PLASMA MEMBRANE
STRUCTURE
Phospholipid bilayer
Protein molecules embedded
partially or entirely
Scattered throughout
proteins span the membrane
with hydrophilic (water loving)portions facing out and hydrophobic (water hating) portions facing in
Fluid consistency (like olive
oil)
Called the ‘fluid-mosiac
model’
http://www.youtube.com/wa
ASYMMETRY AND
ARRANGEMENT:
The upper and lower portions of the membrane are not
the same (identical)
Same basic components, but arrangement may vary
between the two halves
Carbohydrate chains of the glycolipids and glycoproteins
MEMBRANE FLUIDITY
Molecules can be
‘exchanged’
horizontally, giving the membrane its fluid quality.
Molecules cannot be
‘exchanged’ or move on a vertical plane. This maintains the integrity of the
THE LIPIDS
Phospholipids arrange themselves into a
bilayer with their hydrophobic tails facing each other, and the hydrophilic heads facing both the intracellular and extracellular fluids of the cell.
Glycolipids have a head which is a chain of
sugars forming a carbohydrate. (similar in structure otherwise to phospholipids)
Cholesterol – found in animal cells and helps
CELL FINGERPRINTS
Carbohydrate chains serve as ‘fingerprints’
for the cell
Sequence and diversity of chains vary from
species to species making each cell unique
Make cell recognition possible within the
body
Foreign cells are destroyed by the immune
system
Cells of different blood type, or foreign
TYPES OF PROTEINS
1. Channel protein
2. Carrier protein
3. Cell recognition protein
4. Receptor protein
CELL RECOGNITION PROTEIN
Allows the body to recognize its own cells,
and foreign cells
Makes transplants difficult, as well as blood
RECEPTOR PROTEIN
Shaped so that certain molecules bind to
CHANNEL PROTEIN
Allows particular molecules or ions to cross
CARRIER PROTEINS
Combine with an ion or molecule before
transporting it
Makes the membrane ‘differentially or
selectively permeable’ because it only allows certain molecules and ions to pass
Are specific; only combine with specific
molecules
Combines with molecule, changes shape and
TRANSPORT ACROSS A
MEMBRANE
http://
www.wiley.com/college/pratt/0471393878/s tudent/animations/membrane_transport/ind ex.html
• Typically, a cell must transport various
materials back and forth across its membrane.
• These materials include water, waste,
FACILITATED TRANSPORT USING
CARRIER PROTEINS:
Large molecules such as glucose and amino acids down a concentration
gradient.
Eg. glucose carrier protein changes shape ‘back and forth’ approximately
100 times per second.
Glucose binds to protein, protein closes behind molecule and passes it
through to the cytoplasm
After glucose is released, carrier protein changes back to original shape
FACILITATED TRANSPORT
This facilitated transport by the carrier
ACTIVE TRANSPORT
Also uses a carrier protein (called a ‘pump’),
but this time, cellular energy as well
Ions or molecules move across the membrane
and accumulate either inside or outside the cell
These molecules often move in the opposite
direction of the concentration gradient
Eg. sodium ions in urine cells, iodine in the
thyroid gland or the sodium-potassium pump
40% of the cell’s energy is used in this
SODIUM POTASSIUM PUMP
Carrier protein changes shape asthe sodium and potassium bind, allowing it to combine
alternately with each ion
Change in shape is facilitated by
a phosphate group which is donated by ATP
Watch this animation:
ACTIVE VS. FACILITATED
1) Compare/contrast active vs. facilitated
DIFFUSION AND OSMOSIS
Diffusion – movement of molecules from high
to low concentration
‘Down the concentration gradient’ until
concentrations are equal on both sides of the cell membrane
Osmosis is the diffusion of water across the
cell membrane (following the same principal)
Eg. dye in water (solute – dye, solvent –
water)
VESICLE FORMATION AND THE TRANSPORT
OF MATERIALS WITHIN THE CELL:
Cells will manufacture molecules for secretion outside of the cell.
Some of these secretion molecules are complex combinations of proteins,
carbohydrates and lipids.
Watch this animation:
http://
www.sumanasinc.com/webcontent/animations/content/vesiclebudding.html
1. Protein is synthesised and present in the rER.
2. The protein is moved through the rER and modified.
3. A spherical vesicle is formed form the end of the rER with the protein inside. 4. The vesicle migrates to the golgi apparatus.
5. Vesicle and golgi membranes fuse. The protein is released into the lumen of
the golgi apparatus.
6. The golgi modifies the protein further by adding lipid or polysaccharides to
the protein.
7. A new vesicle is formed from golgi membrane which then breaks away. The
vesicles migrates to the plasma membrane.
8. The vesicle migrates to the plasma membrane fuses and secretes content its
ENDOCYTOSIS AND EXOCYTOSIS
The fluidity of the membrane allows it to change
shape, break and reform during endocytosis and exocytosis.
Watch this animation:
http://highered.mcgraw-hill.com/olcweb/cgi/