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Cell Membranes
Fluid Mosaic Model
Selectively permeable
Made of two layers of phospholipids, with the following embedded components - integral proteins, peripheral proteins, glycoproteins, glycolipids, carbohydrates, cholesterol
Bordered on one side by extracellular matrix, and on the other side by the cytoskeleton
Aquaporins - membrane proteins that transport water only
One aquaporin enables billions of water molecules to pass through the membrane per second!
Phospholipids
hydrophilic phosphate heads and hydrophobic fatty acid tails
Amphipathic
having both hydrophilic and hydrophobic parts.
Phospholipids are amphipathic.
Most membrane proteins are also amphipathic.
Lateral Movement
Lateral movement is what provides the membrane with a fluid structure
Most of the lipids and some of the proteins can shift about laterally.
Lateral movement of phospholipids within the membrane is rapid.
Proteins are much larger than lipids and move more slowly, but some membrane proteins do drift.
Some membrane proteins seem to move in a highly directed manner, maybe driven along cytoskeletal fibers by motor proteins.
Many other membrane proteins seem to be held immobile by their attachment to the cytoskeleton or to the extracellular matrix.
Membrane Fluidity
Membrane remains fluid as temperatures decrease, until phospholipids pack into a closely-packed arrangement and the membrane solidifies.
The temperature at which the membrane solidifies depends on the types of lipids it is made of.
If the membrane is rich in phospholipids with unsaturated fatty acid tails, remains fluid to a lower temperature (due to kinks).
Cholesterol
Has different effects on membrane fluidity at different temperatures
Makes membranes less fluid by restraining phospholipid movement
Also hinders close packing of phospholipids, so it lowers the temperature required for membrane to solidify
Helps membrane resist changes in fluidity, when the temperature changes
When temperatures increase, prevents membrane from flowing too fast. (speed bump)
When temperatures decrease, prevents membrane from solidifying. (wedge)
Membrane Fluidity
Membranes must be fluid to work (salad oil!)
When a membrane solidifies, permeability changes, and enzymatic proteins in the membrane may become inactive.
Membranes that are too fluid cannot support protein function, either.
Extreme environments pose a challenge.
Evolutionary adaptations that include differences in membrane lipid composition:
Some organisms can change the proportion of unsaturated phospholipids in their membranes in response to winter cold or extreme heat.
Natural selection has favored organisms whose mix of membrane lipids has ensured an appropriate level of membrane fluidity for their environment.
Membrane Proteins - Integral proteins
Most membrane functions are carried out by proteins.
Penetrate the hydrophobic interior of the lipid bilayer
Majority are transmembrane proteins, which span the membrane
Others extend only partway into the hydrophobic interior
Hydrophobic regions of an integral protein consist of one or more stretches of nonpolar amino acids, usually coiled into alpha helices
Hydrophilic parts of the molecule are exposed to the aqueous solutions on either side of the membrane
Some proteins also have one or more hydrophilic channels that allow passage of hydrophilic substances.
Membrane Proteins - Peripheral proteins
Most membrane functions are carried out by proteins.
Not embedded in the lipid bilayer at all
Loosely bound to the surface of the membrane, often to exposed parts of integral proteins
On the cytoplasmic side of the membrane, some membrane proteins are held in place by attachment to the cytoskeleton
On the extracellular side, some membrane proteins are attached to fibers of the extracellular matrix
Functions of Membrane Proteins, 1-3
Transport - may provide a hydrophilic channel (channel proteins) across the membrane that is selective for a particular solute - may shuttle a substance from one side to the other by changing shape (ATP) (carrier proteins)
Enzymatic activity
Signal transduction - membrane protein (receptor) may have a binding site with a specific shape that fits the shape of a chemical messenger, such as a hormone - the external messenger (signaling molecule) may cause the protein to change shape, allowing it to relay the message to the inside of the cell, usually by binding to cytoplasmic protein
Functions of Membrane Proteins, 4-6
4. Cell-to-Cell Recognition - some glycoproteins serve as ID tags that are specifically recognized by membrane proteins of other cells (may be short-lived)
5. Intercellular joining - membrane proteins of adjacent cells may hook together in various kinds of junctions, such as gap junctions or tight junctions (long-lasting)
6. Attachment to cytoskeleton and extracellular matrix (ECM)- microfilaments or other elements of the cytoskeleton may be noncovalently bound to membrane proteins - helps maintain cell shape - stabilizes location of certain membrane proteins
Role of Membrane Carbs in Cell-Cell Recognition
Membrane carbs are usually short, branched chains of fewer than 15 sugar units
Some are covalently bonded to lipids - glycolipids
Most are covalently bonded to proteins - glycoproteins
Carbs on the extracellular side of the membrane vary from species to species, among individuals of the same species, even from one cell type to another in an individual
Diversity of the molecules and their locations on the cell’s surface enable membrane carbs to function as markers that distinguish one cell from another
A, B, AB, O blood types - arise from variation in the carb part of glycoproteins on surface of red blood cells
Synthesis and Sidedness of Membranes
Membrane proteins and lipids are made in the ER.
In ER, carbs are added to transmembrane proteins, making them glycoproteins.
Inside Golgi bodies, glycoproteins undergo further carb modification, and lipids acquire carbs, becoming glycolipids.
Glycoproteins, glycolipids, secretory proteins are transported in vesicles to membrane
Vesicles fuse with membrane
Outside face of vesicle becomes continuous with cytoplasmic face of membrane
Releases secretory proteins from cell (exocytosis)
Positions the carbs of glycoproteins and glycolipids on outside face of membrane
Membrane Structure Results in Selective Permeability
Nonpolar molecules like hydrocarbons, CO2, O2 are hydrophobic.
They can dissolve in the lipid bilayer and cross it easily, without aid of membrane proteins.
Ions and polar molecules cannot pass through hydrophobic interior of membrane.
Hydrophilic molecules cross through transport proteins - ex. channel proteins, aquaporins, carrier proteins (glucose transporter is so specific it rejects fructose!)
Movement of Molecules Across Membranes
Diffusion
Osmosis
Passive transport (facilitated diffusion)
Active transport
Diffusion
Molecules move HIGH to LOW
Down a concentration gradient
Lots of molecules → fewer molecules
Can occur in air, liquid, or across membranes
Ex. Oxygen, Carbon Dioxide
Molecules travel through phospholipids, down a concentration gradient, from high concentration to low concentration.
Osmosis
Diffusion of WATER only
Aquaporins
Only occurs through membranes
High water to low water
Hypertonic solutions - solutions that have a higher solute concentration than the cells found in that solution - water always LEAVES the cells (plasmolysis)
Hypotonic solutions - solutions that have a lower solute concentration than the cells found in that solution - water always ENTERS the cells
Isotonic solutions - solutions that have an EQUAL solute concentration with the cells found in that solution - NO NET MOVEMENT of water
Passive Transport (Facilitated Diffusion)
Large or charged molecules
Through a protein (channel or carrier)
High to Low - down a concentration gradient
NO ATP required
Ex. sugar, salt, ions
Channel proteins that transport ions are called ion channels.
Many ion channels are gated channels, which open or close in response to a stimulus.
Active Transport
Large or charged molecules
Through a protein ( ALL carriers)
Low to High - AGAINST the concentration gradient
ATP required
Ex. sugar, salt, ions