Chapter 5
CHAPTER 5: PLASMA MEMBRANES, TRANSPORT, AND ENZYMES
Introduction
- Grand Central Station serves as an analogy for cell function; organized movement reflects cellular processes across the plasma membrane.
- Plasma Membrane (Cell Membrane): Defines the cell's borders, maintaining functionality.
- Selective Permeability: Allows certain materials to enter or exit freely, while others require specific transport mechanisms.
5.1 | Components and Structure
Objectives
- Understand the Fluid Mosaic Model of the cell membrane.
- Describe the functions of phospholipids, proteins, and carbohydrates in membranes.
- Discuss membrane fluidity and its implications.
Structure of the Plasma Membrane
- Functionality: Defines boundaries, controls substance movement, and facilitates communication between cells.
- Flexibility: Important for the shape changes in cells, such as red and white blood cells.
- Recognition Markers: The surface of the membrane has markers necessary for cell recognition, crucial in immune response and tissue formation.
Fluid Mosaic Model
- Description of the plasma membrane as a combination of components:
- Phospholipids
- Cholesterol
- Proteins
- Glycolipids
- Membrane Thickness: Ranges from 5 to 10 nm.
- Carbohydrates (Glycoproteins and Glycolipids): Extend from the surface, playing roles in recognition and signaling.
Components of the Plasma Membrane
Phospholipids: Composed of a glycerol, two fatty acids, and a phosphate group.
- Amphipathic Nature: Hydrophilic heads and hydrophobic tails contribute to bilayer formation in aqueous environments.
- Arrangement: In water, they form a lipid bilayer with hydrophilic heads outward and hydrophobic tails inward.
Proteins: Integral (spanning the membrane) and peripheral (on the membrane's surface).
- Integral Proteins: Can be transmembrane (cross the membrane completely) or associated with one layer only.
- Peripheral Proteins: Attached to the exterior/interior surfaces and involved in various cellular functions including enzymatic activity and cytoskeletal attachment.
Cholesterol: Modulates membrane fluidity; maintains structure at varying temperatures by preventing phase transitions in phospholipids.
Carbohydrates (Glycocalyx): Function in cellular recognition and attraction of water, important for cell-signaling and identification.
- Compositions of glycocalyx help immune cells distinguish between self and non-self cells.
Membrane Fluidity
- Fluidity Factors: Temperature, lipid composition, and the presence of cholesterol impact the fluidity of membranes.
- Proteins and lipids can move within the bilayer, allowing the membrane to self-seal and maintain integrity.
5.2 | Passive Transport
Objectives
- Explain the mechanisms of passive transport.
- Understand osmosis and diffusion processes.
- Define tonicity relative to cell movement.
Passive Transport Overview
- Definition: Natural movement of materials across cell membranes without energy use, moving down the concentration gradient.
- Diffusion: Movement from high to low concentration until equilibrium is achieved.
- Osmosis: Water movement through semipermeable membranes driven by solute concentration gradients.
Selective Permeability
- Plasma membranes facilitate specific substances' passage depending on molecular polarity, charge, and size.
- Nonpolar and Lipid-Soluble Molecules: Easily diffuse through the bilayer.
- Polar Molecules and Ions: Require specific membrane proteins to aid transport.
Factors Affecting Diffusion Rates
- Concentration Gradient: Greater differences drive faster diffusion.
- Molecule Mass: Lighter molecules diffuse more quickly.
- Temperature: Higher temperatures increase diffusion rates.
- Solubility: Nonpolar substances pass through membranes faster.
- Surface Area/Thickness of Membrane: Larger surface areas promote faster diffusion; thicker membranes slow down the process.
- Distance Travelled: Greater distances reduce diffusion rates.
Facilitated Diffusion
- Uses transport proteins (channels or carriers) to assist polar molecules and ions across the membrane.
- Aquaporins: Specific channel proteins facilitating rapid water movement.
- Carrier proteins undergo conformational changes when binding substances to propel them across the membrane.
5.3 | Active Transport
Objectives
- Understand how electrochemical gradients affect ions.
- Distinguish between primary and secondary active transport mechanisms.
Overview of Active Transport
- Definition: Movement against concentration gradients requiring energy, often from ATP.
- Active Transport Mechanisms: Pumps that maintain ion concentration by moving substances against their gradient.
Primary Active Transport
- Example: Sodium-Potassium Pump (Na+-K+ ATPase)
- Pumps sodium ions out of the cell and potassium ions in (3 Na+ for every 2 K+), both against their concentration gradients, powered by ATP.
Secondary Active Transport
- Utilizes the energy generated from primary active transport to move other substances.
- Relies on the established concentration gradients created by primary active transport to drive the movement of new substances.
5.4 | Bulk Transport
Objectives
- Describe endocytosis (including phagocytosis, pinocytosis, and receptor-mediated endocytosis).
- Understand exocytosis processes.
Endocytosis
- Process for large material transport into cells via vesicle formation.
- Types:
- Phagocytosis: “Cell eating”; engulfing of large particles or cells (e.g., macrophages targeting pathogens).
- Pinocytosis: “Cell drinking”; uptake of fluids and smaller molecules.
- Receptor-Mediated Endocytosis: Specific uptake of target molecules after binding to membrane receptors.
Exocytosis
- Process where materials are expelled from the cell by fusing vesicles with the plasma membrane.
- Key processes include neurotransmitter release and protein secretion.
5.5 | Enzymes
Objectives
- Describe exergonic and endergonic reactions.
- Explain enzyme efficiencies as molecular catalysts.
- Discuss enzyme regulation by various factors.
Enzyme Functionality
- Catalysts: Enzymes speed up chemical reactions by lowering activation energies.
- Enzymatic Action: Bind to substrates forming complexes that facilitate product formation.
- Substrate Binding: Occurs at the active site, specific to substrates which ensure reaction specificity.
Activation Energy
- Energy required to initiate a reaction; enzymes reduce this energy barrier.
- Distinction between exergonic (energy-releasing) and endergonic (energy-absorbing) reactions.
Enzyme Regulation
- Enzymes can be inhibited or activated, impacting metabolic pathways:
- Competitive Inhibition: Inhibitors compete with the substrate for the active site.
- Noncompetitive Inhibition: Inhibitors bind elsewhere, altering active site shape.
- Allosteric Regulation: Modulators change enzyme shape to increase or decrease substrate binding affinity.
Enzyme Compartmentalization
- Eukaryotic cells compartmentalize enzymes into organelles, enhancing reaction efficiency.
Feedback Inhibition in Metabolic Pathways
- End products of pathways can inhibit upstream reactions, regulating enzymatic activity based on necessity.
Key Terms
- Activation Energy: Energy necessary for reactions.
- Active Site: Specific enzymatic binding location.
- Active Transport: Energy-requiring material movement.
- Adenosine Triphosphate (ATP): Primary energy currency in cells.
- Endocytosis: Active transport for moving substances into a cell.
- Exocytosis: Active process for expelling materials from a cell.
- Facilitated Diffusion: Passage through membrane via proteins