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Lipid Bilayer as a Barrier
Core = hydrophobic fatty acid tails
Acts as an energy barrier to:
Charged species (Na⁺, K⁺, Cl⁻)
Polar molecules
Permeability Ranking
Highest → Lowest permeability:
Small nonpolar (O₂, CO₂)
Small uncharged polar (urea, ethanol)
Large uncharged polar (glucose)
Ions (Na⁺, K⁺, Ca²⁺) almost impermeable
Reason:
Ions require desolvation → extremely energetically costly
Free Energy of Transport (ΔG)
For ions:
ΔG = RTln([ion]in/[ion]out) + zFΔψ
Terms:
RT ln(...) → chemical gradient (ΔGc)
zFΔψ → electrical gradient (ΔGe)
Interpretation:
ΔG < 0 → spontaneous (down gradient)
ΔG > 0 → requires energy (active transport)
Electrochemical gradient = total driving force
membrane potential origin
Unequal distribution of ions
Selective permeability (especially K⁺)
If membrane permeable only to K⁺
K⁺ diffuses out (high → low)
Leaves behind negative charge
Creates electrical gradient pulling K⁺ back in
➡ Equilibrium reached when:
Electrical force = chemical force
Nernst Equation (Equilibrium Potential)
The equilibrium voltage for one ion:
Eion = (RT/zF) ln([ion]out/[ion]in)
Meaning
Voltage where net ion movement = 0
Each ion has its own equilibrium potential
Key Insight
If membrane permeable to one ion → membrane potential = that ion’s Nernst potential
Channel structure
Form continuous aqueous pore
Often highly selective (size + charge filter)
e.g. K⁺ channel excludes Na⁺ despite similar size
Based on hydration shell + pore geometry
Channel mechanism
No binding cycle required
Ions flow rapidly down gradient
Rate: up to 10⁸ ions/sec
No conformational change per ion
Channel gate types
Voltage-gated
Ligand-gated
Mechanically gated
Channel functional roles
Action potentials (Na⁺, K⁺)
Ca²⁺ signalling
Osmoregulation (Cl⁻ channels)
Carriers
Core Principle: Alternating Access Model
Binding site exposed:
First to one side
Then to the other
Never open to both sides simultaneously
~10²–10⁴ molecules/sec
Uniporters (Facilitated Diffusion)
Symporters
antiporters
Symporters + antiporters = secondary active transport
Energy source = ion gradient (NOT ATP directly)
Why are carriers slower than channels
Each cycle transports:
1–few molecules
Requires conformational change
Uniporters (Facilitated Diffusion)
Transport single molecule
Down concentration gradient
No energy input
Example:
GLUT1 (glucose uptake)
Symporters
Same direction transport
One solute moves:
Down gradient (driving ion)
Second solute:
Up gradient
Example
Na⁺ + glucose symporter:
Na⁺ gradient drives glucose uptake
Antiporters
Opposite directions
Example
Na⁺/Ca²⁺ exchanger:
Na⁺ in → Ca²⁺ out
Pumps (Primary Active Transport)
Use ATP hydrolysis:
ATP → ADP + Pi
Drives conformational changes
Key Property
Move ions against electrochemical gradient
Electrogenic: Unequal charge movement → voltage generated
Na⁺/K⁺ ATPase
Bind 3 Na⁺ (inside)
ATP phosphorylates pump
Conformational change → Na⁺ released outside
Bind 2 K⁺ outside
Dephosphorylation → returns to original state
K⁺ released inside
Net Effect
3 Na⁺ out / 2 K⁺ in
Creates:
Na⁺ gradient
K⁺ gradient
Negative membrane potential
Energy Coupling in Transport
Primary Active Transport
Direct ATP use
Secondary Active Transport
Uses stored energy in ion gradients
Energy Cascade
ATP → Na⁺ gradient → glucose uptake
Key Insight: Gradients are a form of stored energy
Animal Cell transport (Na⁺ Economy)
Central Pump
Na⁺/K⁺ ATPase
Why Na⁺?
Strong inward electrochemical gradient
Uses
Nutrient uptake (symport)
Ca²⁺ removal (antiport)
Electrical signalling
Key Point: Na⁺ gradient powers MANY processes
Plants & Fungi transport (H⁺ Economy)
Central Pump
H⁺ ATPase
Generates
Proton gradient + membrane potential
Uses
Nutrient uptake:
K⁺, phosphate, sulfate via H⁺ symport
Special Role
pH regulation
Salinity tolerance (Na⁺/H⁺ antiport)
Bacteria transport
No ATP pump for H⁺ initially
Instead:
Electron transport chain pumps H⁺
Uses
Nutrient uptake
ATP synthesis (chemiosmosis)
Endomembrane transport
V-type H⁺ Pumps
Acidify organelles
Functions
Vesicle loading (neurotransmitters)
Waste storage (vacuoles)
Electrogenic
Net charge movement
Alters membrane potential
Electroneutral
No net charge change
Transport Rates vs Abundance
Channels
Fast → few needed
Pumps
Slow → many required
Gradient dissipation (channels/carriers) > gradient generation (pumps)
Therefore:
Pumps must be abundant
Amino Acid Uptake
Na⁺/K⁺ pump:
Uses ATP
Creates Na⁺ gradient
Na⁺ gradient:
Drives symporter
Symporter:
Imports amino acids
Conclusion: Transport systems work together, not independently
Channel vs Transporter vs Pump
Channels:
Fast
Passive energy
Pore
Transporter:
Medium
Passive/secondary energy
Conformational
Pump:
Slow
ATP
Conformational