Notes on Chapter 11

Use these notes as you read the text. These will not be collected, but as you write answers to these questions you will increase your comprehension, and you will be able to better articulate what you don't understand. Comments and suggestions are most welcome!

An introduction to membranes and their lipids.

Words that you should be able to define:

Micelle

Liposome

Bilayer

Important concepts:

Behavior of lipids in aqueous environments

What is the major driving force for the formation of micelles, liposomes and bilayers?

Transition temperature

Look at table 11-2, what generalizations can you make about fatty acid composition and the temperature that was used to culture E. coli?

Role of cholesterol in lipid fluidity

How does it increase fluidity?

How does it decrease fluidity?

Movement of lipids

What is the difference between lateral diffusion of a phospholipid and transbilayer diffusion? What is required for transbilayer diffusion?



Proteins in membranes and membrane fusion.

Words that you should be able to define:

Integral

Peripheral

Annexins

Hydropathy index

Fusion proteins

Integrins (CD18 is the beta subunit of an integrin, defects in this subunit cause leukocyte adhesion deficiency, page 386)

Type I, II, III, IV, V and VI integral proteins (Figure 11-14)

Important Concepts

What type of linkages/interactions hold proteins on membranes?

Secondary structure

What is the most common structural motif in membrane spanning proteins? What is the second most common? Can the hydropathy index be used to predict this second type of structure? 

What is a lipid raft?

What is a caveolin?

Describe four examples of membrane fusion.

What are SNAREs and SNAPs?

How does the HA protein allow the flu virus DNA into a host cell?

Transport across membranes I: Passive Transport, no energy required

Words that you should be able to define:

simple diffusion

selectively permeable

facilitated diffusion

membrane potential (either chemical or electrical)\

osmosis 

transporters

permeases

aquaporins

Important concepts: 

Why are the structures of many transporters not known?

What contributes to the thermodynamic barriers that impede membrane transport?

What driving forces allow passive diffusion to occur with transporters?

How are transporters analogous to enzymes?

How do tranporters differ from enzymes?

Give examples of locations of aquaporins.

How do aquaporins work? How is their proposed structure related to their function?

Where is the GluT1 glucose transporter found? How is the proposed structure of this transporter related to its function? How is it specific for glucose?

Michalis-Menton kinetics can be applied to transporters!

What is the value of Kt for D-glucose? For galactose? For L-glucose? What does Kt mean?

Comparison of Erythrocytes and Hepatocytes

The liver has GluT2 transporters and they have a Kt value of 66 mM. If blood glucose levels were 5 mM, which tissue would take up glucose? Make a graph of velocity of glucose uptake vs glucose concentration. Aren't you impatient to learn about the glucose transporters in muscle and adipocytes?? See box 11-2!

One last type of energy free (passive) transporters: Cotransport systems.

Look at figure 11-33 to see how the chloride-bicarbonate exchanger works to shuttle CO2 out of the tissues, into the blood as bicarbonate and then out of the lungs.


 Membrane Transport II: Active diffusion (Energy required!)