1. Chapter 5
Membrane Dynamics

2. About this Chapter Cell membrane structures and functions
Membranes form fluid body compartments
Membranes as barriers and gatekeepers
How products move across membranes
Distribution of water and solutes in cells & the body
Chemical and electrical imbalances
Membrane permeability and changes

3. Membranes: two meanings
Membranous tissues:
Example: pericardial membrane
Epithelial tissues: one to many cells thick
Cell Membranes (plasmalemma) enclose cells
Figure 5-1: Membranes in the body

4. Cell Membranes: Overview
Cell structure & support
Barrier isolates cell (impermeable)
Chemically
Physically
Regulates exchange (semipermeable)
Cell communication

5. Cell Membranes: Overview
Figure 5-2: The fluid mosaic model of the membrane

6. Membrane Structure Phospholipid bilayer and cholesterol
Membrane proteins
Peripheral (associated)
Integral

7. Structural Membrane Proteins: Membrane-Spanning
Structure
Cell polarity
Phosphorylation
Extracellular matrix

8. Structural Membrane Proteins: Membrane-Spanning
Figure 5-4: The cytoskeleton is anchored to the cell membrane

9. Structural Membrane Proteins: Membrane-Spanning
Figure 5-5: Membrane-spanning proteins

10. Membrane Proteins that Bind Molecules
Membrane associated enzymes
External reactions
Internal reactions
Receptors bind specific ligand
Example: Hormones
Cell recognition molecules
Figure 5-6: Cell membrane receptor

11. Transporter Proteins: Move Products Through Membrane
Channel proteins
Open
Gated
Carrier proteins
Bind to substrate
Slower transport

12. Transporter Proteins: Move Products Through Membrane
Figure 5-7: Transport proteins of the cell membrane

13. Transporter Proteins: Move Products Through Membrane
Figure 5-9: Gating of channel proteins

14. Membrane Carbohydrates: Form External Glycocalyx
The term was initially applied to the polysaccharide matrix excreted by epithelial cells forming a coating on the surface of epithelial tissue
Includes Glycoproteins and Glycolipids
Figure 5-11: Map of cell membrane structure

15. The Glycocalyx
glycocalyx — carbohydrate-rich peripheral zone of the external surface coating of the membrane in most eukaryotic cells.
Description
The outer surface of cells is covered with lipopolysaccharide "hairs" consisting of proteoglycans, glycoproteins and glycolipids, which are called “glycocalyx” Carbohydrate components of the glycocalyx include both compounds covalently bound to proteins or, to a lesser extent, to lipids on the cell surface, and additional glycoproteins and polysaccharides which are non-covalently attached to them. Some of the adsorbed macromolecules are components of the extracellular matrix, which makes it difficult to distinguish between such matrices and the glycocalyx with the cell membrane. Glycocalyx is considered as a protective layer on the vessel wall against pathogenic effects, a network barrier to the movement of molecules. It is assumed that the endothelial glycocalyx has a definite ultrastructure and may be connected with the cytoskeleton to serve as a mechanochemical transducer of blood flow effects (shear stress) into other processes of cell signaling.

18. Functions of the Glycocalyx
Protection: Cushions the plasma membrane and protects it from chemical injury
Immunity to infection: Enables the immune system to recognize and selectively attack foreign organisms
Defense against cancer: Changes in the glycocalyx of cancerous cells enable the immune system to recognize and destroy them
Transplant compatibility: Forms the basis for compatibility of blood transfusions, tissue grafts, and organ transplants
Cell adhesion: Binds cells together so that tissues do not fall apart
Inflammation regulation: Glycocalyx coating on endothelial walls in blood vessels prevents leukocytes from rolling/binding in healthy states[4]
Fertilization: Enables sperm to recognize and bind to eggs
Embryonic development: Guides embryonic cells to their destinations in the body

19. Membrane Proteins and Functions Reviewed
Figure 5-12: Map of membrane proteins

20. Body Fluid Compartments
Intracellular (ICF)
Extracellular (ECF)
Interstitial
Plasma
Figure 5-13: Body fluid compartments

21. Overview of Movement Across Membranes
Energy requirements
Physical requirements
Figure 5-14: Map of the ways molecules move across cell membranes

22. Diffusion: Passive & down a concentration gradient
Stops at equilibrium
Rate factors: membrane, temperature, distance, & size
Figure 5-16: Fick’s law of diffusion

23. Carrier Mediated Transport: Can be Passive or Active
Uniport
Cotransport
Symport
Antiport
Figure 5-17: Types of carrier-mediated transport

24. Facilitated Diffusion
Uses transport proteins
Passive Diffusion to Equilibrium
Figure 5- 21: Diffusion stops at equilibrium (panoramic lower left 66%)

25. Facilitated Diffusion
Figure 5-22: Diffusion of glucose into cells

26. Primary Active Transport: Pumps Products
Uses ATP to move products
Up a concentration gradient
Figure 5-23: The Na+ - K+ -ATPase

27. Primary Active Transport: Pumps Products
Figure 5-24: Mechanism of the Na+ - K+ -ATPase (75%)

28. Secondary Active Transport: Uses Kinetic Energy of [ion]
Cotransports
[Ion ] restored
using ATP
Figure 5-25: Sodium-glucose symporter

29. Energy Transfer: Review
Cell metabolism (Chapter 4)
Membrane transport (Chapter 5)
Figure 5-26: Energy transfer in living cells

30. Endocytosis Pathways
Clathrin-mediated endocytosis is mediated by small (approx. 100 nm in diameter) vesicles that have a morphologically characteristic coat made up of a complex of proteins that are mainly associated with the cytosolic protein clathrin. Clathrin-coated vesicles (CCVs) are found in virtually all cells and form domains of the plasma membrane termed clathrin-coated pits. Coated pits can concentrate large extracellular molecules that have different receptors responsible for the receptor-mediated endocytosis of ligands, e.g. low density lipoprotein, transferrin, growth factors, antibodies and many others.
Caveolae are the most common reported non-clathrin-coated plasma membrane buds, which exist on the surface of many, but not all cell types. They consist of the cholesterol-binding protein caveolin (Vip21) with a bilayer enriched in cholesterol and glycolipids. Caveolae are small (approx. 50 nm in diameter) flask-shape pits in the membrane that resemble the shape of a cave (hence the name caveolae). They can constitute up to a third of the plasma membrane area of the cells of some tissues, being especially abundant in smooth muscle, type I pneumocytes, fibroblasts, adipocytes, and endothelial cells. Uptake of extracellular molecules is also believed to be specifically mediated via receptors in caveolae.
Macropinocytosis, which usually occurs from highly ruffled regions of the plasma membrane, is the invagination of the cell membrane to form a pocket, which then pinches off into the cell to form a vesicle (0.5–5 µm in diameter) filled with a large volume of extracellular fluid and molecules within it (equivalent to ~100 CCVs). The filling of the pocket occurs in a non-specific manner. The vesicle then travels into the cytosol and fuses with other vesicles such as endosomes and lysosomes.
Phagocytosis is the process by which cells bind and internalize particulate matter larger than around 0.75 µm in diameter, such as small-sized dust particles, cell debris, micro-organisms and even apoptotic cells, which only occurs in specialized cells. These processes involve the uptake of larger membrane areas than clathrin-mediated endocytosis and caveolae pathway.

31. Vesicles in Membrane Transport
Transcytosis: Moves some molecules and large proteins and particles via endocytosis and exocytosis across cell membrane
Phagosome: The vesicle formed via internalization, in phagocytic cells. Binds and internalizes particles > 0.75 microns
Phagocytes: An Actin-mediated process. Examples, immune cells
Clatherin-Mediated Endocytosis
Caveolae: Non-Clatherin coated but have caveolin

32. Endocytosis and Exocytosis: VacuoleTransport
Pinocytosis: non-selective
Receptor mediated: specific substrate

33. Endocytosis and Exocytosis: VacuoleTransport
Figure 5-28: Receptor-mediated endocytosis and exocytosis

34. CAVEOLAE

35. CAVEOLAE

36. Transcytosis
Figure 5-31: Transcytosis across the capillary endothelium

39. Transepithelial Transport
Cross two membranes
Apical
Basolateral
Absorption
Secretion

42. Transepithelial Transport
Figure 5-30: Transepithelial transport of glucose

43. Distribution of Water and Solutes in the Body Compartments
About 60% of body weight is water
67% water -intracellular
33% water -extracellular
8% plasma
25% interstitial
% varies slightly with sex and age
Figure 5-32: Distribution of volume in the body fluid compartments

44. Molarity vs Molality
Molarity is defined as the number of moles of solute per liter of solution.  This means that if you have a 1 M solution of some compound, evaporating one liter will cause one mole of the solute to precipitate.
Molality is defined as the number of moles of solute per kilogram of solvent.  To make a 1 m solution, you'd take one mole of a substance and add it to 1 Kg of solvent.  As a result, the final volume of a 1 m solution will be somewhat more than 1 L if the solvent is Water.

45. Molality
Molalities are more convenient than molarities in experiments that involve significant temperature changes. Because the volume of a solution increases when its temperature increases, heating makes the solutions molarity go down- but the molality, which is based on masses rather than volumes, remains unchanged.

46. Osmolarity vs Osmolality
Osmolarity is distinct from molarity because it measures moles of solute particles rather than moles of solute. The distinction arises because some compounds can dissociate in solution, whereas others cannot
Plasma osmolality is affected by changes in water content. In comparison, the plasma osmolarity is slightly less than osmolality, because the total plasma weight (the divisor used for osmolality) excludes the weight of any solutes, while the total plasma volume (used for osmolarity) includes solute content. Otherwise, one liter of plasma would be equivalent to one kilogram of plasma, and plasma osmolarity and plasma osmolality would be equal. However, at low concentrations, the weight of the solute is negligible compared to the weight of the solvent, and osmolarity and osmolality are very similar.

47. Osmosis and Osmotic Equilibrium
Water freely crosses membranes
Osmotic pressure (mmHg)
Osmolarity
Osmolality
Comparing two solutions
Isosmotic
Hyperosmotic
Hyposmotic
Figure 5-34: Osmosis and osmotic pressure

51. Tonicity: How a Cell Reacts in a Solution
Penetrating solute
Non-penetrating solute
Isotonic
Hypertonic
Hypotonic
Figure 5-35a, b: Tonicity depends on the relative concentrations of nonpenetrating solutes

52. Tonicity: How a Cell Reacts in a Solution
Figure 5-35c, d: Tonicity depends on the relative concentrations of nonpenetrating solutes

53. Electrical Disequilibrium
Separation of charged ions
Membrane insulates
Potential
Conduction of signal
Electrochemical gradient

54. Electrical Disequilibrium
Figure 5-36a, b: Separation of electrical charge

55. Membrane Potentials: Change with Permeability
Resting
Equilibrium
Channel opening
Voltage gated
ATP gated (leak)

56. Membrane Potentials: Change with Permeability
Figure 5-38a, b: Potassium equilibrium potential

57. Membrane Potentials: Change with Permeability
Figure 5-38c: Potassium equilibrium potential

58. Membrane Potentials: Change with Permeability
Figure 5-39: Sodium equilibrium potential

60. Figure 5-42a: Insulin secretion and membrane transport processes
Summary
Figure 5-42a: Insulin secretion and membrane transport processes

61. Figure 5-42b: Insulin secretion and membrane transport processes
Summary
Figure 5-42b: Insulin secretion and membrane transport processes