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Membrane Structure and Function Chs. 8 and 11 Cell Membrane – Introduction  Separates the living cell from its nonliving surroundings  8 nm thick  Controls traffic into and out of the cell (selectively permeable)  Composed of lipids (phospholipids) and proteins, but include some carbohydrates Cell Membrane – Introduction  Phospholipids and most other membrane constituents are amphipathic molecules  Amphipathic molecules have both hydrophobic and hydrophilic regions  Described by the fluid mosaic model Membrane Model Development  1895 – Charles Overton; hypothesized membranes made of lipids  Observed lipid-soluble substances move across membrane easier than lipid-nonsoluble substances  1917 – Irving Langmuir;  Dissolved phospholipids in benzene and mixed with water  When benzene evaporated, phospholipid film formed on water  1925 – E. Gorter and F. Grendel concluded membrane must be bilayer of phospholipids  Polar phosphorous head interacts with polar water (hydrophilic)  Nonpolar fatty acid tails are sheltered from the water (hydrophobic)  Experiments showed real membranes attract water stronger than artificial ones  Hypothesis: proteins aid in water attraction  1935 – H. Davson and J. Danielli propose sandwich model: bilayer between layers of proteins  Davson-Danielli model considered dominant, even after EM images  Two problems:  Membranes differed in size, composition, and stained appearance  Membrane proteins are amphipathic; can’t be on surface only Fluid Mosaic Model  1972 – S.J. Singer and G. Nicolson present revised model; hypothesize proteins are distributed throughout and among the bilayer Membranes are fluid  Membrane molecules are not held together by bonds; they can slip/move past/around each other  Evidence: when human and mouse cells are fused together, membrane proteins don’t stay separated.  Most membrane molecules can move laterally; rarely do they flip-flop  Some proteins can’t move; bound to the cytoskeleton  Fluidity influenced by two factors:  Temp: As temp decreases, lipids pack closer together – become more solid  Saturation: unsaturated fatty acid tails make the membrane more fluid  Cholesterol is wedged in the plasma membrane  Warm temps: it restrains the movement of phospholipids and reduces fluidity  Cool temps: it maintains fluidity by preventing tight packing Membranes are mosaics Membranes are mosaics  Membranes each have a unique collections of proteins  Membrane functions determined mostly by proteins  Two types of membrane proteins:  Peripheral proteins: not embedded in lipid bilayer  Integral proteins: penetrate the hydrophobic core of lipid bilayer, often completely spanning the membrane (transmembrane protein) Membranes are mosaics  Membranes have distinctive inside and outside faces The outer surface has carbohydrates This asymmetrical orientation begins during synthesis of new membrane in the endoplasmic reticulum Membranes are mosaics  Membrane protein functions: Cell-Cell Recognition Ability of a cell to distinguish one type of neighboring cell from another The membrane plays the key role in cell-cell recognition Cells recognize other cells from surface molecules, often carbs, on membrane  Glycolipids  Glycoproteins (more common) Cell-Cell Recognition Carbs on external side of membrane vary from species to species, individual to individual, and even from cell type to cell type within the same individual Variation marks each cell type as distinct The four human blood groups (A, B, AB, and O) differ in the external carbohydrates on red blood cells It is also the basis for rejection of foreign cells by the immune system This attribute is important in cell sorting and organization as tissues and organs in development Transport  Membranes act as gatekeepers (selectively permeable)  Select based on size and charge  Small, uncharged atoms/molecules don’t have problems  Large and/or charged atoms/molecules do have problems  Proteins can help transport Transport Proteins  Each transport protein is specific as to the substances that it will translocate  Some act like a channel or tunnel through the membrane  Others bind to their specific molecules and physically carry them across the membrane Passive Transport  No E required  Requires gradient (separation of concentrations)  Movement from areas of Hi to Low (down, along, or with) concentrations  Movement continues even after equilibrium is reached  Rate of diffusion depends on size and charge of molecules (interaction with the membrane) Passive Transport  Simple Diffusion: movement of molecules from Hi to Low concentrations Passive Transport  Each substance diffuses down its own concentration gradient, independent of the concentration gradients of other substances Passive Transport  Osmosis: diffusion of water across a semi-permeable membrane  Osmosis continues until the solutions are isotonic  When two solutions are isotonic, water molecules move at equal rates from one to the other, with no net osmosis Passive Transport  A solution with a higher concentration of solutes is hypertonic  A solution with a lower concentration of solutes is hypotonic  These are comparative terms  Tap water is hypertonic compared to distilled water but hypotonic when compared to sea water  Solutions with equal solute concentrations of solute are isotonic Passive Transport Passive Transport  Paramecia have contractile vacuoles to expel excess water Passive Transport  Facilitated diffusion: diffusion using “helper” molecules  Those atoms and molecules that were too big or charged can still move down their concentration gradient (hi to low) Passive Transport: Facilitated diffusion  Some proteins (channel) act like corridors  Allow for fast, bulk flow  Ex: aquiporins Passive Transport: Facilitated diffusion Some channel proteins (gated channels) open or close depending on the presence or absence of a physical or chemical stimulus The chemical stimulus is usually different from the transported molecule Ex: when neurotransmitters bind to specific gated channels on the receiving neuron, these channels open This allows sodium ions into a nerve cell When the neurotransmitters are not present, the channels are closed Passive Transport: Facilitated diffusion  Some proteins change shape to physically translocate the molecules  These shape changes could be triggered by the binding and release of the transported molecule  Transport proteins are much like enzymes  They may have specific binding sites for the solute  Transport proteins can become saturated when they are translocating passengers as fast as they can  Transport proteins can be inhibited by molecules that resemble the normal “substrate”  When these bind to the transport proteins, they outcompete the normal substrate for transport Active Transport  Requires E (ATP)  Movement of molecules against or up their concentration gradients  Low to Hi  Performed by receptor proteins Active Transport  The sodium-potassium pump actively maintains the gradient of sodium (Na+) and potassium ions (K+) across the membrane  Typically, an animal cell has higher concentrations of K+ and lower concentrations of Na+ inside the cell  The sodium-potassium pump uses the E of one ATP to pump three Na+ out and two K+ in Ions keep separate charges across a membrane  Membrane potential: voltage difference across the membrane  Electrochemical gradient  Gradient due to concentrations of ions  Gradient due to membrane potential  electrogenic pumps generate voltage gradient Ions keep separate charges across a membrane  In plants, bacteria, and fungi, a proton pump is the major electrogenic pump, actively transporting H+ out of the cell  Proton pumps in the cristae of mitochondria and the thylaloids of chloroplasts, concentrate H+ behind membranes  These electrogenic pumps store energy that can be accessed for cellular work. Cotransport  A single ATP-powered pump that transports one solute can indirectly drive the active transport of several other solutes through cotransport via a different protein  As the solute that has been actively transported diffuses back passively through a transport protein, its movement can be coupled with the active transport of another substance against its concentration gradient  Plants commonly use the gradient of H+ that is generated by proton pumps to drive the active transport of amino acids, sugars, and other nutrients into the cell  The high concentration of H+ on one side of the membrane, created by the proton pump, leads to the facilitated diffusion of protons back, but only if another molecule, like sucrose, travels with the H+ Endo- vs. Exocytosis  Both move large molecules into/out of the cell  Both use vesicles  Reverse processes of each other Endocytosis  A small area of the plasma membrane sinks inward to form a pocket  The pocket deepens, pinches in, and forms a vesicle containing the material that had been outside the cell Endocytosis  Two types:  Phagocytosis: cell eating  Pinocytosis: cell drinking  Receptor mediated endocytosis Receptor mediated Endocytosis  Triggered when extracellular substances bind to special receptors, ligands, on membrane surface, especially near coated pits