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Factors Affecting Plasma Membranes
temperature
solvents
How does temperature affect plasma membranes?
phospholipids are fluid
they gain more kinetic energy
increases fluidity of the membrane and causes it to lose its structure
if temperature increases too much, the cell will break down completely
loss of structure increases the permeability of the membrane
carrier and channel proteins will be denatured at higher temperatures
Solvents
hydrophobic tails are positioned away from the water on the inside of the membrane
many organic solvents are less polar than water (e.g. alcohols) or non-polar (benzene)
these will dissolve membranes and disrupt cells
non-polar molecules can enter the cell membrane which disrupts the membrane
the membrane becomes more fluid and more permeable
can disrupt neuronal transmissions
Membrane structure
plasma membrane
formed from a phospholipid bilayer
formed from phospholipids with the hydrophilic head on the outer surface and the hydrophobic tails on the inner surface
cells are usually in aqueous environments
hydrophilic phosphate heads can interact with water
Fluid Mosaic Model
phospholipids are free to move within the layer
gives flexibility
vary in shape, size and position but fit together like a mosaic
Glycoprotein
have branching carbohydrate chains
acts as a recognition site for chemicals
play a role in cell adhesion
receptors for neurotransmitters (e.g. acetylcholine) and peptide hormones (e.g. insulin & glucagon)
Glycolipid
acts as a recognition site (e.g. in immune responses
lipids with attached carbohydrate chains
‘cell markers’
can be self or non-self
Cholesterol
stability
flexibility
lipid with hydrophilic and hydrophobic ends
regulates fluidity
prevent membranes becoming too solid by stopping the phospholipids from grouping
Extrinsic protein
partially embedded in the membrane
lying on the surface
usually have hydrophilic R-groups on their outer surfaces
Intrinsic protein (integral proteins)
spanning the phospholipid bilayer
transmembrane proteins
amino acids with hydrophobic R-groups on the external surfaces
these interact with the hydrophobic core of the membrane
Types of intrinsic proteins
Channel proteins
provide hydrophilic channel
allows passive movement of polar molecules and ions down conc gradient
held in place by hydrophobic core & R-groups
Carrier proteins
passive and active transport
involves the shape of the protein changing
Site of chemical reactions
proteins have to be in particular positions for chemical reactions to take place
examples
electron carriers and ATP synthase have to be in correct positions within the cristae
enzymes of photosynthesis are found on membrane stacks within the chloroplasts
Diffusion
The net movement of particles from a region of higher concentration to a region of lower concentration
passive process
will continue until equilibrium
random
the shorter the diffusion distance, the faster the rate of diffusion (less collision can take place)
Factors affecting the rate of diffusion
temperature
higher temp = higher rate
kinetic energy increases
concentration difference
greater conc difference = faster rate
overall movement will be larger
Diffusion across membranes
particles pass through the phospholipid bilayer
membrane must be permeable to the particles (non-polar diffuse freely)
hydrophobic core repels charged particles
polar molecules can diffuse through at a very slow rate
small molecules faster than large
membranes are partially permeable
Factors affecting diffusion rate across membranes
surface area
larger area of exchange surface = higher rate
thickness of membrane
thinner = higher rate
Facilitated diffusion
diffusion through channel proteins
protein channels are selectively permeable
can also involve carrier proteins
rate is also affected by the number of channel proteins present
Active transport
movement of molecules or ions into or out of a cell from a region of lower concentration to a region of higher concentration against the concentration gradient
requires energy and carrier proteins
act as pumps
Stages of active transport
molecule binds to receptors in the channel of the carrier protein
ATP binds to the carrier protein and is hydrolysed into ADP and phosphate
phosphate molecule binds to the carrier protein which changes shape
molecule is released into the cell
phosphate molecule released from carrier protein and combines with ADP —> ATP
carrier protein returns to original shape
Bulk transport
large molecules (e.g. enzymes)
whole cells (bacteria)
too large so move in by bulk transport
endocytosis
exocytosis
Endocytosis
bulk transport into cells
phagocytosis (solids)
pinocytosis (liquids)
cell-surface membrane invaginates when it comes into contact with material
membrane enfolds the material
membrane fuses, forming a vesicle
pinches off and moves into the cytoplasm
moves towards lysosomes
Exocytosis
bulk transport out of cells
reverse of endocytosis
vesicles (usually formed by Golgi) move towards and fuse with cell surface membrane
contents released outside of the cell
Water potential
pressure exerted by water molecules until they collide with a membrane or container
measured in Pa or kPa
pure water = 0kPa
presence of a solute lowers the water potential below 0
more conc solution = more negative Ψ
Cytolysis
animal cells
if a solution has a higher Ψ than the cytoplasm, water will move into the cell by osmosis
increases hydrostatic pressure
cell membrane can’t stretch so will burst
Hydrostatic pressure
pressure of solution in a closed system
Crenation
animal cell
if solution has a lower Ψ the cytoplasm will lose water to the solution
darker cell - conc haemoglobin
Preventing cytolysis and crenation
control mechanisms
cells continuously surrounded by aqueous solution with equal Ψ
Turgid
water enters by osmosis
Ψ higher outside the cell
hydrostatic pressure increases pressure against the cell wall (turgor pressure)
Plasmolysed
Ψ lower outside the cell
water is lost by osmosis
reduction in the volume of cytoplasm
cell-surface membrane is pulled away from the cell wall