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What is the Structure of the Cell Membrane?

What is the Structure of the Cell Membrane?. Constituents Phospholipids : molecule consists of two hydrocarbon chains ( hydrophobic ) and phosphate group ( hydrophilic ) Proteins

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What is the Structure of the Cell Membrane?

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  1. What is the Structure of the Cell Membrane? • Constituents • Phospholipids: molecule consists of two hydrocarbon chains (hydrophobic) and phosphate group (hydrophilic) • Proteins • Integral proteins: embedded in lipids; some cross entire membrane, often act like gates (allow substances into/out of cell) • Peripheral proteins: along edge of membrane (inside or outside); often receptors for hormones; entire complex moves into cell • Cholesterol: maintains fluidity of membrane • Carbohydrate Chains: found on outside of cell; involved in cell to cell recognition and hormone reception • The Fluid-Mosaic Model: fluid bi-layer; lipids internalized in membrane

  2. Figures 7.2 and 7.3

  3. Figures 5.13a and 5.13b

  4. Figure 7.7

  5. Figure 7.9

  6. How do Substances Get Into or Out Of Cells? • Passive Transport • Diffusion: spread of substance along a concentration gradient (from high to low concentrations) • Only small, neutral molecules can pass through membrane (ex. O2, CO2) • Osmosis: diffusion of water across a cell membrane • Facilitated Transport • Molecule or ion crosses membrane via carrier/gate protein, following a concentration gradient (no energy expenditure required) • Active Transport • Molecule or ion crosses membrane via carrier/gate protein, against a concentration gradient (energy expenditure) • Endocytosis/Exocytosis (requires energy expenditure) • Endo: molecules enveloped by cell membrane  vesicle into cell • Exo: molecules produced in cell excreted via vesicle

  7. Figure 7.12

  8. Figure 7.13

  9. Figure 7.15

  10. Figure 7.16

  11. Figure 7.18

  12. Figure 7.20

  13. Figure 7.20 (cont.)

  14. Figure 7.10

  15. How is Energy Involved in Cellular Metabolism? • ATP and Metabolism • Energy required for many cellular reactions, including active transport, endo- and exocytosis, biosynthesis, and mechanical work/movement • Energy transferred from exothermic to endothermic reactions via adenosine triphosphate (ATP), the universal energy currency • Overview of Catabolic Processes • Stage I: Hydrolysis of Dietary Macromolecules into Small Subunits • Starch  maltose  glucose, catalyzed by amylase and maltase • Proteins denatured by stomach acid, digested by pepsin and various protease enzymes • Emulsion of fats by bile salts; hydrolysis by lipase • Stage II: Conversion of Monomers to Forms That Can Be Fully Oxidized • Monomers enter either glycolysis or the Krebs Cycle • Stage III: Complete Oxidation of Compounds and the Production of ATP

  16. Figure 8.6

  17. Figure 8.5

  18. Figures 8.8 and 8.9

  19. Figure 8.12

  20. How are Enzymes Involved in Cellular Metabolism? • Importance of Shape and Structure with Proteins • Cellular functions related to shape and intact structures of proteins • Denaturation: loss of 3° and/or 4° structures; can be caused by excess temperature, pH changes, chemicals, or mechanical stress • Enzymes: biological catalysts; most are proteins • Increase rates of chemical reactions; reduce activation energy; each molecule recycled • IUPAC names derive from substrates and actions; end with –ase • Substrate(s) fit in active site(s); induced-fit model favored over lock-and-key model • Often require cofactors (metals, organics) and/or coenzymes

  21. Figure 8.15

  22. Figure 8.16

  23. Figure 8.17

  24. What Factors Affect Enzyme Function? • Effect of pH Levels • Enzymes are only active within narrow pH ranges, and work best at specific pH optima • Most cytoplasmic enzymes require pH of 7; pepsin works best at pH ~2 (in stomach acid) • Some bacteria have evolved to live at extreme pH levels • Effect of Temperature • Enzymes are only active within narrow temperature ranges, and work best at their temperature optima (humans ~37 C) • If too hot, can become denatured; if too cold, reaction rates can be reduced below critical rates • Enzyme Inhibition: compounds block active sites • Irreversible Inhibitors: include arsenic, snake venoms, nerve gases • Competitive Inhibitors: compounds are structural analogues to enzymes’ substrates (the dose makes the poison)

  25. Figure 8.18

  26. Figure 8.19

  27. Figure 8.20b

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