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Membrane Structure and Function ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Figure 7.1
[object Object],[object Object],Figure 7.2 Hydrophilic head Hydrophobic tail WATER WATER
The Fluidity of Membranes ,[object Object],[object Object],Figure 7.5 A Lateral movement (~10 7  times per second)  Flip-flop (~ once per month) (a) Movement of phospholipids
[object Object],[object Object],Figure 7.5  B Fluid Viscous Unsaturated hydrocarbon tails with kinks Saturated hydro- Carbon tails (b) Membrane fluidity
[object Object],[object Object],Figure 7.5  (c) Cholesterol within the animal cell membrane Cholesterol
Membrane Proteins and Their Functions ,[object Object],[object Object],Fibers of extracellular matrix (ECM) Figure 7.7 Glycoprotein Carbohydrate Microfilaments of cytoskeleton Cholesterol Peripheral protein Integral protein CYTOPLASMIC SIDE OF MEMBRANE EXTRACELLULAR SIDE OF MEMBRANE Glycolipid
[object Object],[object Object],[object Object],EXTRACELLULAR SIDE Figure 7.8 N-terminus C-terminus    Helix CYTOPLASMIC SIDE
[object Object],Figure 7.9  Transport. (left)  A protein that spans the membrane may provide a hydrophilic channel across the membrane that is selective for a particular solute. (right)  Other transport proteins shuttle a substance from one side to the other by changing shape. Some of these proteins hydrolyze ATP as an energy ssource to actively pump substances  across the membrane. Enzymatic activity.  A protein built into the membrane may be an enzyme with its active site exposed to substances in the adjacent solution. In some cases, several enzymes in a membrane are organized as a team that carries out sequential steps of a metabolic pathway. Signal transduction.  A membrane protein may have a binding site with a specific shape that fits the shape of a chemical messenger, such as a hormone. The external messenger (signal) may cause a conformational change in the protein (receptor) that relays the message to the inside of the cell. (a) (b) (c) ATP Enzymes Signal Receptor
Cell-cell recognition.  Some glyco-proteins serve as  identification tags that are specifically recognized  by other cells.  Intercellular joining.  Membrane proteins of adjacent cells may hook together in various kinds of junctions, such as gap junctions or tight junctions (see Figure 6.31). Attachment to the cytoskeleton and extracellular matrix (ECM).  Microfilaments or other elements of the cytoskeleton may be bonded to membrane proteins, a function that helps maintain cell shape and stabilizes the location of certain membrane proteins. Proteins that adhere to the ECM can coordinate extracellular and intracellular changes (see Figure 6.29). (d) (e) (f) Glyco- protein Figure 7.9
The Role of Membrane Carbohydrates in Cell-Cell Recognition ,[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],ER Figure 7.10 Transmembrane glycoproteins Secretory protein Glycolipid Golgi apparatus Vesicle Transmembrane glycoprotein Membrane glycolipid Plasma membrane: Cytoplasmic face Extracellular face Secreted protein 4 1 2 3
[object Object],[object Object]
The Permeability of the Lipid Bilayer ,[object Object],[object Object],[object Object],[object Object]
Transport Proteins ,[object Object],[object Object]
[object Object]
[object Object],[object Object],Figure 7.11 A Diffusion of one solute.  The membrane  has pores large enough for molecules  of dye to pass through. Random  movement of dye molecules will cause  some to pass through the pores; this  will happen more often on the side  with more molecules. The dye diffuses  from where it is more concentrated  to where it is less concentrated  (called diffusing down a concentration  gradient). This leads to a dynamic  equilibrium: The solute molecules  continue to cross the membrane,  but at equal rates in both directions. Molecules of dye Membrane (cross section) Net diffusion Net diffusion Equilibrium (a)
[object Object],Figure 7.11 B Diffusion of two solutes.  Solutions of  two different dyes are separated by a  membrane that is permeable to both.  Each dye diffuses down its own concen- tration gradient. There will be a net  diffusion of the purple dye toward the  left, even though the  total  solute concentration was initially greater on the left side. (b) Net diffusion Net diffusion Net diffusion Net diffusion Equilibrium Equilibrium
Effects of Osmosis on Water Balance ,[object Object],[object Object]
[object Object],Figure 7.12 Lower concentration of solute (sugar) Higher concentration of sugar Same concentration of sugar Selectively permeable mem- brane: sugar mole- cules cannot pass through pores, but water molecules can More free water molecules (higher concentration) Water molecules cluster around  sugar molecules Fewer free water molecules (lower concentration) Water moves from an area of higher  free water concentration to an area  of lower free water concentration  Osmosis
Water Balance of Cells Without Walls ,[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object]
[object Object],Figure 7.13  Hypotonic solution Isotonic solution Hypertonic solution Animal cell.  An animal cell fares best in an isotonic environ- ment unless it has special adaptations to offset the osmotic uptake or loss of water. (a) H 2 O H 2 O H 2 O H 2 O Lysed Normal Shriveled
[object Object],[object Object],H 2 O Figure 7.13  Hypotonic solution Isotonic solution Hypertonic solution Animal cell. An animal cell fares best in an isotonic environ- ment unless it has special adaptations to offset the osmotic uptake or loss of water. (a) H 2 O H 2 O H 2 O Lysed Normal Shriveled
Water Balance of Cells with Walls ,[object Object],[object Object]
[object Object],[object Object],[object Object]
[object Object],[object Object]
[object Object],Plant cell.  Plant cells  are turgid (firm) and  generally healthiest in a hypotonic environ- ment, where the uptake of water is eventually balanced by the elastic wall pushing back on the cell. (b) H 2 O H 2 O H 2 O H 2 O Turgid (normal) Flaccid Plasmolyzed Figure 7.13
Facilitated Diffusion: Passive Transport Aided by Proteins ,[object Object],[object Object]
[object Object],[object Object],Figure 7.15  EXTRACELLULAR FLUID Channel protein Solute CYTOPLASM A channel protein (purple) has a channel through which  water molecules or a specific solute can pass. (a)
[object Object],[object Object],Figure 7.15  Carrier protein Solute A carrier protein alternates between two conformations, moving a  solute across  the membrane as the shape of the protein changes.  The protein can transport the solute in either direction, with the net  movement being down the concentration gradient of the solute. (b)
[object Object]
The Need for Energy in Active Transport ,[object Object],[object Object],[object Object]
[object Object],[object Object],Figure 7.16 P P  i EXTRACELLULAR FLUID 4 5 6 3 Na+ binding stimulates phosphorylation by ATP. 2 Na + Cytoplasmic Na +  binds to the sodium-potassium pump. 1 K +  is released and Na + sites are receptive again;  the cycle repeats. 3 Phosphorylation causes the  protein to change its conformation, expelling Na +  to the outside. Extracellular K +  binds to the  protein, triggering release of the  Phosphate group. Loss of the phosphate restores the protein’s  original conformation. CYTOPLASM [Na + ] low [K + ] high Na + Na + Na + Na + Na + P ATP Na + Na + Na + P ADP K + K + K + K + K + K + [Na + ] high [K + ] low
Recap
[object Object],Figure 7.17 Passive transport . Substances diffuse spontaneously  down their concentration gradients, crossing a  membrane with no expenditure of energy by the cell.  The rate of diffusion can be greatly increased by transport  proteins in the membrane. Active transport . Some transport proteins act as pumps, moving substances across a membrane against their concentration gradients. Energy for this work is usually supplied by ATP. Diffusion.  Hydrophobic molecules and (at a slow  rate) very small uncharged  polar molecules can diffuse through the lipid bilayer. Facilitated diffusion.  Many hydrophilic substances diffuse through membranes with the assistance of transport proteins, either channel or carrier proteins. ATP
Maintenance of Membrane Potential by Ion Pumps ,[object Object],[object Object]
[object Object],[object Object],Figure 7.18 EXTRACELLULAR FLUID + H + H + H + H + H + H + Proton pump ATP CYTOPLASM + + + + – – – – – +
[object Object],Co-transport , also known as coupled transport, refers to the simultaneous or sequential passive transfer of molecules or ions across biological membranes in a  fixed ratio . Permitting one ion or molecule to move from the side where it is more concentrated to that where it is less concentrated increases entropy and can serve as a source of energy for metabolism (e.g. in ATP synthase). In cotransporters, it is used to force the transport of another ion or molecule (usually) from the side where it is less concentrated to that where it is more concentrated .  Figure 7.19 Proton pump Sucrose-H + cotransporter Diffusion of H + Sucrose ATP H + H + H + H + H + H + H + + + + + + + – – – – – –
[object Object],[object Object],[object Object]
Exocytosis ,[object Object],[object Object]
Endocytosis ,[object Object],[object Object]
[object Object],In  phagocytosis,  a cell engulfs a particle by  Wrapping pseudopodia  around it and packaging  it within a membrane- enclosed sac large  enough to be classified  as a vacuole. The  particle is digested after  the vacuole fuses with a  lysosome containing  hydrolytic enzymes.  Figure 7.20 PHAGOCYTOSIS EXTRACELLULAR FLUID Pseudopodium CYTOPLASM “ Food” or  other particle Food vacuole 1 µm Pseudopodium of amoeba Bacterium Food vacuole An amoeba engulfing a bacterium via phagocytosis (TEM). PINOCYTOSIS Pinocytosis vesicles forming (arrows) in a cell lining a small blood vessel (TEM). 0.5 µm In  pinocytosis,  the cell  “ gulps” droplets of  extracellular fluid into tiny vesicles. It is not the fluid itself that is needed by the  cell, but the molecules  dissolved in the droplet.  Because any and all  included solutes are taken  into the cell, pinocytosis is nonspecific in the  substances it transports. Plasma membrane Vesicle
0.25 µm RECEPTOR-MEDIATED ENDOCYTOSIS Receptor Ligand Coat protein Coated pit Coated vesicle A coated pit and a coated vesicle formed during receptor- mediated endocytosis (TEMs). Plasma membrane Coat protein Receptor-mediated endocytosis  enables the  cell to acquire bulk quantities of specific  substances, even though those substances  may not be very concentrated in the  extracellular fluid. Embedded in the  membrane are proteins with  specific receptor sites exposed to  the extracellular fluid. The receptor proteins are usually already clustered  in regions of the membrane called coated  pits, which are lined on their cytoplasmic  side by a fuzzy layer of coat proteins.  Extracellular substances (ligands) bind  to these receptors. When binding occurs,  the coated pit forms a vesicle containing the  ligand molecules. Notice that there are  relatively more bound molecules (purple)  inside the vesicle, other molecules  (green) are also present. After this ingested  material is liberated from the vesicle, the  receptors are recycled to the plasma  membrane by the same vesicle.
Water Potential ,[object Object],Water always moves from an area of higher water potential  (higher free energy) to an area of lower water potential (lower free energy). An  increase in solute potential  makes the  water potential more negative  and an  increase in pressure potential  makes the  water potential more positive.
Water Potential ,[object Object]

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07 membranes text

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  • 9. Cell-cell recognition. Some glyco-proteins serve as identification tags that are specifically recognized by other cells. Intercellular joining. Membrane proteins of adjacent cells may hook together in various kinds of junctions, such as gap junctions or tight junctions (see Figure 6.31). Attachment to the cytoskeleton and extracellular matrix (ECM). Microfilaments or other elements of the cytoskeleton may be bonded to membrane proteins, a function that helps maintain cell shape and stabilizes the location of certain membrane proteins. Proteins that adhere to the ECM can coordinate extracellular and intracellular changes (see Figure 6.29). (d) (e) (f) Glyco- protein Figure 7.9
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  • 36. Recap
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  • 45. 0.25 µm RECEPTOR-MEDIATED ENDOCYTOSIS Receptor Ligand Coat protein Coated pit Coated vesicle A coated pit and a coated vesicle formed during receptor- mediated endocytosis (TEMs). Plasma membrane Coat protein Receptor-mediated endocytosis enables the cell to acquire bulk quantities of specific substances, even though those substances may not be very concentrated in the extracellular fluid. Embedded in the membrane are proteins with specific receptor sites exposed to the extracellular fluid. The receptor proteins are usually already clustered in regions of the membrane called coated pits, which are lined on their cytoplasmic side by a fuzzy layer of coat proteins. Extracellular substances (ligands) bind to these receptors. When binding occurs, the coated pit forms a vesicle containing the ligand molecules. Notice that there are relatively more bound molecules (purple) inside the vesicle, other molecules (green) are also present. After this ingested material is liberated from the vesicle, the receptors are recycled to the plasma membrane by the same vesicle.
  • 46.
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