2.8Cells
Mechanisms of Transport — AP BIOLOGY Revision Notes & Topical Questions
5 min read 12 parts Lesson 10 of 12 1 quiz
Lesson summary
2.8 Mechanisms of Transport — Notes — AP Biology notes: Describe the processes that allow ions and other molecules to move across membranes.Gradients — selective permeability allows solute concentration gradients to form, either because the membrane blocks a substance or because …
- Passive transport
- Rate of simple diffusion
- Active transport
- Metabolic poisons
- Electrogenic pumps
- Bulk transport
Section 1 of 12Introduction to membrane transport
Gradients
- Gradients selective permeability allows solute concentration gradients to form, either because the membrane blocks a substance or because proteins pump it to build a high concentration on one side
Factors deciding the mechanism
- The substance to be transported, whether small, large, polar or nonpolar.
- The concentration gradient across the membrane.
Mechanisms
- Mechanisms passive transport and active transport (including endocytosis and exocytosis)
- (diffusion, osmosis)
Section 2 of 12Passive transport
Passive transport
Passive transport the net movement of molecules from high to low concentration without direct input of metabolic energy
Types
- Simple diffusion moves molecules down a concentration gradient directly across the phospholipid bilayer.
- Facilitated diffusion moves molecules down a concentration gradient through specialised transport proteins.
- Osmosis moves water down a water potential gradient between the phospholipids or via aquaporins.
Rate of simple diffusion
- Rate of simple diffusion it increases with a steeper gradient, higher temperature, larger surface area and smaller molecules
Section 3 of 12Active transport
Active transport
Active transport the direct input of energy to move molecules from low concentration to high concentration
Energy
- Energy it uses ATP from respiration and always involves carrier proteins (pumps) across a membrane
Gradients
- Gradients it establishes and maintains concentration gradients, such as K⁺ high inside and Na⁺ high outside cells,
- which are essential for nerve impulses and cotransport
Metabolic poisons
- Metabolic poisons substances such as cyanide stop ATP production,
- so primary active transport stops and secondary active transport follows as gradients dissipate,
- while passive transport continues
Section 4 of 12Primary and secondary active transport
Primary and secondary active transport
Primary active transport
- Primary active transport it uses ATP directly to power a pump, such as Na⁺/K⁺ ATPase or proton pumps
Secondary active transport (cotransport)
- Secondary active transport (cotransport) it uses the energy stored in a gradient made by primary active transport to move another substance against its gradient
Direction
- Direction in symport both substances move in the same direction and in antiport they move in opposite directions
Examples
- The Na⁺–glucose cotransporter in intestinal cells moves Na⁺ down its gradient and glucose against its gradient into the cell,
- and glucose leaves into the blood by facilitated diffusion.
- In plants, proton pumps create an H⁺ gradient and H⁺–sucrose cotransporters load sucrose into the phloem.
Electrogenic pumps
- Electrogenic pumps pumps such as the proton pump generate voltage across membranes, storing energy for cellular work
Section 5 of 12Na⁺/K⁺ ATPase
1
Three sodium ions from inside the axon bind to the pump.
2
ATP attaches and transfers a phosphate to the pump, which changes shape and opens to the outside.
3
The three sodium ions are released outside the axon.
4
Two potassium ions from outside bind to their binding sites.
5
The phosphate is released, which changes the shape of the pump again.
6
The shape change releases the two potassium ions inside the axon.
Na⁺/K⁺ ATPase
Function
- Function the pump uses ATP to maintain sodium and potassium gradients and the membrane potential of nerve cells, so it supports nerve impulses
Ratio
- Ratio each cycle uses one ATP to pump 3 Na⁺ out and 2 K⁺ in
Section 6 of 12Exocytosis and endocytosis
Bulk transport
- Bulk transport large molecules, large amounts of substances, particles and even whole cells are moved in membrane-bound vesicles,
- which needs energy,
- so both processes are active transport
Exocytosis
- Exocytosis materials are transported out of the cell
- The substance is packaged into internal vesicles.
- The vesicles travel to the plasma membrane, fuse with it and release their contents outside the cell.
- Examples are neurotransmitter release, insulin secretion, digestive enzyme secretion and plant cell wall materials.
- The vesicle membrane becomes part of the plasma membrane, so exocytosis adds membrane to the cell surface.
Endocytosis
- Endocytosis the cell takes in large molecules and particles
- The plasma membrane folds in on itself and engulfs the material in a new vesicle.
- The vesicle carries the material into the cell.
Membrane balance
- Membrane balance membrane added by exocytosis is removed by endocytosis, so cell surface area stays roughly constant
Food vesicles
- Food vesicles they fuse with lysosomes, whose enzymes digest the contents and the products enter the cytoplasm
Recycling
- Recycling vesicles carrying receptors may be recycled back to the surface
Section 7 of 12Types of endocytosis
| Type | Description | Example |
|---|---|---|
| Phagocytosis (cell eating) | The cell extends pseudopodia round a large particle and engulfs it in a vacuole that fuses with a lysosome | White blood cells engulfing bacteria; Amoeba feeding |
| Pinocytosis (cell drinking) | The cell takes in droplets of extracellular fluid and dissolved substances nonspecifically in small vesicles | Absorption by many cells, such as kidney cells |
| Receptor-mediated endocytosis | Specific molecules bind to receptors concentrated in coated pits, which pinch into vesicles | Uptake of cholesterol-carrying LDL by liver cells |
Types of endocytosis
Selectivity
- Selectivity in receptor-mediated endocytosis only molecules that bind the receptors enter, so substances in low concentration can be taken up
Disease
- Disease in familial hypercholesterolaemia the LDL receptors are faulty, so cholesterol is not taken up and blood levels rise
Section 8 of 12Vesicle traffic and the endomembrane system
Vesicle traffic and the endomembrane system
Endomembrane system
- Endomembrane system the movement of membrane by vesicles is the basis of the system, and cells with rapid secretion have extensive ER and Golgi
Directed traffic
- Directed traffic each vesicle carries identifying proteins and docking proteins on the target membrane recognise it,
- and botulinum toxin cuts fusion proteins and causes paralysis
Pulse-chase
- Pulse-chase radioactive amino acids given briefly showed the label in rough ER first, then the Golgi, then secretory vesicles and outside the cell
Section 9 of 12Examples of vesicle transport
Examples of vesicle transport
Nerve terminal
- Nerve terminal calcium entry triggers neurotransmitter vesicles to fuse with the presynaptic membrane, releasing acetylcholine into the cleft,
- and the membrane is retrieved by endocytosis
Digestive and immune systems
- Digestive and immune systems intestinal cells take up fat droplets, the pancreas releases enzymes by exocytosis, macrophages engulf pathogens and plasma cells export antibodies
Plants
- Golgi vesicles carry cell wall materials and membrane to the surface and to the growing cell plate
Protists
- Protists food vacuoles form by phagocytosis and combine with lysosomes
Pathogens
- Pathogens viruses bind receptors and enter by receptor-mediated endocytosis, so blocking the receptor can prevent infection
Section 10 of 12More from the specification
Hydrophobic
- Water-hating; non-polar and unable to dissolve in water.
Tonicity
- The ability of a solution to change the water content of a cell.
Hydrophilic
- Water-loving; polar or charged and able to dissolve in water.
Pressure potential
- Physical pressure on a solution.
Section 11 of 12Key terms
| Term | Meaning |
|---|---|
| Exocytosis | Release of material by vesicle fusion. |
| Endocytosis | Uptake by membrane infolding. |
| Phagocytosis | Cell eating; uptake of large particles. |
| Pinocytosis | Cell drinking; uptake of fluid. |
| Receptor-mediated endocytosis | Specific uptake via receptors, such as LDL. |
| Cotransport | Secondary active transport driven by an ion gradient. |
| Symport | Two substances move in the same direction. |
| Antiport | Two substances move in opposite directions. |
| Vesicle | A membrane-bound sac that carries materials. |
Section 12 of 12Exam technique
1
Saying bulk transport needs no energy — it uses ATP.
2
Confusing symport (same direction) with antiport (opposite directions).
3
Thinking cotransport uses ATP directly — it uses a gradient made by a pump.
4
Saying a metabolic poison stops passive transport — it only stops transport that needs ATP.
5
Thinking vesicles pass through the membrane — they fuse with it or form from it.
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