CHAPTER 12 Membrane Structure and Function. Biological Membranes are composed of Lipid Bilayers and...

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CHAPTER 12 Membrane Structure and Function

Transcript of CHAPTER 12 Membrane Structure and Function. Biological Membranes are composed of Lipid Bilayers and...

Page 1: CHAPTER 12 Membrane Structure and Function. Biological Membranes are composed of Lipid Bilayers and Proteins -Biological membranes define the external.

CHAPTER 12Membrane Structure

and Function

Page 2: CHAPTER 12 Membrane Structure and Function. Biological Membranes are composed of Lipid Bilayers and Proteins -Biological membranes define the external.

Biological Membranes are composed of Lipid Bilayers and Proteins

- Biological membranes define the external boundaries of cells and separate compartments within cells.- A biological membrane consists of two layers of lipid molecules AND- proteins embedded in or associated with the lipid bilayer

Figure 12.1

- Lipid bilayers are the structural basis for biological membranes

- Noncovalent interactions among lipid molecules make membranes flexible and self-sealing.

- Polar head groups contact aqueous medium

- Nonpolar tails point toward the interior of membrane

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Membrane Fluidity

This lipid will result in a morefluid membrane at lower temps

Cholesterol helpsdisrupt hydrophobicinteraction of fatty acidchains.

More fluidity

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Figure 12.8 Integral and peripheral membrane proteins

Integral proteins

Peripheral proteins

Peripheral protein

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Examples of Integral membrane proteins

Figure 12.9: bacteriorhodopsinYellow tubes represent a-helices.light harvesting protein

Figure 12.10-porin, a pore or channelacross the membrane. Note the b-sheet 2o structure

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Examples of peripheral membrane proteins

Figure 12.11: prostaglandin H2 synthase-1

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Lipid Bilayers and Membranes are Dynamic Structures

Figure 12.15

Billion times slower

~2 mm is1 sec

- Some anchored proteins can diffuse laterally just as rapidly as a phospholipid.

- Membrane fluidity is maintained at lower temperaturesby adjusting the ratio of saturated and unsaturated fattyacyl groups

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Membrane Transport

- Membranes are selectively permeable barriers that restrictthe free passage of most molecules

How then do molecules and ions traverse the membrane bilayer?

Through three types of integral membrane proteins:

1. Channels and pores

2. Passive transporters

3. Active transporters

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Passive Transport- Passive transport is called facilitated diffusion because it does

NOT require an energy source

- Transport would otherwise be very slow in absence of protein

- Protein binds solutes and transports them down a concentrationgradient

Types of passive transport systems

- Uniport – transporter carries only a single type of solute

- Some transporters carry out co-transport of two solutes:- Symport – same direction- Antiport – opposite directions

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Figure 12.19Types of passive transport

Uniport

- Passive transport is called facilitated diffusion because it doesNOT require an energy source

- Transport would otherwise be very slow in absence of protein

- Protein binds solutes and transports them down a concentration gradient

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Active Transport- Active transport is similar to passive transport BUT requires

energy to move a solute up its concentration gradient

- Active transport of charged molecules or ions may result in a charge gradient across the membrane. Transport againsta membrane potential (or voltage).

Types of active transport

- Primary active transport is powered by a direct source of energyas ATP, light or electron transport

- Secondary active transport is driven by an ion concentration gradient.

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Figure 12.16 Primary active transport in animals: Na+/K+ ATPase Pump

- An ATP driven antiport transport

Exterior:[K+] = 5mM[Na+] = 145 mM

Cytosol:[K+] = 140mM[Na+] = 5-15 mM

> 30% of ATP generated is used to maintainthis gradient and that’s when resting!

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Figure 12.20. The ATPase pump drives a secondary activetransport (symport) of glucose into cell.

antiport

Na+ ion gradient

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Pores and Channels(pores are used for bacteria and channels for animals)

- Pores and channels are trans-membrane proteins with a centralpassage for diffusion of ions and small molecules

- Passage can be in either direction and is very fast relative to pumps.

- Solutes of appropriate size, charge, molecular structure (geometry) can diffuse down a concentration gradient

- Process requires no energy

- Are selective for specific solutes based on conditions to traverse the membrane

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Figure 12.22. The K+ ion channel

K+ ion flow

K+ ions still solvatedby water

K+ ions desolvated

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Figure 12.23. The K+ ion channel

Note the peptide carbonyl groups interacting with the K+

ions in the 3 Å region.

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Figure 12.24. The K+ ion channel

More energy is released (exothermic) in resolvation in channelthan the cost of desolvation of water (endothermic).

This is why the channel is selective for K+

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Figure 12.24. The K+ ion channel

Na+ ions aresmaller thanK+ ions

Why don’t Na+ ions traversethe K+ channel??

More energy is needed (endothermic) in desolvation of water in channel than released during resolvation within the channel.

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Figure 12.25. The K+ ion channel

Hydrated K+ ions

Repulsion of adjacent K+ ion is channel pushes theions through the channel.

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Endocytosis and Exocytosis

How do cells import/export molecules too large for transport via pores, channels or transport proteins?

Endocytosis – macromolecules are engulfed by plasma membrane and brought into the cell inside a lipid vesicle

Exocytosis – materials to be excreted from the cell are enclosed in vesicles that fuse with the plasma membraneand release the vesicle contents into the extracellular space

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Assignment

Read Chapter 11Read Chapter 12

Read Clinical Insight Page 201