2. The Plasma Membrane Honors Biology Chapter 6

3. History of the Plasma Membrane  1665: Robert Hooke  1895: Charles Overton - composed of lipids  1900-1920’s: must be a phospholipid  1925: E. Gorter and G. Grendel - phospholipid bilayer  1935: J.R. Danielli and H. Davson – proteins also part, proposed the Sandwich Model  1950’s: J.D. Robertson – proposed the Unit Membrane Model  1972: S.J. Singer and G.L. Nicolson – proposed Fluid Mosaic Model

4. Plasma Membrane is made of Phospholipids  Gorter + Grendel –Red Blood Cells analyzed –Enough for Phospholipid bilayer –Polar heads face out and Nonpolar tails face in –Does not explain why some nonlipids are permeable

5. Plasma Membrane Models Sandwich Model (Danielli + Davson) 2 layers of globular proteins with phospholipid inside to make a layer and then join 2 layers together to make a channel for molecules to pass Unit Membrane Model (Robertson) Outer layer of protein with phospholipid bilayer inside, believed all cells same composition, does not explain how some molecules pass through or the use of proteins with nonpolar parts, used transmission electron microscopy Fluid Mosaic Model (Singer + Nicolson) Phospholipid bilayer with proteins partially or fully imbedded, electron micrographs of freeze- fractured membrane

6. Which membrane model is correct? 1) Rapidly freeze specimen 2) Use special knife to cut membrane in half 3) Apply a carbon + platinum coating to the surface 4) Use scanning electron microscope to see the surface According to the electron micrograph which membrane model is correct? Why? Fluid-Mosaic Model

7.  Fluid – the plasma membrane is the consistency of olive oil at body temperature, due to unsaturated phospholipids. (cells differ in the amount of unsaturated to saturated fatty acid tails)  Most of the lipids and some proteins drift laterally on either side. Phospholipids do not switch from one layer to the next.  Cholesterol affects fluidity: at body temperature it lessens fluidity by restraining the movement of phospholipids, at colder temperatures it adds fluidity by not allowing phospholipids to pack close together.  Mosaic – membrane proteins form a collage that differs on either side of the membrane and from cell to cell (greater than 50 types of proteins), proteins span the membrane with hydrophilic portions facing out and hydrophobic portions facing in. Provides the functions of the membrane

8. Structure of the Plasma Membrane

9.  Phospholipid bilayer  Phospholipid –Hydrophilic head –Hydrophobic tails  Cholesterol  Proteins –Transmembrane/ Intrinsic/Integral –Peripheral/Extrinsic  Cytoskeletal filaments  Carbohydrate chain  Glycoproteins  Glycolipids

10. Label the Blank Diagram of the Plasma Membrane  Phospholipid bilayer  Phospholipid –Hydrophilic head –Hydrophobic tails  Cholesterol  Proteins –Transmembrane/ Intrinsic/Integral –Peripheral/Extrinsic  Cytoskeletal filaments  Carbohydrate chain  Glycoproteins  Glycolipids

11. Proteins of the Plasma Membrane Provide 6 Membrane Functions: 1) Transport Proteins 2) Receptor Proteins 3) Enzymatic Proteins 4) Cell Recognition Proteins 5) Attachment Proteins 6) Intercellular Junction Proteins Proteins

12. 1) Transport Proteins Channel Proteins – channel for lipid insoluble molecules and ions to pass freely through Carrier Proteins – bind to a substance and carry it across membrane, change shape in process

13. 2) Receptor Proteins – Bind to chemical messengers (Ex. hormones) which sends a message into the cell causing cellular reaction

14. 3) Enzymatic Proteins – Carry out enzymatic reactions right at the membrane when a substrate binds to the active site

15. 4) Cell Recognition Proteins – Glycoproteins (and glycolipids) on extracellular surface serve as ID tags (which species, type of cell, individual). Carbohydrates are short branched chains of less than 15 sugars

16. 5) Attachment Proteins -Attach to cytoskeleton (to maintain cell shape and stabilize proteins) and/or the extracellular matrix (integrins connect to both). -Extracellular Matrix – protein fibers and carbohydrates secreted by cells and fills the spaces between cells and supports cells in a tissue. -Extracellular matrix can influence activity inside the cell and coordinate the behavior of all the cells in a tissue.

17. 6) Intercellular Junction Proteins – Bind cells together –Tight junctions –Gap junctions

18. Materials must move in and out of the cell through the plasma membrane.Materials must move in and out of the cell through the plasma membrane. Some materials move between the phospholipids.Some materials move between the phospholipids. Some materials move through the proteins.Some materials move through the proteins. How do materials move into and out of the cell?

19. Plasma Membrane Transport Molecules move across the plasma membrane by:Molecules move across the plasma membrane by:

20. What are three types of passive transport? 1)Diffusion 2)Facilitated Diffusion 3)Osmosis ATP energy is not needed to move the molecules through.

21. Passive Transport 1: Diffusion Molecules can move directly through the phospholipids of the plasma membraneMolecules can move directly through the phospholipids of the plasma membrane This is called …

22. What is Diffusion? Diffusion is the net movement of molecules from a high concentration to a low concentration until equally distributed. Diffusion is the net movement of molecules from a high concentration to a low concentration until equally distributed. Diffusion rate is related to temperature, pressure, state of matter, size of concentration gradient, and surface area of membrane. Diffusion rate is related to temperature, pressure, state of matter, size of concentration gradient, and surface area of membrane. http://www.biologycorner.com/resources/diffusion-animated.gif

23. What molecules pass through the plasma membrane by diffusion? Gases (oxygen, carbon dioxide) Gases (oxygen, carbon dioxide) Water molecules (rate slow due to polarity) Water molecules (rate slow due to polarity) Lipids (steroid hormones) Lipids (steroid hormones) Lipid soluble molecules (hydrocarbons, alcohols, some vitamins) Lipid soluble molecules (hydrocarbons, alcohols, some vitamins) Small noncharged molecules (NH 3 ) Small noncharged molecules (NH 3 )

24. Why is diffusion important to cells and humans? Cell respirationCell respiration Alveoli of lungsAlveoli of lungs CapillariesCapillaries Red Blood CellsRed Blood Cells Medications: time- release capsulesMedications: time- release capsules

25. Passive Transport 2: Facilitated Diffusion Molecules can move through the plasma membrane with the aid of transport proteinsMolecules can move through the plasma membrane with the aid of transport proteins This is called …

26. What is Facilitated Diffusion? Facilitated diffusion is the net movement of molecules from a high concentration to a low concentration with the aid of channel or carrier proteins.Facilitated diffusion is the net movement of molecules from a high concentration to a low concentration with the aid of channel or carrier proteins.

27. What molecules move through the plasma membrane by facilitated diffusion? IonsIons (Na +, K +, Cl - ) (Na +, K +, Cl - ) Sugars (Glucose)Sugars (Glucose) Amino AcidsAmino Acids Small water soluble moleculesSmall water soluble molecules Water (faster rate)Water (faster rate)

28. How do molecules move through the plasma membrane by facilitated diffusion? Channel and Carrier proteins are specific:Channel and Carrier proteins are specific: Channel Proteins allow ions, small solutes, and water to passChannel Proteins allow ions, small solutes, and water to pass Carrier Proteins move glucose and amino acidsCarrier Proteins move glucose and amino acids Facilitated diffusion is rate limited, by the number of proteins channels/carriers present in the membrane.Facilitated diffusion is rate limited, by the number of proteins channels/carriers present in the membrane.

29. Specific Types of Facilitated Diffusion  Counter Transport – the transport of two substances at the same time in opposite directions, without ATP. Protein carriers are called Antiports.  Co-transport – the transport of two substances at the same time in the same direction, without ATP. Protein carriers are called Symports.  Gated Channels – receptors combined with channel proteins. When a chemical messenger binds to a receptor, a gate opens to allow ions to flow through the channel.

30. Why is facilitated diffusion important to cells and humans? Cells obtain food for cell respirationCells obtain food for cell respiration Neurons communicateNeurons communicate Small intestine cells transport food to bloodstreamSmall intestine cells transport food to bloodstream Muscle cells contractMuscle cells contract

31. Passive Transport 3: Osmosis Water Molecules can move directly through the phospholipids of the plasma membraneWater Molecules can move directly through the phospholipids of the plasma membrane This is called …

32. What is Osmosis? Osmosis is the diffusion of water through a semipermeable membrane. Water molecules bound to solutes cannot pass due to size, only unbound molecules. Free water molecules collide, bump into the membrane, and pass through.Osmosis is the diffusion of water through a semipermeable membrane. Water molecules bound to solutes cannot pass due to size, only unbound molecules. Free water molecules collide, bump into the membrane, and pass through.

33. Osmosis in action What will happen in the U-tube if water freely moves through the membrane but glucose can not pass?What will happen in the U-tube if water freely moves through the membrane but glucose can not pass? Water moves from side with high concentration of water to side with lower concentration of water. Movement stops when osmotic pressure equals hydrostatic pressure.Water moves from side with high concentration of water to side with lower concentration of water. Movement stops when osmotic pressure equals hydrostatic pressure.

34. Why is osmosis important to cells and humans? Cells remove water produced by cell respiration.Cells remove water produced by cell respiration. Large intestine cells transport water to bloodstreamLarge intestine cells transport water to bloodstream Kidney cells form urineKidney cells form urine

35. Osmosis and Tonicity  Tonicity refers to the total solute concentration of the solution outside the cell.  What are the three types of tonicity? 1)Isotonic 2)Hypotonic 3)Hypertonic

36. Isotonic  Solutions that have the same concentration of solutes as the suspended cell.  What will happen to a cell placed in an Isotonic solution?  The cell will have no net movement of water and will stay the same size.  Ex. Blood plasma has high concentration of albumin molecules to make it isotonic to tissues.

37. Hypotonic  Solutions that have a lower solute concentration than the suspended cell.  What will happen to a cell placed in a Hypotonic solution?  The cell will gain water and swell.  If the cell bursts, then we call this lysis. (Red blood cells = hemolysis)  In plant cells with rigid cell walls, this creates turgor pressure.

38. Hypertonic  Solutions that have a higher solute concentration than a suspended cell.  What will happen to a cell placed in a Hypertonic solution?  The cell will lose water and shrink. (Red blood cells = crenation)  In plant cells, the central vacuole will shrink and the plasma membrane will pull away from the cell wall causing the cytoplasm to shrink called plasmolysis.

39. Review: Passive Transport Diffusion – O 2 moves in and CO 2 moves out during cell respirationDiffusion – O 2 moves in and CO 2 moves out during cell respiration Facilitated Diffusion – glucose and amino acids enter cell for cell respirationFacilitated Diffusion – glucose and amino acids enter cell for cell respiration Osmosis – cell removal or addition of waterOsmosis – cell removal or addition of water

40. Review Tonicity  What will happen to a red blood cell in a hypertonic solution?  What will happen to a red blood cell in an isotonic solution?  What will happen to a red blood cell in a hypotonic solution?

41. 1) Active Transport 2) Exocytosis 3) Endocytosis –Phagocytosis –Pinocytosis –Receptor-Mediated endocytosis What are three types of Active transport? ATP energy is required to move the molecules through.

42. Active Transport  Molecules move from areas of low concentration to areas of high concentration with the aid of ATP energy.  Requires protein carriers called Pumps.

43. The Importance of Active Transport  Bring in essential molecules: ions, amino acids, glucose, nucleotides  Rid cell of unwanted molecules (Ex. sodium from urine in kidneys)  Maintain internal conditions different from the environment  Regulate the volume of cells by controlling osmotic potential  Control cellular pH  Re-establish concentration gradients to run facilitated diffusion. (Ex. Sodium-Potassium pump and Proton pumps)

44. The Sodium-Potassium Pump  3 Sodium ions move out of the cell and then 2 Potassium ions move into the cell.  Driven by the splitting of ATP to provide energy and conformational change to proteins by adding and then taking away a phosphate group.  Used to establish an electrochemical gradient across neuron cell membranes. http://www.biologie.uni-hamburg.de/b-online/library/biology107/bi107vc/fa99/terry/images/ATPpumA.gif

45. Active Transport 2: Exocytosis  Movement of large molecules bound in vesicles out of the cell with the aid of ATP energy. Vesicle fuses with the plasma membrane to eject macromolecules.  Ex. Proteins, polysaccharides, polynucleotides, whole cells, hormones, mucus, neurotransmitters, waste

46. Active Transport 3: Endocytosis  Movement of large molecules into the cell by engulfing them in vesicles, using ATP energy.  Three types of Endocytosis: –Phagocytosis –Pinocytosis –Receptor-mediated endocytosis

47. Phagocytosis  “Cellular Eating” – engulfing large molecules, whole cells, bacteria  Ex. Macrophages ingesting bacteria or worn out red blood cells.  Ex. Unicellular organisms engulfing food particles.

48. Pinocytosis  “Cellular Drinking” – engulfing liquids and small molecules dissolved in liquids; unspecific what enters.  Ex. Intestinal cells, Kidney cells, Plant root cells

49. Receptor-Mediated Endocytosis  Movement of very specific molecules into the cell with the use of vesicles coated with the protein clathrin.  Coated pits are specific locations coated with clathrin and receptors. When specific molecules (ligands) bind to the receptors, then this stimulates the molecules to be engulfed into a coated vesicle.  Ex. Uptake of cholesterol (LDL) by animal cells

50. Review Types of Endocytosis  What is phagocytosis?  What is pinocytosis?  What is receptor- mediated endocytosis?

51. Types of Cell Junctions In Animal Cells:  Tight Junctions  Desmosomes  Gap Junctions In Plant Cells:  Plasmodesmata

52. Tight Junctions  Transmembrane Proteins of opposite cells attach in a tight zipper-like fashion  No leakage  Ex. Intestine, Kidneys, Epithelium of skin

53. Desmosomes  Cytoplasmic plaques of two cells bind with the aid of intermediate filaments of keratin  Allows for stretching  Ex. Stomach, Bladder, Heart

54. Gap Junctions  Channel proteins of opposite cells join together providing channels for ions, sugars, amino acids, and other small molecules to pass.  Allows communication between cells.  Ex. Heart muscle, animal embryos

55. Plasmodesmata  Channels between the cell walls of plant cells that are lined with the plasma membranes of adjacent cells and smooth ER runs through.  Allows for the exchange of cytosol between adjacent cells; moving water, small solutes, sugar, and amino acids.  Ex. Xylem and Phloem in Plants

56. Review Types of Cell Junctions  What is the difference between a plasmodesmata, tight junction, gap junction, and desmosome?

57. References Campbell, Neil A., Jane B. Reece, and Lawrence G. Mitchell. (1999). Biology. Reading: Addison Wesley Longman, Inc. Mader, Sylvia S. (1996). Biology. Boston: Times Mirror Higher Education Group, Inc. Raven, Peter H. and Johnson, George B. (1989). Biology. Boston: TimesMirror/Mosby College Publishing.

58. Mitochondria

59. What is a Mitochondrion?  A cellular organelle probably of endosymbiotic origin that resides in the cytosol of most nucleated (eurkaryotic) cells.  This organelle produces energy by oxidising organic acids and fats with oxygen by the process of oxidative phosphorylation and generates oxygen radicals (reactive oxygen species ROS )as a toxic by-product

60. Mitochondrial Structure (cont.)

61. Mitochondrial Genetics  Each cell contains many mitochondria, each of which contains multiple copies of 16.5-k-b circular DNA molecule  The mitochondrial genome is subject to a number of peculiarities of inheritance

62. Number of Mitochondria per cell  Most somatic cells 100-10,000  Lymphocyte1000  Oocytes 100,000  Sperm few hundred  No mitochondria in red cells and some terminally differentiated skin cells

63. Mitochondrial Genetics  Interest in mitochondrial genetics comes mostly from:  interest in diseases caused by mutations in mDNA  interest in human history

65. Mitochondrial Structure

66. 4 444

67. Oxidative phosphorylation

72. Endoplasmic Reticulum

76. A. Functions of the rER Proteins synthesized on ribosomes of rER include: secreto ry proteins, integral membrane proteins, soluble proteins of organelles.

77. A. Functions of the rER Proteins synthesized on ribosomes of rER include: secretory proteins, integral membrane proteins, soluble proteins of organelles

78. Golgi apparatus

80. Golgi complex and cell’s secretion

84. Acrosomal, Cortical Reactions

86. ribosomes 