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๐Ÿ”ฌBiophysics Unit 7 Review

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7.1 Passive diffusion and facilitated transport

๐Ÿ”ฌBiophysics
Unit 7 Review

7.1 Passive diffusion and facilitated transport

Written by the Fiveable Content Team โ€ข Last updated September 2025
Written by the Fiveable Content Team โ€ข Last updated September 2025
๐Ÿ”ฌBiophysics
Unit & Topic Study Guides

Passive diffusion and facilitated transport are crucial mechanisms for moving molecules across cell membranes. These processes rely on concentration gradients, allowing substances to flow from high to low concentrations without energy input.

While passive diffusion lets small, nonpolar molecules pass through the membrane directly, facilitated transport uses proteins to help larger or charged molecules cross. Both methods play vital roles in cellular function, nutrient uptake, and waste removal.

Passive Diffusion: Principles and Role

Fundamentals of Passive Diffusion

  • Passive diffusion involves the movement of molecules from a region of high concentration to a region of low concentration, driven by the concentration gradient
  • This process occurs without the expenditure of cellular energy (ATP)
  • Molecules move down their concentration gradient until equilibrium is reached, at which point the net movement of molecules across the membrane is zero
  • The rate of passive diffusion is directly proportional to the steepness of the concentration gradient (a larger difference in concentration results in a faster rate of diffusion)

Passive Diffusion Across Cell Membranes

  • Passive diffusion occurs through the phospholipid bilayer of the cell membrane, allowing certain molecules to pass through without the aid of membrane proteins
  • Small, nonpolar molecules (oxygen, carbon dioxide, and certain lipid-soluble molecules like steroids) can easily diffuse through the hydrophobic core of the membrane
  • The permeability of the cell membrane to different molecules depends on their size, charge, and polarity
  • Larger, polar, or charged molecules have difficulty passing through the membrane via passive diffusion due to their incompatibility with the hydrophobic interior of the bilayer
  • Passive diffusion plays a crucial role in the transport of gases across the cell membrane, facilitating cellular respiration (oxygen uptake) and removal of metabolic waste (carbon dioxide release)

Facilitated Diffusion: Process and Significance

Mechanism of Facilitated Diffusion

  • Facilitated diffusion is a type of passive transport that involves the movement of specific molecules across the cell membrane with the help of membrane-bound proteins
  • Carrier proteins undergo conformational changes to bind and transport specific molecules across the membrane
    • Example: Glucose transporter (GLUT) proteins facilitate the uptake of glucose into cells
  • Channel proteins form hydrophilic pores that allow the passage of specific ions or small molecules
    • Example: Potassium ion channels allow the selective movement of K+ ions across the membrane
  • Facilitated diffusion enables the transport of larger, polar, or charged molecules that cannot easily pass through the phospholipid bilayer

Significance of Facilitated Diffusion in Biological Systems

  • Facilitated diffusion is essential for the uptake of nutrients by cells
    • Glucose and amino acid transporters ensure an adequate supply of these vital molecules for cellular metabolism and growth
  • Ion channels regulate the concentration of ions (sodium, potassium, calcium) across the membrane, crucial for maintaining the membrane potential and signal transduction
  • Facilitated diffusion aids in the removal of waste products from cells, such as the transport of urea out of liver cells
  • The rate of facilitated diffusion is limited by the number of available carrier or channel proteins and their saturation at high substrate concentrations
  • Saturation occurs when all the binding sites on the proteins are occupied, resulting in a maximum transport rate (Vmax) that cannot be exceeded even with further increases in substrate concentration

Passive Diffusion vs Facilitated Transport

Similarities

  • Both passive diffusion and facilitated diffusion are forms of passive transport that move molecules down their concentration gradient
  • Neither process requires the expenditure of cellular energy (ATP)
  • The rate of transport for both mechanisms is influenced by the concentration gradient (a steeper gradient leads to faster transport)

Differences

  • Passive diffusion occurs directly through the phospholipid bilayer, while facilitated diffusion requires the assistance of membrane-bound carrier proteins or channel proteins
  • Passive diffusion is limited to small, nonpolar molecules, whereas facilitated diffusion can transport larger, polar, or charged molecules
  • The rate of passive diffusion is directly proportional to the concentration gradient, while the rate of facilitated diffusion is limited by the number and saturation of carrier or channel proteins
  • Passive diffusion does not exhibit specificity for particular molecules, while facilitated diffusion is highly specific, with proteins transporting only certain molecules or ions

Factors Influencing Diffusion Rates

Concentration Gradient

  • The concentration gradient is a primary factor influencing the rate of both passive diffusion and facilitated transport
  • A steeper concentration gradient (a larger difference in concentration between the two sides of the membrane) results in a higher rate of molecular movement
  • As the concentration gradient decreases, the rate of diffusion or transport slows down until equilibrium is reached

Temperature

  • Temperature affects the rate of passive diffusion and facilitated transport by influencing the kinetic energy of molecules
  • Higher temperatures increase the kinetic energy of molecules, causing them to move faster and collide with the membrane more frequently
  • Consequently, higher temperatures generally increase the rate of diffusion and transport
  • Lower temperatures decrease kinetic energy and slow down the rate of diffusion and transport

Membrane Permeability and Composition

  • Membrane permeability, determined by the composition and structure of the phospholipid bilayer, influences the rate of passive diffusion
  • More permeable membranes allow for faster diffusion of molecules
  • The presence of cholesterol in the membrane can reduce permeability by increasing the rigidity of the bilayer and hindering the movement of molecules
  • The type and proportion of phospholipids in the membrane (such as the ratio of saturated to unsaturated fatty acids) can also affect permeability

Molecular Properties

  • The size, charge, and polarity of molecules affect their ability to pass through the cell membrane
  • Small, nonpolar molecules (carbon dioxide, oxygen) diffuse more readily compared to large, polar, or charged molecules (glucose, amino acids, ions)
  • Larger molecules experience more resistance when passing through the membrane due to their size and potential interactions with the hydrophobic core of the bilayer
  • Charged molecules are repelled by the hydrophobic interior of the membrane and require carrier proteins or channel proteins for transport

Protein Availability and Saturation (Facilitated Diffusion)

  • In facilitated transport, the number and availability of carrier or channel proteins determine the maximum rate of transport
  • The presence of more proteins increases the transport capacity, allowing for a higher rate of facilitated diffusion
  • Saturation of carrier proteins occurs when all the binding sites are occupied by substrate molecules, limiting the rate of transport at high substrate concentrations
  • Once saturation is reached, further increases in substrate concentration do not result in an increased rate of transport, leading to a plateau in the transport rate

Inhibitors and Competing Molecules (Facilitated Diffusion)

  • The presence of inhibitors or competing molecules can reduce the rate of facilitated transport by blocking or occupying the binding sites on carrier or channel proteins
  • Competitive inhibitors are molecules that closely resemble the substrate and compete for the same binding sites on the proteins, reducing the transport of the desired substrate
  • Non-competitive inhibitors bind to allosteric sites on the proteins, causing conformational changes that decrease the affinity for the substrate or prevent the transport process altogether
  • Example: Ouabain, a cardiac glycoside, inhibits the sodium-potassium pump (Na+/K+ ATPase) by binding to the potassium binding site, disrupting the normal transport of sodium and potassium ions across the membrane