of Na+ions down their concentration

34
Q

Ion channels

A

Ion channels enable rapid movement of ions across the membrane\Actions of ion channels can cause changes in membrane potential

35
Q

K+Channel

A

k+ channels allow rapid movement of K+ ions out of cell
Although Na is small the channel os 100 fold more permeable to K