Title: Announcements, Feb. 9
1Announcements, Feb. 9
- Reading for today 154-171 on membrane lipids.
- Reading for Monday 172-186 on membrane proteins.
- Reading for Wednesday 191-207 on membrane
transport. - Reading for Friday 207-216 on energetics of
membrane transport.
2Outline/Learning Objectives
- I. Membrane lipids
- Membrane functions
- Isolating membrane lipids
- Historical models of membranes
- Fluid mosaic model
- Evidence concerning lipid part of membrane
- After reading the text, attending lecture, and
reviewing lecture notes, you should be able to - List various functions of membranes.
- Explain how thin-layer chromatography (TLC) can
be used to fractionate lipids. - Compare historical models of membrane structure.
- Describe experimental evidence for membrane lipid
composition, structure and fluidity.
3Membrane Functions
4Membranes How would you study them?
5MB phospholipids
Note backbone is glycerol
Note back- bone is serine
6Historical models of membrane structure
- Gorter and Grendel (1925)
- Estimated red cell surface area and extracted
lipid from "ghosts." - Predicted that area of RBC was 100 ?m2, found
that area covered by lipid was 200 ?m2 ,
indicating a bilayer - Davson and Danielli Model (1935)
- How does differential permeability come about?
- Proposed lipid bilayer protein lamellae on each
side (sandwich), pores allowed substances in or
out. - Robertson (1960)
- Viewed membranes with EM, seemed to agree with
Davson and Danielli model - Suggested that all membranes of the same
composition (unit membrane). - But unit MB model did not account for chemical
differences in membranes
7Fluid Mosaic Model Singer and Nicholson (1972)
Science 175720
81. Evidence of the phospholipid composition TLC
of various membranes
Conclusion
92. Evidence for Lipid BilayerX-ray
crystallography of Membranes
- X-ray crystallography of membranes directly
reveals the bilayer structure. - Polar head groups scatter electrons more at
peaks. - Distance between peaks is 10 nm.
10 nm
electron density
Data
distance
10Asymmetry and Movement of PLs
- Functional significance
- Contributes to net negative charge on inside
- PI is available for signaling function on inside.
- Glycolipids in outer leaflet, so CHO out.
- Inequality is maintained by movement properties
of phospholipids within the membrane - Rotation and lateral diffusion is rapid
- Transverse diffusion or "flip-flop" is rare,
mediated by protein translocases.
- Membrane asymmetry is generated during synthesis
in the ER - PC, SM mostly in outer leaflet
- PE, PS, PI mostly in inner leaflet
- Cholesterol 50 inner, 50 outer
113. Evidence for Lipid FluidityFluorescence
Recovery After Photobleaching (FRAP)
Lipids labeled
124. Evidence for FluidityDifferential Scanning
Calorimetry
- Measures uptake of heat during phase transitions
of lipids. - Below the transition temperature (Tm) lipids are
solid, above Tm lipids are fluid. - Saturated fatty acids have a higher Tm while
unsaturated fatty acids have a lower Tm (more
fluid). Why? - Double bonds make kinks in the tails, which
disrupt the crystal structure. - Longer fatty acid chains have a higher Tm while
shorter fatty acids have a lower Tm (more fluid).
Monoun- saturated
saturated
13Effects of Chain Length and Double Bonds on Tm
More fluid ?
Less fluid ?
14Effect of Unsaturated Fatty Acids on Fluidity
- CC in FA creates kinks in chain, so they pack
together less well. - Less able to form crystalline solid, therefore
stays liquid. - Organisms in cold environments increase the of
unsaturated FAs in their membranes.
15MB Fluidity Depends On
- Temperature
- Higher T, greater fluidity cells cant change.
- Unsaturated FAs
- Increase fluidity
- Length of FAs
- Shorter, more fluid
- Cholesterol
- Fluidity buffer
Cells can regulate
16Effect of Cholesterol on Fluidity
- Animal cells contain up to 50 cholesterol in
their membranes. - OH of cholesterol hydrogen bonds with O of ester
bonded fatty acid, while hydrocarbon rings
interact with hydrophobic hydrocarbon chains of
fatty acids
Acts as a fluidity buffer Makes MB less fluid at
higher temperatures than without cholesterol,
since FAs immobilized Makes MB more fluid at
lower temperatures than without cholesterol,
since it disrupts packing into a crystal.
17Summary Evidence concerning the Lipid Portion of
the Membrane
- Estimated and measured surface area
- Membrane is a bilayer.
- Electron microscopy
- Trilaminar appearance of membranes.
- X-ray crystallography
- Membrane is a bilayer.
- Thin-layer chromatography
- Different membranes contain different
phospholipids. - Fluorescence recovery after photobleaching of
lipids - Membranes are fluid.
- Differential scanning calorimetry
- The phospholipid composition of membranes
determines how fluid they are.
18A recent twist on the Fluid Mosaic Model Lipid
rafts
Or Outside cell
- Small, specialized areas in membrane where some
lipids (primarily sphingolipids and cholesterol)
and proteins are concentrated. - Two monolayers move together thicker, less fluid
than normal membrane - Function signaling and/or transport of membrane
proteins?
19Visualization of Lipid Rafts
Atomic force microscopy reveals sphingomyelin
rafts (orange) protruding from a PC background
(black) in a mica-supported lipid bilayer.
Placental alkaline phosphatase (yellow peaks), a
GPI-anchored protein, is shown to be almost
exclusively raft-associated. For details see the
article by Saslowsky et al. J. Biol. Chem. 277,
Cover of 30, 2002.
20CHO modification of GlycolipidsThe ABO blood
groups
- Glycolipids partition into lipid rafts on
non-cytosolic side - Sugars added in lumen of Golgi, e.g. AB
antigens. - Recall the genetics
21ABO Blood Groups
A - A antigen only B - B antigen only AB -
Both A and B antigens O - Neither antigen