Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
116 Cards in this Set
- Front
- Back
- 3rd side (hint)
Being polar on one end and non-polar on the other is...
|
amphipathic
|
ex: detergents, cholesterol, phosphatidylcholine
|
|
what is a fatty acid?
|
aliphatic and amphipathic, can be saturated or unsaturated, have a hydroxyl head with a hydrocarbon chain
|
|
|
what is a triglyceride?
|
esters of fatty acids with glycerol, hydrophobic
|
|
|
what are sphingolipids?
|
Lipids with a variety of carbohydrates attached
|
|
|
what is a phospholipid?
|
Like triglycerides but the third position of glycerol has a phosphate attached with a polar head group attached through a phosphodiester bond.
They are amphipathic |
|
|
what are the 2 ways to synthesize phospholipids?
|
activate the head group first or the diacylglycerol first
|
|
|
what are 4 functions of phospholipids?
|
1.Membrane components
2. signaling molecules 3.surfactant 4.platelet activating factor |
|
|
what are 2 signaling functions of phospholipids?
|
phosphotidylinositides and aracidonic acid metabolism
|
|
|
How does phosphatidylinositol make DAG and IP3?
|
PI is phosphorylated by PI kinase into PIP, this is then phosphorylated by PIP kinase into PIP2, the PIP2 is hydrolyzed by PLC into DAG and IP3
|
|
|
what is surfactant?
|
phospholipids and proteins
|
|
|
what makes up a cholesterol?
|
polar head, steroid nucleus and alkyl side chain
|
|
|
Describe the steps in cholesterol synthesis?
|
3 acetyl CoA's combine, then the rate limiting step(reduction) makes mevalonate, 3 phosphate groups are added to make isoprene, then 6 activated isoprenes make squalene, this is cyclized to cholesterol
|
|
|
what are the different lipid transport molecules called?
|
chylomicrons
VLDL's IDL's LDL's HDL2 and 3 |
|
|
How is cholesterol disposed?
|
By bile acids or free cholesterol
|
|
|
what do cholystyramines do?
|
bind to bile acids and prevent reabsorption
|
|
|
what are eicosanoids?
|
prostaglandins and related compounds
|
|
|
What are the functions of Apo A,B,C and E?
|
A=activation of LCAT(to esterify the cholesterol)
B=receptor binding C=LPL activator(to transfer lipids) E=remenant receptor binding |
|
|
what makes corticosteroids anti-inflammatory?
|
prevent inducible Phospholipase A2 expression, reducing arachidonate release
|
|
|
What are highly specialized proteins with extraordinary catalytic power and a high degree of specificity for substrates?
|
Enzymes
|
|
|
inorganic ions required by some enzymes for catalytic action
|
cofactors
|
|
|
complex organic or metallo-organic molecules required by some enzymes for catalytic action
|
coenzymes
|
|
|
coenzyme or metal ion covalently bound to enzyme
|
prosthetic group
|
|
|
the complete catalytically active enzyme complex along with the bound coenzyme
|
holoenzyme
|
|
|
catalytically inactive protein part of the enzyme without the prosthetic group
|
apoenzyme/apoprotein
|
|
|
area on enzyme containing the amino acid side chains that are involved in catalyzing the reaction.
|
active site
|
|
|
the molecule that is bound in the active site and is acted on by the enzyme to form product.
|
substrate
|
|
|
what are the 2 distinguishing features of an enzyme catalyzed recation?
|
1. it only takes place within the active site
2.the molecule bound selectively and acted upon by the enzyme is the substrate |
|
|
the starting point for either a forward or reverse chemical reaction
|
ground state
|
|
|
when the molecules raised to a higher energy level reach the top of the energy hill, there is a point at which decay to the S or P state is equally probable.
|
transition state
|
|
|
the difference between the energy levels of the ground state and the transition state
|
activation energy
|
|
|
a higher activation energy corresponds to a (faster/slower) reaction?
|
slower
|
|
|
2 ways reaction rates can be increased?
|
1. increase temp
2.lowering activation energy |
|
|
what is the rate limiting step in a reaction?
|
the one with the highest activation energy
|
|
|
how do enzymes contribute to life?
|
selectivity and efficiency of reactions
|
|
|
what is binding energy?
|
energy released when substrate binds to active site in formation of ES complex
|
|
|
what is the major source of lowering activation energy?
|
binding energy
|
|
|
molecular agents that
interfere with catalysis, slowing or halting enzymatic reactions. |
enzyme inhibitor
|
|
|
how does a competitive inhibitor interfer with a reaction?
|
it competes with the substrate for the active site, it is overcome by adding more substrate(reversible)
|
|
|
how does a non-competitive inhibitor interfer with a reaction?
|
it binds covalently(irreversibly)or destroys a functional group in the active site, unable to be overcome by adding more substrate
|
|
|
a special class of irreversible
inhibitors. They are relatively un-reactive until they bind to the active site of a specific enzyme. |
suicide inactivator
|
|
|
what is maximum velocity?
|
the point at which all active sites are filled with substrate
|
|
|
what is Km?
|
the concentration of substrate that produces half max velocity
|
|
|
How does competitive inhibition affect Vmax and Km?
|
Vmax stays the same, Km is increased
|
|
|
How does non-competitive inhibition affect Vmax and Km?
|
Vmax is lowered and Km stays the same
|
|
|
Enzymes that undergo conformational changes
induced by the binding of modulators |
allostreic enzymes
|
|
|
what are allosteric modulators?
|
usually small metabolites or cofactors
|
|
|
what are homo/heterotropic regulatory enzymes?
|
homo=substrate and modulator are the same
hetero=substrate and modulator are different |
|
|
what is feedback inhibition?
|
when the end product of a reaction inhibits(turns off) regulatory enzymes
|
|
|
what are 2 ways of modulating regulatory enzymes?
|
1. reversible non-covalent binding of modulators(allosteric enzymes)
2. reversible covalent modification(phosphoralation) |
|
|
what is the function of protein kinases?
|
attach phosphoryl group to amino acid residue on regulatory enzyme(the glue)
|
|
|
what is the function of protein phosphatases?
|
removes the phosphoryl group from the regulatory enzyme(the scissors)
|
|
|
what is the difference between a micelle, bilayer and liposome?
|
micelle is single layer lipid "tube", liposome is a bilayer lipid "tube" which entraps water in the center of the tube
|
|
|
Glycerol molecule with a phosphate esterified at the a-carbon with two long-chain fatty acids
|
glycerophospholipids
|
|
|
carbohydrates that attach to proteins to form glycoproteins
|
membrane carbohydrates
|
|
|
what are the 3 major lipid components of eukaryotic membranes?
|
glycerophospholipids, spingolipids, cholesterol
|
|
|
what are 4 ways that phospholipids move?
|
1. lateral diffusion
2. hydrocarbon chain flexing 3. rotational diffusion 4. transverse exchange |
|
|
what promotes the transverse movement of lipids from one layer to another?
|
lipid transporter
ex:flippase |
|
|
List 6 examples of things that can affect lipid fluidity
|
1. temperature
2. phospholipid composition 3. head size/charge 4. cis double bond 5. cholesterol 6. fatty acid length |
|
|
These membrane proteins have sequences of hydrophobic amino acids, which create hydrophobic domains that interact with the hydrophobic hydrocarbons of the lipids and stabilize the protein–lipid complex. They need a detergent or organic solvent to be released from the membrane.
|
integral/intrinsic proteins
|
|
|
These proteins are released by treatment with salt solutions of different ionic strength or extremes of pH and are typically water soluable
|
peripheral/extrinsic proteins
|
|
|
what is the difference between a channel and a pore for facilitated movement through a membrane?
|
pores are non-selective for inorganic and organic molecules but channels are selective for inorganic anions and cations
|
|
|
an area of varying size where the plasma membranes of neighboring cells are separated and can open and close
|
gap junction
|
|
|
how is a pore formed?
|
Alignment of connexons from each cell across the gap junction. several cells combine to form the pore
|
|
|
hormonal stimulation of one cell can lead to signal propagation to a cluster of cells.
|
metabolic coupling through gap junctions
|
|
|
Depolarization of one group of muscle cells rapidly spreads to adjacent cells
|
electrical coupling through gap junctions
|
|
|
How does a voltage gated channel work?
|
voltage gated channels sense electrical gradients and selectively filter based on amino acid residues lining the channle area and the size of the open area
|
|
|
How does a ligand gated channel work?
|
when the receptor sites are occupied, the channel opens allowing diffusion of ions
|
|
|
How do membrane transporters work?
|
they physically bind to a molecule and carry it across the membrane
|
|
|
What is the difference between facilitated and active transport?
|
facilitated transport occurs passively down a gradient and active transport requires energy to move the solute
|
|
|
How does uniport differ from symport and antiport?
|
symport and antiport are cotransporters, symport requires the solute to be carried along with another molecule and antiport requires an exchange of molecules, uniport moves solute alone across the membrane
|
|
|
How do primary and secondary active transport differ?
|
primary transport moves a solute across one membrane either in or out of the cell, secondary transport moves the solute through the cell via 2 separate membrane transporters
|
|
|
what is group translocation?
|
when molecules such as amino acids are modified in order to transport across the membrane, large energy expenditures required
|
|
|
List 5 functions of lipids
|
1. energy source
2.structural components of cell membranes 3. chemical messengers 4.vitamin absorption and transportation 5. shock absorber to protect organs and insulate from temp extremes |
|
|
How do saturated and unsaturated fatty acids differ structurally?
|
saturated FA's are straight and unsaturated FA's have a kink in the chain
|
|
|
What are the 4 products in phosphatidylcholine synthesis?
|
1.choline
2. phosphocholine 3. CDP-choline 4. phosphatidylcholine |
|
|
What are the enzymes that act on the 4 products during phosphatidylcholine sysnthesis?
|
1. choline kinase
2. CTP choline cytidylyl transferase 3.CDP-choline diacylglycerol phosphocholine transferase |
|
|
Which kind of fatty acid has greater fluidity, saturated or unsaturated?
|
unsaturated
|
|
|
What does IP3 do?
|
activates the ligand gated Ca channel for slow release of Ca
|
|
|
What does DAG do in the cytosol?
|
combines with Ca released by IP3 to activate protein kinase C
|
|
|
How is PAF(platelet activating factor) made?
|
sysnthesized and released from activated immune cells
|
|
|
Where are the receptors for PAF?
|
on the lipid layer of the cell
|
|
|
How does PAF work?
|
it activates PLC and PLA2 and can aggregate platelets
|
|
|
What is the precursor to all steroid hormones except estradiol?
|
cholesterol
|
|
|
In what form is most of the cholesterol in the body?
|
cholesterol esters
|
|
|
Why is cholesterol esterified?
|
to help in transport between cells so it isn't taken back up by the cell it came from
|
|
|
Where does cholesterol synthesis take place?
|
in the liver
|
|
|
Where do statins work?
|
at the rate limiting step, HMG Co-A reductase conversion to mevalonate
|
|
|
Which is the largest cholesterol transport mechanism?
|
chylomicrons
|
|
|
Where are each of the following made?
chylomicrons, VLDL, LDL, HDL |
chylomicrons-small intestines
VLDL-liver LDL-from IDL(which is made from VLDL degredation) HDL-liver and intestine |
|
|
What is the primary function of each of the following?
chylomicron, VLDL, LDL, HDL |
chylomicron-transport dietary lipids
VLDL-transport endogenous triglycerides LDL-cholesterol transport HDL-reverse cholesterol transport |
|
|
Which apoprotein does HDL have that the others do not and what is it's function?
|
Apo A, it activates LCAT to esterify the cholesterol so it can't move back into the tissue cell it was taken from
|
|
|
How are LDL's removed from the blood?
|
bind to apo b recpetor site and taken into cell by endocytosis. Broken down by lysosome into AA's FA's cholesterol droplets and the receptor and are recycled.
|
|
|
How are apo B receptors synthesized?
|
by the ER of the cell, packaged by golgi and transported to surface for use
|
|
|
Which is the "bad" cholesterol for CV health, LDL or HDL?
|
LDL
|
|
|
What are 2 ways to lower total cholesterol?
|
statins (decrease synthesis)and cholysteramines(increase removal)
|
|
|
What effect does insulin and glucagon have on cholesterol synthesis?
|
insulin actiavtes while glucagon inactivates the HMG Co-A reductase in cholesterol synthesis, therefore, insulin=increase cholesterol
glucagon=decrease cholesterol |
|
|
What effect does free cholesterol levels have on cholesterol regulation?
|
higher free cholesterol levels (in the cell)
1.inhibit ACAT (enzyme)formation of cholesterol esters 2. inhibit uptake of cholesterol from extracellular sources 3. feedback inhibition of HMG Co-A reductase in synthesis of new cholesterol |
|
|
Why are ecosinoids considered "local hormones"?
|
They act on target cells close to their site of formation and they are broken down quickly so they do not travel far.
|
|
|
prostaglandins, thromboxanes, and leukotrienes are all...
|
eicosanoids
|
|
|
What is PLA2's role in the synthesis of eicosinoids?
|
it cleaves the AA from the membrane phospholipid
|
|
|
What is the impulse conduction on a myelinated sheath called?
|
saltatory conduction
|
|
|
What does the nernst equation defune?
|
The relation of the diffusion potential to the concentration difference of an ion
|
|
|
What does propagate mean?
|
conducted without reduction
|
|
|
What are characteristics of action potentials?
|
1. all or nothing events
2. constant amplitude 3. initiated by depolarization 4.involve changes in membrane permeability 5. rely on voltage gated channels |
|
|
What state are the channels in during resting membrane potential?
|
the activation gates are closed and the inactivation gates are open
|
|
|
What state are the channels in during depolarization?
|
voltage gated Na channels are open and voltage gated K channels start to open
|
|
|
what state are the channels in during repolarization?
|
voltage gated Na channels are closed and voltage gated K channels are open
|
|
|
What state are the channels in during end repolarization and afterpotential?
|
voltage gated Na channels are closed, diffusion of K produces afterpotential
|
|
|
Can a action potential initiate depolarization during the absolute refractory period?
|
No
|
|
|
How does action potential depolarization during the relative refractory period affect the threshold?
|
lower threshold until after relative refractory period is complete
|
|
|
List 4 functions of action potentials?
|
1. info delivery to CNS
2. info encoding 3. rapid transmission over distance 4. initiators of cellular responses in non-nervous tissue |
|
|
What makes perkinjie and pacemaker cells different from nerve cells related to action potential?
|
They rely on Ca channels asopposed to Na channels for their action.
|
|
|
What channels are located in the subneural cleft of a NMJ?
|
Ach gated channels at the top and voltage gated Na channels on the bottom
|
|
|
Describe the 4 steps in transmission of action potential at NMJ motor end plate.
|
1. action potential causes voltage gated Ca channels to open
2. Ca in presynaptic terminal causes release of Ach 3. Diffusion of Ach to post-synaptic muscle fiber causing inc permeability of ligand gated Na channels 4. Na permeability results in depolarization |
|
|
What happens to Ach after it's use on post-synaptic receptors?
|
AchE breaks it down and the choline is taken back up by pre-synaptic cell to be recycled into more Ach
|
|
|
What is the function of Mg on the RYR1 receptor?
|
Mg attached to high and low affinity binding sites keeps Ca channels closed
|
|