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Lipoprotein Membranes, Barriers and Gates

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Title: Lipoprotein Membranes, Barriers and Gates


1
Lipoprotein Membranes, Barriers and Gates
  • MSc Toxicology Cell Biology 2003

2
The common phospholipids
  • The membranes in and surrounding cells consists
    principally of phospholipids and proteins
  • Phospholipids are detergents and naturally
    orientate themselves as micelles or as bilayers
    depending on the shape of the lipid. This lipid
    bilayer is the basis of the membrane structure

3
Continued
  • The common phospolipids are based on glycerol.
    The 1 and 2 hydroxyls are esterified with fatty
    acids in the range C12 to C24 with C16 and C18
    being most common in warm blooded animals. A
    phosphate group is attached to the 3 position and
    to that may be attached either a choline, serine,
    ethanolamine or inositol residue.

4
Assymetry
  • Phospholipid bilayers separate distinct spaces
    (eg the cytosol and the outside world, the
    cytosol and a cell organelle etc.)
  • The two sides of a lipid bilayer may be quite
    different in lipid composition, for example in
    the plasma membrane the outer leaflet is
    primarily phosphatidyl choline, the inner leaflet
    phosphatidyl ethanolamine and serine
  • Flippases maintain the difference
  • And this is important. The presence of serine on
    the outer surface of the membrane signals that
    the cell is dying by apoptosis and should be
    removed.

5
And proteins
  • Proteins may associate with the lipid bilayer in
    a number of ways
  • They may bind to the surface of the bilayer on
    one side or the other.
  • They may pass through the bilayer and they may do
    so in either direction (remember a lipid bilayer
    is separating two distinct spaces eg cytosol and
    the lumen of the endoplasmic reticulum).
  • They may pass repeatedly through the membrane.
    This is seen especially with enzymes which are
    acting on hydrophobic molecules which will be
    dissolved in the bilayer

6
Continued
  • Other proteins are attached to the membrane in
    ways in which, in principle, they may readily be
    released. The two principle ways in which
    attachment concerns are-
  • Links with inositol residues either directly or
    via an short chain of carbohydrates
  • Links to hydrophobic molecules which act as
    membrane anchors. This is extremely important in
    the action of the small GTP binding proteins
    which play a major role in controlling cell
    function

7
Melting Membranes and fatty acid composition
  • The phospholipid bilayer may organise itself in
    two distinct ways.
  • At low temperatures the fatty acid side chains
    arrange themselves as a liquid crystal which
    will limit diffusion of proteins in the membrane
  • As the temperature is increased the membrane
    melts allowing free diffusion of the fatty
    acid.
  • The transition temperature between these forms
    is governed by the ease with which fatty acids
    pack. Long fatty acids and those with multiple
    double bonds pack poorly and have low transition
    temperature, useful for fish

8
Cholesterol
  • Steroids are the second most important lipid in
    the cell membranes. The concentration of
    cholesterol (the one used in animal cells) varies
    markedly between different membrane systems,
    being highest in the plasma membrane.
    Cholesterol thickens the membranes and smears
    the transition from liquid crystal to fluid mosaic

9
Sphingolipids and lipid rafts
  • While a part of the cholesterol is associated
    with the normal phospholipids another part is
    associated with the complex phospholipid
    sphingomyelin and forms rafts or microdomains
    which are especially concentrated in the plasma
    membrane. These lipid rafts seem to play a role
    in endo and exocytosis (eg HIV will only bud from
    a such a raft). They are both highly fashionable
    and poorly understood.

The figure shows a atomic force micrograph of
sphingomyelin rafts in a phosphlipid sea, The
yellow spikes are of a phosphtidyl
inositol-linked glycoprotrin
10
Other membrane lipids
  • The mitochondrial inner membrane is rich in
    cardiolipin which makes up about 20 if the
    membrane lipid.
  • Glycolipids are found only on thee outer surface
    of cells. In animals these largely are largely
    formed from sphingosine rather than from
    glycerol. Two major classes are the gangliosides
    and cerebrosides and, as these names indicate
    these are especially important in the central
    nervous system.

11
Passage across membranes
  • Hydrophobic molecules will dissolve in the
    membrane and move across the membrane readily.
    Binding proteins in the cytosol will extract
    them from the membranes
  • Fat soluble materials pass freely across
    membranes
  • Water passes freely across the membrane
  • Hydrophilic compounds pass very slowly across the
    membrane as illustrated by the difference in
    concentrations of Na and K ions between blood
    and cytosol. Transfer of such molecules requires
    permiases (only transport down a concentration or
    active transport (capable of transporting up a
    concentrationgradient

12
Assisted Passage
  • The simplest way in which molecules can move
    across membranes is as a result of the action of
    permeases. These bind the material to be
    carried, flip in the membrane and release on the
    other side. They can only transport down a
    concentration gradient but if the compound is
    removed readily once in the cell (eg glucose is
    converted to glucose-6-phosphate) then there will
    be net movement
  • Related are exchange transporters. These are
    especially important in mitochondria where they
    mediate exchange of ADP for ATP and carry di and
    tricarboxylate acids

13
Transfer up concentration gradients
  • This requires energy. This may be supplied by
  • By ATP directly. Examples here are transfer of
    Na and K across the plasma membrane. This
    carrier is especially interesting in that three
    positively charged ions are moved out of the cell
    for every two pumped in. The result is to set up
    a potential gradient across the plasma membrane.
    Other important pumps are the H ion pump that
    acidifies the endosomal compartment and lowers
    the pH in the stomach and the Ca ion pump in
    the e.r.

14
Continued
  • 2) A second type of transfer up a concentration
    gradient is co-transportation. Here passage of
    one molecule up its concentration gradient is
    balanced by passage of another molecule down its
    gradient. Thus glucose is absorbed in the
    intestine by a co-transporter in which Na ions
    pass into the cell along with the glucose. The
    energy is provided indirectly by the Na/K pump.
    The glucose absorbed at the apical face is then
    released from the basolateral face by a permease

15
Movement of large molecules across membranes
  • Passage of proteins across membranes requires
    specific recognition the protein carries on it
    a ticket which specifies its final location.
  • The mechanisms will be described in later
    lectures when we discuss the cell organelles

16
Passage of messages across membranes
  • Peptide hormones and growth factors act by
    binding to receptors on the cell surface
  • The receptors are proteins which span the plasma
    membrane. The binding of a ligand to its
    receptor will cause a change in folding of the
    extracellular domaine of the receptor. This
    will, in turn result in changes both in the
    transmembrane domaine and then in the
    intracellular domaine.
  • The change in the intracellular domaine will
    activate enzyme activity, especially protein
    kinases, which will trigger a signal cascade
    within the cell

17
Membrane domains
  • We would expect that proteins should be able to
    diffuse freely in a membrane but in some cell
    types we find that they are restricted to
    particular areas. In some cases, such a
    epithelial cells the cells in a tissue are joined
    together by tight junctions in other cases such
    as spermatozoa and nerve axons the barrier is
    less clear

18
Membranes and plastic bags
  • Because lipid bilayers are impermeable to
    hydrophilic we tend to think that they must
    resemble something like cling film. This is not
    the case. We can use laser tweezers to move
    the membrane around. In addition if we look at a
    living cell we can see that membranes are
    continually breaking apart and rejoining the
    nearest analogy being an oil slick. However it
    should also be noted that, as we will see in the
    next lecture, the plasma membrane, in particular,
    is associated with filamentous elements which
    allows the cells to deform then spring back into
    shape

19
To Summarise
  • The core of the cell membranes is a phospholipid
    bilayer.
  • There are considerable differences between the
    concentrations of other lipids both within and
    between cells
  • Because the lipid bilayer is impermeable to
    hydrophilic materials special transport systems
    have evolved.
  • Because of the vital role of membranes and
    membrane-associated proteins in cell function
    agents which damage the membrane will usually
    show marked cytotoxicity
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