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Introduction
1. CARS
2. Psych/soc
3. Bio/biochem
3.1 Structure and function of proteins and their constituent amino acids
3.2 Transmission of genetic information from the gene to the protein
3.3 Heredity and genetic diversity
3.4 Principles of bioenergetics and fuel molecule metabolism
3.5 Assemblies of molecules, cells, groups of cells
3.5.1 Plasma membrane
3.5.2 Membrane-bound organelles, characteristics of eukaryotic cells
3.6 Structure and physiology of prokaryotes and viruses
3.7 Processes of cell division, differentiation, and specialization
3.8 Structure and functions of nervous and endocrine systems
3.9 Structure and functions of main organ systems
4. Chem/phys
Wrapping up
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3.5.1 Plasma membrane
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3. Bio/biochem
3.5. Assemblies of molecules, cells, groups of cells

Plasma membrane

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The plasma membrane is the dynamic boundary that surrounds each cell. It helps maintain the cell’s internal environment and controls how the cell interacts with its surroundings. Its core is made of phospholipids, which form a bilayer with hydrophilic heads facing outward (toward water) and hydrophobic tails facing inward (away from water).

Embedded steroids, especially cholesterol, help regulate membrane fluidity, while small amounts of waxes can add structural stability. In the fluid mosaic model, proteins move within this lipid framework and function as channels, transporters, and surface markers.

Detailed diagram of the cell membrane structure
Detailed diagram of the cell membrane structure

Membrane dynamics

Membrane dynamics include processes such as endocytosis and exocytosis.

Endocytosis: the membrane invaginates to internalize particles or liquids in an envelope.

  • Phagocytosis- the process by which cells engulf large particles such as bacteria or cellular debris. During this process, the plasma membrane extends around the target, often aided by a coating of clathrin, to form a vesicle that internalizes the material. This vesicle then fuses with a lysosome, creating an endosome where the engulfed substance is degraded and its nutrients extracted. Once digestion is complete, the endosome can fuse with the plasma membrane again to release any residual contents into the extracellular space.
  • Pinocytosis- “cell drinking,” involves uptake of extracellular fluid and dissolved molecules into small vesicles that typically do not merge with lysosomes. A specialized form of pinocytosis, potocytosis, utilizes the protein caveolin to form distinct, receptor-rich invaginations called caveolae, which transport molecules across the cell by transcytosis or deliver them to specific organelles, such as the endoplasmic reticulum, for further processing.
  • Receptor-mediated endocytosis- a highly selective form of endocytosis in which specific cell surface receptors bind targeted molecules. These receptors, often associated with clathrin coats, trigger the formation of vesicles that internalize the bound substances. This process is critical for removing compounds like low-density lipoprotein (LDL) from the bloodstream. When receptor-mediated endocytosis fails - as seen in familial hypercholesterolemia - LDL accumulates, leading to dangerously high cholesterol levels. Moreover, some pathogens and toxins can exploit this pathway by mimicking natural ligands, thereby gaining entry into the cell.

Exocytosis: releases materials from inside the cell to the extracellular environment. Waste or secretory substances are packaged into a vesicle, and the vesicle then fuses with the inner surface of the plasma membrane. The vesicle membrane merges with the plasma membrane and opens to the outside, discharging its contents into the extracellular space. Exocytosis is responsible for the secretion of extracellular matrix proteins and the release of neurotransmitters into the synaptic cleft via synaptic vesicles.

Diagram showing different types of endocytosis in cells
Diagram showing different types of endocytosis in cells
Diagram illustrating the process of phagocytosis in cells
Diagram illustrating the process of phagocytosis in cells

Cells can also adjust their shape for chemotaxis, often directed by the cytoskeleton. The membrane allows small nonpolar molecules to diffuse directly through the bilayer, while ions generally require membrane channels or pumps.

Membrane transport

Transport across the membrane depends on thermodynamic considerations. Mixing charged ions with the hydrophobic interior of the bilayer is unfavorable, so ions typically need assistance to cross.

Osmosis allows water to diffuse freely and can generate colligative properties that affect osmotic pressure. If osmotic pressure becomes excessive, the cell risks lysis.

Passive transport (facilitated diffusion) moves substances down a concentration gradient without ATP. Active transport (such as the sodium-potassium pump) uses ATP to move solutes against their gradients, helping maintain a negative membrane potential.

Membrane receptors and cell signaling
The membrane also contains membrane receptors that initiate cell signaling pathways by producing second messengers, which change intracellular processes. Signaling types include contact signaling, chemical signaling, and electrical signaling, such as neurotransmitter release in neurons or action potentials in muscle cells.

Intercellular junctions
In tissue organization, intercellular junctions play a key role:

  • Gap junctions permit direct exchange of small molecules between adjacent cells
  • Tight junctions form barriers that prevent leakage
  • Desmosomes anchor cells together by linking their cytoskeletons
Structure of a gap junction connecting adjacent cells
Structure of a gap junction connecting adjacent cells
Diagram showing a tight junction
Diagram showing a tight junction
Diagram of desmosomal adhesion linking two adjacent cells
Diagram of desmosomal adhesion linking two adjacent cells

Plasma membrane structure

  • Phospholipid bilayer: hydrophilic heads outward, hydrophobic tails inward
  • Cholesterol regulates fluidity; waxes add stability
  • Fluid mosaic model: proteins move within lipid bilayer, act as channels, transporters, markers

Membrane dynamics

  • Endocytosis: membrane engulfs material into vesicles
    • Phagocytosis: large particles, clathrin-coated, fuses with lysosome (endosome)
    • Pinocytosis: uptake of fluid, caveolin/caveolae in potocytosis, transcytosis
    • Receptor-mediated: selective, clathrin-coated, removes LDL, can be hijacked by pathogens
  • Exocytosis: vesicles fuse with membrane to release contents (e.g., neurotransmitters, proteins)
  • Chemotaxis: membrane shape changes, cytoskeleton-driven
  • Small nonpolar molecules diffuse directly; ions need channels/pumps

Membrane transport

  • Osmosis: water diffusion, affects osmotic pressure, risk of lysis if excessive
  • Passive transport: down gradient, no ATP (facilitated diffusion)
  • Active transport: against gradient, uses ATP (e.g., sodium-potassium pump), maintains membrane potential

Membrane receptors and cell signaling

  • Membrane receptors trigger cell signaling via second messengers
  • Types: contact signaling, chemical signaling, electrical signaling (e.g., neurotransmitter release, action potentials)

Intercellular junctions

  • Gap junctions: direct exchange of small molecules between cells
  • Tight junctions: form barriers, prevent leakage
  • Desmosomes: anchor cells by linking cytoskeletons

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Plasma membrane

The plasma membrane is the dynamic boundary that surrounds each cell. It helps maintain the cell’s internal environment and controls how the cell interacts with its surroundings. Its core is made of phospholipids, which form a bilayer with hydrophilic heads facing outward (toward water) and hydrophobic tails facing inward (away from water).

Embedded steroids, especially cholesterol, help regulate membrane fluidity, while small amounts of waxes can add structural stability. In the fluid mosaic model, proteins move within this lipid framework and function as channels, transporters, and surface markers.

Membrane dynamics

Membrane dynamics include processes such as endocytosis and exocytosis.

Endocytosis: the membrane invaginates to internalize particles or liquids in an envelope.

  • Phagocytosis- the process by which cells engulf large particles such as bacteria or cellular debris. During this process, the plasma membrane extends around the target, often aided by a coating of clathrin, to form a vesicle that internalizes the material. This vesicle then fuses with a lysosome, creating an endosome where the engulfed substance is degraded and its nutrients extracted. Once digestion is complete, the endosome can fuse with the plasma membrane again to release any residual contents into the extracellular space.
  • Pinocytosis- “cell drinking,” involves uptake of extracellular fluid and dissolved molecules into small vesicles that typically do not merge with lysosomes. A specialized form of pinocytosis, potocytosis, utilizes the protein caveolin to form distinct, receptor-rich invaginations called caveolae, which transport molecules across the cell by transcytosis or deliver them to specific organelles, such as the endoplasmic reticulum, for further processing.
  • Receptor-mediated endocytosis- a highly selective form of endocytosis in which specific cell surface receptors bind targeted molecules. These receptors, often associated with clathrin coats, trigger the formation of vesicles that internalize the bound substances. This process is critical for removing compounds like low-density lipoprotein (LDL) from the bloodstream. When receptor-mediated endocytosis fails - as seen in familial hypercholesterolemia - LDL accumulates, leading to dangerously high cholesterol levels. Moreover, some pathogens and toxins can exploit this pathway by mimicking natural ligands, thereby gaining entry into the cell.

Exocytosis: releases materials from inside the cell to the extracellular environment. Waste or secretory substances are packaged into a vesicle, and the vesicle then fuses with the inner surface of the plasma membrane. The vesicle membrane merges with the plasma membrane and opens to the outside, discharging its contents into the extracellular space. Exocytosis is responsible for the secretion of extracellular matrix proteins and the release of neurotransmitters into the synaptic cleft via synaptic vesicles.

Cells can also adjust their shape for chemotaxis, often directed by the cytoskeleton. The membrane allows small nonpolar molecules to diffuse directly through the bilayer, while ions generally require membrane channels or pumps.

Membrane transport

Transport across the membrane depends on thermodynamic considerations. Mixing charged ions with the hydrophobic interior of the bilayer is unfavorable, so ions typically need assistance to cross.

Osmosis allows water to diffuse freely and can generate colligative properties that affect osmotic pressure. If osmotic pressure becomes excessive, the cell risks lysis.

Passive transport (facilitated diffusion) moves substances down a concentration gradient without ATP. Active transport (such as the sodium-potassium pump) uses ATP to move solutes against their gradients, helping maintain a negative membrane potential.

Membrane receptors and cell signaling
The membrane also contains membrane receptors that initiate cell signaling pathways by producing second messengers, which change intracellular processes. Signaling types include contact signaling, chemical signaling, and electrical signaling, such as neurotransmitter release in neurons or action potentials in muscle cells.

Intercellular junctions
In tissue organization, intercellular junctions play a key role:

  • Gap junctions permit direct exchange of small molecules between adjacent cells
  • Tight junctions form barriers that prevent leakage
  • Desmosomes anchor cells together by linking their cytoskeletons
Key points

Plasma membrane structure

  • Phospholipid bilayer: hydrophilic heads outward, hydrophobic tails inward
  • Cholesterol regulates fluidity; waxes add stability
  • Fluid mosaic model: proteins move within lipid bilayer, act as channels, transporters, markers

Membrane dynamics

  • Endocytosis: membrane engulfs material into vesicles
    • Phagocytosis: large particles, clathrin-coated, fuses with lysosome (endosome)
    • Pinocytosis: uptake of fluid, caveolin/caveolae in potocytosis, transcytosis
    • Receptor-mediated: selective, clathrin-coated, removes LDL, can be hijacked by pathogens
  • Exocytosis: vesicles fuse with membrane to release contents (e.g., neurotransmitters, proteins)
  • Chemotaxis: membrane shape changes, cytoskeleton-driven
  • Small nonpolar molecules diffuse directly; ions need channels/pumps

Membrane transport

  • Osmosis: water diffusion, affects osmotic pressure, risk of lysis if excessive
  • Passive transport: down gradient, no ATP (facilitated diffusion)
  • Active transport: against gradient, uses ATP (e.g., sodium-potassium pump), maintains membrane potential

Membrane receptors and cell signaling

  • Membrane receptors trigger cell signaling via second messengers
  • Types: contact signaling, chemical signaling, electrical signaling (e.g., neurotransmitter release, action potentials)

Intercellular junctions

  • Gap junctions: direct exchange of small molecules between cells
  • Tight junctions: form barriers, prevent leakage
  • Desmosomes: anchor cells by linking cytoskeletons