Passive transporters move solutes along electrochemical gradients (e.g., glucose transporter).
Electrical component of glucose's electrochemical gradient
Glucose is uncharged, relies on concentration gradient.
Glucose transporter: random conformational switching
Binding site alternates between exterior and interior of the cell.
Blood glucose regulation through import/export mechanisms.
Pumps transport solutes against their electrochemical gradients:
ATP-driven pumps: Utilize ATP hydrolysis energy for uphill transport.
Gradient-driven pumps: Use downhill transport of one solute for uphill transport of another.
Light-driven pumps: Harness energy from sunlight.
The Na+ pump uses ATP hydrolysis to transport:
3 Na+ out
2 K+ in
Benefits of coupling two ions:
Prevents energy loss during ATP hydrolysis.
Maintains cytosolic low Na+ and high K+ concentrations.
Cycle dependent on sequence of steps; if one fails, the whole cycle halts.
Effect of ouabain: halts pump by preventing K+ binding.
Na+-K+ pump generates a steep Na+ concentration gradient.
Conceptualize this gradient as energy storage, analogous to water behind a dam.
Ca2+ pumps maintain low cytosolic Ca2+ similar to Na+-K+ pumps.
Both are ATPases with similar amino acid sequences.
Key difference: Ca2+ pump does not require a secondary ion for operation.
Gradient-driven pumps utilize energies:
Symport: Moves two solutes in the same direction.
Antiport: Moves solutes in opposite directions.
Uniport: Moves one type of solute (not a pump).
Glucose transport from gut lumen to blood via symport, regardless of high intracellular concentration.
Driven by the electrochemical Na+ gradient for active import of glucose.
Cooperative binding: enhances transport efficiency.
Prevents Na+ leakage when glucose is absent.
Different transporters are localized at apical and basal sides of cells.
Glucose symport on the apical side; glucose uniport on the basolateral.
Uniport releases glucose into bloodstream, aiding in regulation of glucose distribution.
Light-driven pumps (e.g., bacteriorhodopsin) generate H+ gradients in some bacteria.
Question regarding how ouabain impacts glucose transport on the apical membrane:
Possible outcomes addressed (options A-D) regarding glucose transport dynamics.
K+ leak channels and Na+-K+ pump critical for resting membrane potential.
Na+-K+ pump maintains Na+ low and K+ high in cytosol.
K+ leak contributes to negative membrane potential.
K+ moving down its concentration gradient faces electrical gradient opposition.
Equilibrium set when K+ concentration gradient balances the membrane potential.
Variation in resting membrane potential (-20 to -200 mV).
K+ leak channels selectively permit K+ ions.
Na+ ions, though smaller, cannot pass due to channel structure specifics, favoring K+ interactions.
Ion channels change between open/closed states randomly.
Patch clamp technique used to measure ion flow in isolated membrane patches.
Gated mechanisms regulate ion channel states based on:
Voltage changes (voltage-gated channels)
Ligand binding (ligand-gated channels)
Mechanical forces (mechanically-gated channels)
Mechanical stimulation opens channels in auditory hair cells.
Stereocilia movement from sound vibrations initiates channel opening, allowing ion influx.