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The cell membrane isn't just a passive barrier—it's the gatekeeper that determines what enters and exits every living cell. On the AP Biology exam, you're being tested on your understanding of selective permeability, concentration gradients, electrochemical gradients, and how cells use energy to maintain internal conditions different from their environment. These concepts connect directly to Unit 2 (Cell Structure) and cascade into Unit 4 (Cell Communication), where membrane transport underlies everything from nerve impulses to hormone signaling.
Think of transport mechanisms as existing on a spectrum from "no energy required" to "significant ATP investment." The exam loves to test whether you can identify which mechanism applies to a given scenario and why that mechanism is necessary. Don't just memorize that the sodium-potassium pump uses ATP—know that it moves ions against their concentration gradient, which is thermodynamically unfavorable without energy input. Master the underlying principles, and you'll be ready for any FRQ that throws a novel transport scenario your way.
Passive transport mechanisms share one fundamental principle: molecules move spontaneously from regions of high concentration to low concentration, driven by the second law of thermodynamics. No ATP required—the concentration gradient itself provides the driving force.
Compare: Simple diffusion vs. facilitated diffusion—both are passive and move molecules down concentration gradients, but facilitated diffusion requires protein assistance and shows saturation. If an FRQ asks why glucose transport plateaus at high concentrations, saturation of carrier proteins is your answer.
Active transport mechanisms share the requirement for energy input because they move substances against their concentration or electrochemical gradient. This is thermodynamically unfavorable—like pushing a boulder uphill—and requires ATP hydrolysis or coupling to another gradient.
Compare: Sodium-potassium pump vs. ion channels—the pump uses ATP to create the gradient; channels allow ions to flow down that gradient passively. Both are essential for action potentials, but they serve opposite functions in maintaining vs. dissipating the electrochemical gradient.
When molecules are too large to pass through channels or carriers, cells use membrane-bound vesicles to transport them. These processes require ATP for membrane remodeling and vesicle movement along the cytoskeleton.
Compare: Endocytosis vs. exocytosis—both use vesicles and require energy, but they move materials in opposite directions. Endocytosis brings material in (membrane area decreases); exocytosis releases material out (membrane area increases). Neurotransmitter release is the classic exocytosis example for FRQs.
| Concept | Best Examples |
|---|---|
| Passive transport (no ATP) | Simple diffusion, facilitated diffusion, osmosis |
| Crosses membrane without proteins | , , (small nonpolar molecules) |
| Requires transport proteins | Glucose transport, ion channels, aquaporins |
| Primary active transport | Sodium-potassium pump (-ATPase) |
| Electrochemical gradient | Ion channels, sodium-potassium pump, action potentials |
| Bulk transport (vesicles) | Endocytosis, exocytosis, vesicular trafficking |
| Saturation kinetics | Facilitated diffusion, carrier proteins |
| Membrane remodeling | Phagocytosis, pinocytosis, SNARE-mediated fusion |
Both facilitated diffusion and the sodium-potassium pump use membrane proteins. What is the fundamental difference that determines whether ATP is required?
A cell is placed in a hypertonic solution. Using your knowledge of osmosis, predict what will happen to a plant cell versus an animal cell—and explain why their fates differ.
Compare and contrast ion channels and carrier proteins: How do their mechanisms differ, and why might a cell use one over the other?
If an FRQ describes a neuron that cannot maintain its resting membrane potential, which transport mechanism has most likely failed? Explain how this failure would affect the cell's ability to generate action potentials.
Identify two transport mechanisms that exhibit saturation kinetics. What molecular feature do they share that explains this limitation?