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what is the most abundant lipid
phospholipids
what does amphipathic mean
hydrophobic and hydrophillic
what are the two classes of phospholipids
phosphoglycerides and sphingolipids
phosphoglyceride structure
phosphate group links to polar head group
sphingolipid structure
sphingosine as the backbone rather than glycerol, one fatty acid chain and amide bond
types of sphingolipids
ceramides, sphingomyelin, glycosphingolipids
ceramides
form the base structure for the other two types of sphingolipids, one fatty acid chain is attached to sphingosine with amide bond
sphinomyelin
ceramide bound with phosphocholine or phosphoethanolamine
glycosphingolipids
ceramides with one or more sugar residues
what are the two types of glycosphingolipids
cerebrosides, gangliosides
what does it mean for the membrane to be fluid
phospholipids drift laterally or rotate
what are factors that affect fluidity
high temperatures, short fatty acid chains, unsaturated fatty acids
why are shorter fatty acid chains better than long
less surface area to allow for stabilizing van der waals or hydrophobic interactions
why are unsaturated fatty acids better than saturated
kinks/bends due to C=C prevent packing
how does cholesterol affect fluidity
warm temperatures restrain movement of phospholipids, cool temperatures prevent tight packing
how does cholesterol affect membrane permeability?
increase in cholsterol decreases permeability
what are lipid rafts composed of
enriched in cholesterol, sphingomyelin, gangliosides and phosphoglycerides with saturated fatty acid chains
how does the composition of lipid rafts affect the membrane
the components are packed tightly to reduce fluidity and the composition causes thickening of the bilayer to recruit proteins with long transmembrane domains
what are the functions of lipid rafts
organizing centers for the assembly of signalling molecules, recruiting actin cytoskeleton, facilitating the formation of transport vesicles
what are the functions of membrane proteins
transport, enzymatic activity, signal transduction, cell-to-cell recognition, intercellular joining, attachment to cytoskeleton and extracellular matix
where are carbohydrates located
outer leaflet for cell to cell recognition
what are carbohydrates (glucose and galactose) bound to
lipids or proteins
what is a subgroup of glycolipids
glycosphingolipids
what are the three reasons as to why asymmetry is important
surface potential difference
creates curvature in membrane
preservation of cell viability
how does surface potential difference work
outer leaflet- PC, sphingomyelin, glycolipids
inner leaflet- PS, PE, PI
PS and PI have net negative charges and interact with positive charged amino acid residues so the proteins remain anchoredI
PC, PS, PE, PI (what do they stand for)
phosphatidylcholine, phosphatidylcerine, phosphatidylethanolamine, phosphatidylinositol
how does curvature in the membrane work
insertion of cone-shaped phospholipids (PE) promote curvature
cylindrical shape (PC, PS, PI, sphingolipids) create the bilayer
how does the preservation of cell viability work
the extracellular expression of PS targets the cell for engulfment by macrophages (cell apoptosis)
what does selective permeability mean and how is it regulated
not everything can pass through, regulated by the hydrophobic interior and hydrophilic exterior
how is the concentration and electrical gradient established
movement of ions in and out
what is the charge of the interior of the cell
negative
how do the Na+ gradients work in living cells
concentration gradient and electrical gradient drive Na+ into the cell
how do the K+ gradients work
electrical gradient drives it into the cell, concentration gradient drives it out
electrochemical gradients
combined gradients
what direction does the concentration gradient move if you are going from high to low
down
passive transport
no energy is needed from the cell
examples of passive transport
simple and facilitated diffusion
how does facilitated diffusion work
transport proteins move molecules
what are the 3 main proteins of facilitated diffusion
porins, permease, carriers, ion channels
porins
large, non selective, barrel shaped transport proteins that move molecules based on size
permease carriers
facilitate transport of specific molecules across membrane by having molecules bind to induce a conformational change
when do permease carriers become saturated
when all binding sites are occupied
ion channels
form small pores that only specific ions can pass through based on size and charge
what are the five types of ion channels
ligand-gated (regulatory molecules)
voltage gated (membrane potentials)
mechanogated (subcellular proteins in cytoskeleton)
signal-gated (intracellular molecules)
leak channel (not gated, intrinsic rate of switching)
active transport
requires energy (ATP) to move substances, substances diffuse against concentration gradient
what are the types of active transport
primary and secondary active transport
primary active transport
involves permease carrier proteins and uses an exergonic reaction to provide energy to transport a molecule
example of primary active transport
Na+ - K+ pump moves Na+ using atp to establish a sodium concentration gradient
secondary active transport
permease carrier proteins that move one molecule down its electrochemical gradient to help another move against its concentration gradient
what is a key difference between primary and secondary active transport
primary uses atp, secondary uses electrochemical energy
example of secondary active transport
sodium moves along Na+-K+ pump concentration gradient to drive the transport of glucose against its concentration gradient