Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from...

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Chapter 7: Membrane Structure & Function • Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): • Observation: Lipid and lipid soluble materials enter cells most rapidly • Deduction: Membranes are made of lipids

Transcript of Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from...

Page 1: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Chapter 7: Membrane Structure & Function

• Early models of the plasma membrane were deduced from indirect evidence.

1. Charles Overton (1895): • Observation: Lipid and lipid soluble materials

enter cells most rapidly • Deduction: Membranes are made of lipids

Page 2: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

2. Irving Langmuir (1917): • Observation: Amphipathic phospholipids will

form an artificial membrane on the surface of water

• Deduction: phospholipids can form

membranes.

Page 3: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

3. Gorter and Grendel (1925): • Observation: Phospholipid content of membranes

isolated from red blood cells is just enough to cover cells with two layers.

• Deduction: Cell membranes are phospholipid bilayers • Observation: Membranes isolated from red blood cells

contain proteins as well as lipids. • Deduction: There is protein in biological membranes

Page 4: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

4. Hugh Davson and James Daneilli (1935)

The cell membrane is a phospholipid bilayer sandwiched between two layers of globular

protein

The membrane is approximately 8 nm thick

Page 5: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

5. In 1972, S.J. Singer and G.L. Nicolson proposed the fluid mosaic model

Proteins are individually embedded in the phospholipid bilayer (not a solid surface coat) Hydrophilic portions of both proteins and phospholipids are maximally exposed to water Hydrophobic portions of proteins are phospholipids are in the nonaqueous environment inside the bilayer. The membrane is a mosaic of proteins bobbing in a fluid bilayer of phospholipids.

Page 6: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

a membrane is a fluid mosaic of lipids, proteins, and carbohydrates.

Membranes are held together by hydrophobic interactions and most membrane lipids and some

proteins can drift laterally within the membrane. Membranes must be fluid to work properly. Solidification may result in permeability changes and enzyme deactivation. Unsaturated hydrocarbon tails enhance membrane fluidity –why?

Page 7: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Cholesterol, found in plasma membranes of animal eukaryotes, modulates membrane fluidity by making the membrane:

• less fluid at warmer temperatures (e.g. 37C body temp) by restraining phospholipids movement

• more fluid at lower temperatures by preventing close packing of phospholipids.

Cells may alter membrane lipid concentration in response to changes in temperature.

Many cold tolerant plants (e.g. winter wheat) increase the unsaturated phospholipids concentration in the autumn to maintain membrane fluidity

Page 8: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

The proteins found in the phospholipid bilayer vary in both structure and function

• Integral proteins are embedded in the membrane– Unilateral – reaching only partway across the

membrane– Transmembrane – exposed on both sides of the

membrane.

• Peripheral proteins are not embedded, but are attached to the membrane’s surface (cytoplasmic side )

Page 9: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Protein functions1. Cell to cell recognition 2. enzymatic activity 3- signal transduction 4- intercellular (hormones) joining5- attachment to ECM

6-Cell Transport: Selective permeability – property of biological

membrane which allows some substances to cross more easily than others. depends on:

• Phospholipid solubility characteristics• presence of specific integral transport proteins

Page 10: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Solubility characteristics: (from artificial membrane only)

Nonpolar and hydrophobic molecules dissolve in the membrane and cross it with ease (e.g. hydrocarbons and oxygen)

Polar (hydrophilic) molecules are dependent on size and charge Small molecules (e.g. H2O, CO2) may be small enough to pass between membrane lipids Larger molecules (e.g. glucose) will not easily pass

IONS- even small ones (e.g. Na+, H+) have difficulty penetrating the hydrophobic layer.

Water, CO2, and nonpolar molecules rapidly pass through the plasma membrane as they do an artificial membrane.

Page 11: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Transport proteins

integral transmembrane proteins that transport specific molecules or ions across biological membranes. Are highly specific for the substance they translocate May provide a hydrophilic tunnel May bind to a substance and physically move it across

Page 12: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Passive Transport

diffusion of a substance across a biological membrane•does not require the cell to expend energy. •Driven by concentration gradient Rate is regulated by the permeability of the membrane Water diffuses freely across most cell membranes

Page 13: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Osmosis – diffusion of water across a selectively permeable membrane

Water diffuses down its concentration gradient.

Page 14: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

• Hypertonic solution – a solution with a greater solute concentration than that inside the cell

• Hypotonic solution – a solution with a lower solute concentration than that inside the cell.

• Isotonic solution – a solution with an equal solute concentration compared to that inside the cell.

• U-tube If two isosmotic solutions are separated by a selectively permeable membrane, water molecules diffuse across the membrane in both directions at an equal rate. However, there is no NET movement of water.

Page 15: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Water potential – measure of the tendency for a solution to take up water by a selectively permeable membrane.

Water potential of pure water is zero.- Solutes lower the water potential (ex -2)- Water flows from HIGH to LOW (water

potential)

- Water flows from hypertonic to hypertonic

Page 16: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Water Balance of Cells Without Walls

In a hypertonic environment, an animal cell will lose water by osmosis and shrivel.

In a hypotonic environment, an animal cell will gain water by osmosis, swell, and perhaps lyse (burst).

Page 17: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Organisms without cell walls prevent excessive loss or uptake of water by:

Living in an isotonic environment Osmoregulating

Page 18: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Water Balance of Cells With Walls prokaryotes, some protists, fungi, and plants

• In a hypertonic environment, walled cells will

lose water by osmosis and will plasmolyze, which is usually lethal.

Plasmolysis = plasma membrane pulls away from the cell wall as the cell loses water to a hypertonic environment.

Page 19: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

In a hypotonic environment, water moves by osmosis into the plant cell, causing it to swell until internal pressure against the cell wall equals the osmotic pressure of the cytoplasm.

Creates turgid cells = ideal for support Turgidity is the firmness or tension found in

walled cells.

Page 20: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

In an isotonic environment, there is no net movement of water into or out of the cell and the plant cells become flaccid (limp).

Loss of structural support from decreased turgid pressure causes plants to wilt.

Page 21: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Facilitated diffusion

– diffusion of solutes across a membrane with the help of transport proteins.

A passive transport down the concentration gradient

Helps the diffusion of many polar molecules and ions which are impeded by the membrane’s phospholipid bilayer.

Page 22: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Transport proteins share some properties of enzymes:

• are specific for the solutes they transport. - analogous to an enzyme’s active site.• can be saturated with solute = maximum

transport rate occurring• can be inhibited by molecules that resemble the

normal solute ( resembles competitive inhibition in enzymes).

• However, they do not usually catalyze chemical

reactions.

Page 23: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

One Model for Facilitated Diffusion: Transport proteins forms a channel through

which water molecules or specific solutes can pass. (Aquaporins are water channels)

• Some proteins are gated channels and only open in response to electrical or chemical stimuli. (neurotransmitters and neurons)

Page 24: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Second Model for Facilitated Diffusion: Transport protein most likely remains in place in the membrane and translocates solute by alternating between two conformations. In one conformation, the transport protein binds the solute; in the second conformation, it deposits the solute on the other side of the membrane. The protein can transport in either direction, with the

net movement being down the concentration gradient

Page 25: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Active Transport

• ATP requiring process during which a transport protein pumps a molecule across a membrane against its concentration gradient.

Helps cells maintain steep ionic gradients across the cell membrane (e.g. Na+, Cl-)

Page 26: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Sodium-potassium pump: (example of active transport)

– Na+ binding sites on the cytoplasm side and K+ binding sites on the cell exterior

• ATP phosphorylates the transport protein and powers the conformational change from Na+ receptive to K+ receptive

• As the transport protein changes conformation, it translocates bound solutes across the membrane

• three Na+ ions out of the cell for every two K+ pumped into the cell creates a polarized membrane

Page 27: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Electrochemical gradient – diffusion gradient resulting from the combined effects of membrane potential and concentration gradient

Ions always diffuse down their electrochemical gradients

Uncharged solutes diffuse down concentration gradients only

Page 28: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Electrogenic pump – a transport protein that generates voltage across a

membrane• Na+/K+ pump is the major electrogenic pump

in animals * A proton pump is the major electrogenic

pump in plants, bacteria, and fungi. Also, mitochondria and chloroplasts use proton pumps for syntheis of ATP

electrogenic pumps are sources of potential energy

Page 29: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Exocytosis and Endocytosis

Exocytosis – process of exporting macromolecules from a cell by fusion of vesicles with the plasma membrane Vesicle usually buds from the ER or Golgi and migrates to the plasma membrane. Used by secretory cells of pancreas (insulin) or neurons (neurotransmitters) Endocytosis – process of importing macromolecules into a cell by forming vesicles derived from the plasma membrane Vesicle forms from a localized region of the plasma

membrane that sinks inward (pinches off)

Page 30: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

three types of endocytosis:

Phagocytosis – endocytosis of solid particles amoeba engulfs particle with pseudopodia and forms a food vacuole. WBC’s do this too

Pinocytosis – endocytosis of fluid droplets taken in as small vesicles.

Page 31: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Receptor-mediated endocytosis – process of importing specific macromolecules into the cells in response to the binding of specific ligands to receptors on the cell’s surface Ligand is a generic term for a molecule that binds to a receptor site of another molecule A very discriminating process

Page 32: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

Stages of Receptor-Mediated Endocytosis: Extracellular ligand binds to receptors in a coated pitCauses inward budding of the coated pitForms a coated vesicleIngested material is released from the vesicleProtein receptors are recycled to the plasma membrane

Page 33: Chapter 7: Membrane Structure & Function Early models of the plasma membrane were deduced from indirect evidence. 1. Charles Overton (1895): Observation:

enables cells to acquire bulk quantities of specific substances, even if they are in low concentration in extracellular fluid. In the blood, cholesterol is bound to low-density lipoproteins (LDLs) These LDLs bind to LDL receptors on cell membranes defective LDL receptors can lead to atherosclerosis.