Movement of Substances Through Membranes

Chapter 6 · Pre-Medical Biology · Dr. Soltani
Root
Permeability
Passive Transport
Active Transport
Vesicular Transport
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🧬 Membrane Transport
Movement of Substances Through Membranes
🔬 Membrane Permeability
🚫 Impermeable — complete barrier, nothing crosses in either direction
✅ Freely Permeable — all substances cross freely (not compatible with life)
⚖️ Selectively Permeable — cell membranes use THIS: size · charge · lipid solubility i
Selective permeability is the basis of ALL transport mechanisms. The three selection criteria are: (1) Molecular size — smaller crosses easier, (2) Electric charge — charged ions are repelled by the hydrophobic core, (3) Lipid solubility — nonpolar molecules dissolve in the bilayer and cross freely.
⛰️ Passive Transport
💨 Simple Diffusion
🧱 Crosses lipid bilayer directly — no membrane protein needed
⚗️ Only small nonpolar molecules: O₂ · CO₂ · fatty acids · steroid hormones · H₂O
❌ Cannot cross: Na⁺ · K⁺ · Cl⁻ · Glucose · Amino acids (polar/charged)
📐 4 Factors affecting rate: Temperature · Molecule size · Medium density · Concentration gradient i
↑ Temperature → faster kinetic energy → faster diffusion. ↑ Molecule size → slower. ↑ Medium density → slower. ↑ Concentration gradient → faster net flux toward equilibrium.
💧 Osmosis
🌊 Water diffusion: HIGH [H₂O] → LOW [H₂O] (toward more solute)
📊 Osmolarity = total dissolved particles: Glucose=1 · NaCl=2 · MgCl₂=3 osmol/L i
NaCl dissociates into Na⁺ + Cl⁻ = 2 particles per molecule. MgCl₂ → Mg²⁺ + 2Cl⁻ = 3 particles. Higher osmolarity = more dissolved particles = less free water.
💪 Osmotic Pressure — force resisting water entry (used in clinical settings)
Tonicity: Isotonic = normal shape (0.9% NaCl) · Hypotonic = cell swells/bursts · Hypertonic = cell crenates
🚪 Facilitated Diffusion
〰️ Channel Mediated
🔑 Ligand-gated — channel opens when specific molecule binds
⚡ Voltage-gated — channel opens with membrane electrical change
🧪 Ion passage: Na⁺ · K⁺ · Cl⁻ · Ca²⁺ (electrochemical gradient driven)
🔄 Carrier Mediated
🎯 Specific Binding — one substrate type per carrier protein
🔃 Shape Change — conformational transition carries substrate across
📈 Saturation Point — maximum rate when all carriers occupied
🍬 Glucose via GLUT carriers — passive entry into most cells i
GLUT (Glucose Transporter) carriers allow glucose to enter most body cells passively — down the glucose gradient. Glucose is metabolized immediately, keeping intracellular levels low and ensuring continuous inward flux. Exception: intestines and kidneys use ACTIVE transport for glucose uptake.
⚡ Active Transport
🔋 Primary Active Transport
⚡ ATP Hydrolysis — direct energy from ATP powers the pump (ATPase)
🔁 Na⁺/K⁺ ATPase Pump
3 Na⁺ pumped OUT — against gradient (per cycle)
2 K⁺ pumped IN — against gradient (per cycle)
1 ATP consumed per pump cycle
⚡ Electrogenic → creates −70 mV resting membrane potential i
3 positive charges out vs 2 in = net negative inside. This −70 mV resting membrane potential is the foundation of all nerve impulses and muscle contraction. Nerve cells spend 70% of their energy on this pump alone.
Na⁺: ICF ~15 mEq/L (LOW) ↔ ECF ~142 mEq/L (HIGH)
K⁺: ICF ~150 mEq/L (HIGH) ↔ ECF ~5 mEq/L (LOW)
Ca²⁺: ICF ~0.0001 mEq/L (VERY LOW) ↔ ECF ~2.4 mEq/L (HIGH)
📡 Ca²⁺ ATPase Pump
Pumps Ca²⁺ OUT of cytoplasm (plasma membrane · ER · mitochondria)
Cytoplasmic Ca²⁺ kept extremely low: ~0.0001 mEq/L
Ca²⁺ rise = key signal → triggers muscle contraction, hormone secretion, exocytosis
⚗️ H⁺ ATPase Pump
Stomach parietal cells → secretes HCl (gastric acid)
Kidney tubules → acidifies urine
Mitochondria → H⁺ gradient drives ATP synthesis (oxidative phosphorylation)
🔗 Secondary Active Transport
⚡ Ion Gradients Energy — uses Na⁺ gradient stored by Na⁺/K⁺ pump (indirect ATP) i
No direct ATP used. Instead, the Na⁺ gradient created by the Na⁺/K⁺ pump acts as stored energy. Na⁺ flows down its gradient into the cell and this released energy drives a 2nd molecule uphill against its own gradient.
↓↓ Symport — SAME direction
🍬 Na⁺ + Glucose → BOTH into intestinal cells (absorption after digestion)
🧬 Na⁺ + Amino acids → BOTH in (same mechanism, different carrier)
🏥 SGLT2 Inhibitors — Diabetes drugs block Na⁺/glucose symport in kidney i
SGLT2 = the Na⁺/glucose symporter in kidney tubules that reabsorbs glucose from filtrate back to blood. Drugs empagliflozin, dapagliflozin, canagliflozin block it → glucose lost in urine → blood sugar falls. This is a direct clinical application of secondary active transport.
↓↑ Antiport — OPPOSITE direction
Na⁺ enters cell while Ca²⁺ is expelled simultaneously
Double safety: Ca²⁺ ATPase pump + Na⁺/Ca²⁺ antiport both maintain low cytoplasmic Ca²⁺
📦 Vesicular Transport
📤 Exocytosis — OUT of cell
① Package — cargo proteins packaged into secretory vesicles (Golgi apparatus)
② Migrate — vesicle travels along cytoskeletal filaments to plasma membrane
③ Fuse & Release — SNARE proteins mediate membrane fusion → contents released to ECF
Example: Insulin release from pancreatic β cells · Neurotransmitter release at synapses
📥 Endocytosis — INTO cell
💧 Pinocytosis — "Cell Drinking"
Small vesicle — takes in extracellular fluid + dissolved solutes
Occurs continuously in almost ALL eukaryotic cells
Function: nutrient intake, membrane recycling, ECF sampling
🦠 Phagocytosis — "Cell Eating"
Large phagosome — engulfs bacteria, viruses, cellular debris
ONLY in neutrophils and macrophages (specialized white blood cells)
🛡️ Innate immune defense: phagosome fuses with lysosomes → digestive enzymes destroy pathogen
⛰️ Passive Transport — No ATP
Simple Diffusion · Osmosis · Facilitated Diffusion
Direction: High → Low concentration
Spontaneous — like a ball rolling downhill
⚡ Active Transport — ATP Required
Primary (direct ATP) · Secondary (Na⁺ gradient)
Direction: Low → High concentration (uphill)
Requires specific pump or carrier proteins
📦 Vesicular Transport — Bulk
Exocytosis (out of cell) · Endocytosis (into cell)
For large cargo — proteins, bacteria, whole particles
Membrane vesicles carry the cargo
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