Membrane Transporters Flashcards
What kinds of molecules can freely diffuse across the plasma membrane?
- hydrophobic molecules
- some gases
- steroid hormones
Ion Channels
Specificity/Speed/Direction
- low specificity (will let different ions through)
- ions move downhill gradient
- NO ENERGY REQUIRED
Ion Carriers
Specificity/Speed/Direction
- intermediate specificity
- ions move downhill gradient
- NO ENERGY REQUIRED
Ion Pumps
Specificity/Speed/Direction
- absolute specificity
- ions move uphill gradient
- ATP REQUIRED
Ion Channels are:
- ion-specific pores that open and close in a regulated manner
- passive transport (no energy required)
Ion carriers are:
- enzyme-like proteins that mediate passive transport down concentration gradients without chemical change
- passive transport (no energy)
Ion pumps are:
- enzymes that need energy to move ions and other solutes across the membrane against a concentration gradient
- energy provided via ATP-mediated phosphorylation or ATP binding and hydrolysis
Membrane potential and ion transport:
- combines with concentration gradient to form the electrochemical gradient
- membrane potential can either support or oppose ions moving with their concentration gradient.
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Ion channels are critical to the function of what types of tissues?
- nerve and muscle
- dependent on K+, Na+, Ca2+ channels
Ion channels can reject ions on the basis of:
- wrong charge
- wrong size
note: ion channels have low specificity overall
Toxins that can block ion channels:
- tetrodotoxin (Na+ channels)
- lidocaine (Na+ channels)
- scorpion/snail poison (K+ channels)
- Nicotine (acetylcholine channels)
What are the three major “carrier-type” transporters?
- uniport
- symport (coupled transport)
- antiport (coupled transport)
Uniport Ion Carriers:
- transport a single ion down its concentration gradient.
- passive transport (no energy)
- rate dependent on concentration gradient
- binding affinity-similar to enzyme kinetics
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Na+/glucose symport ion carrier:
- co-operative transport.
- transports one ion down its concentration gradient along with another ion against its concentration gradient.
- passive transport (no energy)
- co-operative binding
- will not function unless both substrates bound.
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Epithelial cell polarity can be maintained due to:
- the presence of tight junctions
- do not allow membrane proteins to diffuse around membrane.
- cause non-random distribution of membrane transporter proteins.
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Steps in transcellular glucose transport from digestive system through epithelial cell:
- Symporter moves Na+ with its gradient and glucose against its gradient from the intestinal lumen through the apical region of epithelial cell.
- Glucose moves down its gradient through a uniporter on the basal side of the epithelial cell.
- Na+/K+ pump on basal side of epithelial cell maintains Na+ levels in epithelial cell.
P-type ion pumps:
- ATP-driven pumps
- autophosphorylate themselves with ATP, which results in a conformational change
- multi-pass transmembrane domains
- pumps ions
ABC transporter:
- ATP-driven pump
-
pumps small molecules
- such as drugs
Ca2+ ATPase:
- p-type ATP-driven ion pump
- 90% of membrane protein in muscle cells
- moves calcium against its concentration gradient
Steps in Ca2+ ATPase activity:
- Cavity in non-phosphorylated transporter binds calcium.
- ATP binds and contributes phosphate for phosphorylation.
- When aspartate phosphorylated, conformational change occurs.
- Opens channel to lumen of sarcoplasmic reticulum and releases Ca+2
Na+/K+ ATPase:
- p-type ATP-driven ion pump
- 1/3 of cellular energy used to maintain this pump
- ATP causes a conformation change in the transporter that moves Na+/K+ both against their concentration gradients.
ABC Transporters (General Information):
- ATP-binding casettes
- Two ATPase domains on each transporter
- abundant in bacteria
- present in eukaryotes
Steps in ABC Transport:
- small molecule binds to non-ATP bound state.
- ATP binds to both ATPase binding domains.
- ATPase binding domains dimerize to produce a conformational change that exposes substrate to opposite side of membrane for release.
- ATP hydrolysis releases substrate, then prepares transporter for another round of transport.
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ABC transporters in humans are important for:
- multiple drug resistance
- tumor cells overexpress ABC transporter that pumps chemo-drug out.
- chloroquine resistance
- malaria induces cells to overexpress ABC transporter that pumps malaria-drug out.
- cystic fibrosis
- ATP binding to ABC transporter can cause it to become a channel for chlorine