ch.8 Flashcards

(47 cards)

1
Q

Biological Membrane Structure and Function

A

Structure: Composed of phospholipid bilayer, proteins, and cholesterol.
Functions:
Acts as a barrier, regulating entry and exit of substances.
Facilitates communication between cells.
Provides structural support and shape to cells.
Plays a role in metabolic reactions and signal transduction.

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2
Q

Fluid Mosaic Model of Plasma Membrane

A

Description: The membrane is fluid with proteins embedded in or attached to a flexible lipid bilayer.

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3
Q

Key Experiment fluid mosaic model

A

Mouse and human cells were fused, and over time, proteins intermixed. This showed lateral movement of proteins and supported the model of fluidity in membranes.

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4
Q

Membrane Fluidity and Permeability

A

Fluidity: Refers to the ability of membrane lipids and proteins to move laterally within the bilayer.
Relation to Permeability: Higher fluidity generally increases permeability, allowing more substances to pass through

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5
Q

Factors Affecting Membrane Fluidity

A

temperature, saturation of fatty acids, fatty acid length, cholesterol

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6
Q

Temperature on membrane fluidity

A

Increase: Increases fluidity as lipid molecules move faster.
Decrease: Reduces fluidity as molecules pack more tightly.

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7
Q

Saturation of Fatty Acids and membrane fluidity

A

Saturated Fats: Decrease fluidity as they pack closely together.
Unsaturated Fats: Increase fluidity due to kinks in their structure, preventing tight packing.

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8
Q

Fatty Acid Length and membrane fluidity

A

Long Chains: Decrease fluidity due to more interactions.
Short Chains: Increase fluidity as there are fewer interactions between chains

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9
Q

Cholesterol and membrane fluidity

A

Fluidity Buffer: Stabilizes fluidity by preventing membrane from becoming too fluid at high temperatures and too rigid at low temperatures.

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10
Q

Adaptations in Membrane Composition

A

Homeoviscous Adaptation: Ability of some organisms to adjust membrane lipid composition in response to environmental changes, maintaining optimal fluidity.

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11
Q

Classes of Membrane Proteins

A

Integral Proteins: Span the membrane; e.g., transport proteins.
Peripheral Proteins: Attach to surface of membrane; e.g., enzymes.

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12
Q

Transmembrane Proteins

A

Structure: Amphipathic with hydrophobic regions within the bilayer and hydrophilic regions exposed to water on both sides.
Function: Facilitate specific transport, cell signaling, and structural support.

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13
Q

Asymmetry in Membrane Faces

A

Distribution: Cytoplasmic (inner) and extracellular (outer) leaflets have distinct lipid and protein compositions, which are essential for specific cellular functions.

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14
Q

Selective Permeability of Membranes

A

Definition: Allows selective passage of certain substances.
Importance: Maintains cell homeostasis.
Roles of Components:
Lipids: Provide a hydrophobic barrier.
Proteins: Act as channels, carriers, and receptors to facilitate movement.

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15
Q

Six Functional Classes of Membrane Proteins

A

Transport: Channels and carriers for substances.
Enzymatic Activity: Catalyze reactions.
Signal Transduction: Receptors for signals.
Cell Recognition: Glycoproteins identify cells.
Intercellular Joining: Junctions between cells.
Attachment: Anchors for cytoskeleton or ECM.

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16
Q

Cell Junctions in Eukaryotes

A

Types:
Tight Junctions: Prevent leakage between cells.
Desmosomes: Provide mechanical stability.
Gap Junctions: Allow direct communication.

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17
Q

Plant vs. Animal Cells

A

Plant Cells: Plasmodesmata link cells.
Animal Cells: Use gap junctions for communication.

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18
Q

Membrane Synthesis

A

Process: Built in the ER and Golgi apparatus.
Glycoproteins and Glycolipids: Carbohydrates are added to the extracellular face in the Golgi, and appear on the outer side when vesicles fuse with the membrane.

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19
Q

Diffusion and Concentration Gradient

A

Definition: Passive movement of molecules from high to low concentration.
Driving Force: Concentration gradient; occurs spontaneously until equilibrium.

20
Q

Net Diffusion and Dynamic Equilibrium

A

Net Diffusion: Movement of molecules with a net direction until equilibrium.
Dynamic Equilibrium: Molecule movement continues with no net change in concentration.

21
Q

Factors Influencing Diffusion Rate

A

Molecule Size: Smaller molecules diffuse faster.
Temperature: Higher temperature increases rate.
Concentration Gradient: Larger gradients increase rate.

22
Q

Simple vs. Facilitated Diffusion

A

Simple Diffusion: Passive movement of small, nonpolar molecules.
Facilitated Diffusion: Uses channels/carriers for larger or polar molecules.

23
Q

Transporters in Membranes

A

Function: Proteins that assist in moving substances across membranes.
Mechanisms:
Channels: Provide a pathway for ions.
Carriers: Bind substances and undergo shape changes.

24
Q

Gated Channels

A

Description: Open in response to stimuli.
Types:
Voltage-Gated: Respond to electrical signals.
Ligand-Gated: Open with specific molecule binding.
Function: Control ion flow and cell signaling.

25
Osmosis and Osmotic Gradient
Definition: Water diffusion across a membrane. Driving Force: Osmotic gradient, moving water to balance solute concentrations.
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Osmotic Pressure:
Pressure needed to stop water flow.
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Osmolarity:
Total solute concentration.
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Tonicity:
Effect of a solution on cell volume (isotonic, hypotonic, hypertonic).
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Predicting Water Movement
Animal Cells: Swell in hypotonic, shrink in hypertonic Plant Cells: Turgor pressure supports structure; plasmolysis in hypertonic.
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Active Transport
Process: Moves substances against gradient using energy. Difference from Facilitated Diffusion: Active transport requires ATP; facilitated diffusion does not.
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Pump Mechanisms
Example: Na+/K+ pump moves ions against gradient, maintaining cellular ion balance. Electrogenic Pumps: Create voltage difference; Na+/K+ in animals, proton pumps in plants.
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Electrochemical Gradients and Membrane Potential
Gradient: Combination of electrical and chemical potential across a membrane. Membrane Potential: Voltage difference maintained by ion distribution.
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Secondary Active Transport
Process: Uses energy from gradients created by primary pumps. Example: H+/sucrose symporter in plants; Na+/glucose in animals.
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Types of Bulk Transport
exocytosis, endocytosis
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Exocytosis:
Exocytosis is the process by which cells move large molecules or particles, like proteins or waste, from the inside of the cell to the outside.
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Endocytosis
Endocytosis is the process by which cells take in large particles, such as nutrients or debris, by engulfing them in a section of the plasma membrane that pinches off into the cell.
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Isotonic Solution
Definition: The concentration of solutes outside the cell is equal to the concentration inside the cell. Animal Cells: No net movement of water; cell volume remains stable. Plant Cells: Cells maintain shape but are not as firm as in a hypotonic environment since turgor pressure is minimal. Example: Physiological saline (0.9% NaCl) is isotonic to human cells, so cells retain their normal shape and function.
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Hypotonic Solution
Definition: The concentration of solutes is lower outside the cell than inside. Animal Cells: Water enters the cell, causing it to swell. Cells may burst (lyse) if too much water enters. Plant Cells: Water enters, increasing turgor pressure, which supports the cell wall and gives structure to the plant. Cells become turgid (firm). Example: Distilled water is hypotonic to cells; it causes animal cells to swell and plant cells to become firm.
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Hypertonic Solution
Definition: The concentration of solutes is higher outside the cell than inside. Animal Cells: Water leaves the cell, causing it to shrink (crenate). Plant Cells: Water leaves the cell, and the cell membrane pulls away from the cell wall (plasmolysis), leading to wilting. Example: A solution with high salt concentration (like seawater) is hypertonic to human cells, causing them to shrink as water exits.
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Mechanism for exocytosis
Vesicle Formation: Molecules that need to be exported are packaged into membrane-bound vesicles, usually in the Golgi apparatus. Vesicle Transport: The vesicle moves toward the plasma membrane, typically along cytoskeletal structures (microtubules). Vesicle Fusion: The vesicle membrane fuses with the plasma membrane. This fusion requires energy (usually from ATP) and specific proteins called SNAREs to facilitate the merging of the two membranes. Release of Contents: Once the vesicle membrane has fused, its contents are released into the extracellular environment. Membrane Recycling: The vesicle membrane becomes part of the plasma membrane, helping to maintain membrane surface area.
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Functions of exocytosis
Secretion of Proteins and Hormones: Many cells use exocytosis to release proteins (e.g., antibodies by immune cells) and hormones (e.g., insulin from pancreatic cells). Waste Removal: Cells expel waste products that cannot be broken down internally. Membrane Expansion: Adds phospholipids and proteins to the plasma membrane, aiding in cell growth and repair.
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Types of exocytosis
Constitutive Exocytosis: A continuous process where vesicles fuse with the membrane without regulation, typically for membrane repair and general secretion. Regulated Exocytosis: Triggered by specific signals, such as a neural impulse or hormone binding, as seen in neurotransmitter release at synapses.
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Mechanism of endocytosis
Membrane Invagination: The cell membrane folds inward to form a pocket around the targeted material. Vesicle Formation: The pocket deepens and eventually pinches off, forming a vesicle within the cell, enclosing the material from the extracellular environment. Internalization and Transport: The vesicle can then be transported to different cellular compartments for processing, degradation, or use.
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Types of Endocytosis
1. phagocytosis 2. pinocytosis 3. receptor-mediated endocytosis
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Phagocytosis ("Cell Eating"):
Description: Large particles like bacteria, dead cells, or food particles are engulfed by the cell. Mechanism: The plasma membrane extends around the particle, forming a phagosome that enters the cell. The phagosome then typically fuses with a lysosome, where digestive enzymes break down the particle. Example: White blood cells (macrophages) use phagocytosis to engulf pathogens and debris as part of the immune response.
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Pinocytosis ("Cell Drinking"):
Description: The cell takes in extracellular fluid and dissolved solutes in small vesicles. Mechanism: The cell membrane forms small, fluid-filled vesicles that contain molecules from outside the cell. Example: Common in cells of the digestive system and kidney tubules, where fluids and solutes need to be absorbed continuously.
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Receptor-Mediated Endocytosis:
Description: Allows the cell to take in specific molecules with the help of cell surface receptors that recognize and bind to particular ligands (molecules like hormones, vitamins, or lipoproteins). Mechanism: Binding: Target molecules in the extracellular fluid bind to specific receptors on the cell surface. Vesicle Formation: Once bound, the receptor-ligand complexes cluster together, and a vesicle forms around them. Internalization: The vesicle enters the cell and is processed in endosomes, where ligands may be released and transported to other parts of the cell or delivered to lysosomes for degradation. Example: Uptake of cholesterol by cells using low-density lipoprotein (LDL) receptors.