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2.8Cells

Mechanisms of Transport — AP BIOLOGY Revision Notes & Topical Questions

5 min read 12 parts Lesson 10 of 12 1 quiz

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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

TypeDescriptionExample
Phagocytosis (cell eating)The cell extends pseudopodia round a large particle and engulfs it in a vacuole that fuses with a lysosomeWhite blood cells engulfing bacteria; Amoeba feeding
Pinocytosis (cell drinking)The cell takes in droplets of extracellular fluid and dissolved substances nonspecifically in small vesiclesAbsorption by many cells, such as kidney cells
Receptor-mediated endocytosisSpecific molecules bind to receptors concentrated in coated pits, which pinch into vesiclesUptake 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

TermMeaning
ExocytosisRelease of material by vesicle fusion.
EndocytosisUptake by membrane infolding.
PhagocytosisCell eating; uptake of large particles.
PinocytosisCell drinking; uptake of fluid.
Receptor-mediated endocytosisSpecific uptake via receptors, such as LDL.
CotransportSecondary active transport driven by an ion gradient.
SymportTwo substances move in the same direction.
AntiportTwo substances move in opposite directions.
VesicleA 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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