2-lipid.ppt

Lipids & Membranes
Copyright © 1999-2006 by Joyce J. Diwan.
All rights reserved.
Biochemistry of Metabolism

Lipids are non-polar (hydrophobic) compounds,
soluble in organic solvents.
Most membrane lipids are amphipathic, having a
non-polar end and a polar end.
Fatty acids consist of a hydrocarbon chain with a
carboxylic acid at one end.
A 16-C fatty acid: CH3(CH2)14-COO-
Non-polar polar
A 16-C fatty acid with one cis double bond between
C atoms 9-10 may be represented as 16:1 cis D9.

Some fatty acids and their common names:
14:0 myristic acid; 16:0 palmitic acid; 18:0 stearic acid;
18:1 cisD9 oleic acid
18:2 cisD9,12 linoleic acid
18:3 cisD9,12,15 a-linonenic acid
20:4 cisD5,8,11,14 arachidonic acid
20:5 cisD5,8,11,14,17 eicosapentaenoic acid (an omega-3)
Double bonds in fatty
acids usually have the
cis configuration.
Most naturally
occurring fatty acids
have an even number
of carbon atoms.
C
O
O
1
2
3
4
a


fatty acid with a cis-D9
double bond

There is free rotation about C-C bonds in the fatty acid
hydrocarbon, except where there is a double bond.
Each cis double bond causes a kink in the chain.
Rotation about other C-C bonds would permit a more
linear structure than shown, but there would be a kink.
C
O
O
1
2
3
4
a


fatty acid with a cis-D9
double bond

Glycerophospholipids
Glycerophospholipids
(phosphoglycerides), are common
constituents of cellular membranes.
They have a glycerol backbone.
Hydroxyls at C1 & C2 are esterified
to fatty acids.
C OH
H
CH2OH
CH2OH
glycerol
An ester forms
when a hydroxyl
reacts with a
carboxylic acid,
with loss of H2O.
Formation of an ester:
O O
R'OH + HO-C-R" R'-O-C-R'' + H2O

Phosphatidate
In phosphatidate:
 fatty acids are esterified to hydroxyls on C1 & C2
 the C3 hydroxyl is esterified to Pi.
O P O
O
O
H2C
CH
H2C
O
C
R1
O O C
O
R2
phosphatidate

In most glycerophospholipids (phosphoglycerides),
Pi is in turn esterified to OH of a polar head group (X):
e.g., serine, choline, ethanolamine, glycerol, or inositol.
The 2 fatty acids tend to be non-identical. They may differ
in length and/or the presence/absence of double bonds.
O P O
O
O
H2C
CH
H2C
O
C
R1
O O C
O
R2
X
glycerophospholipid

Phosphatidylinositol, with inositol as polar head group,
is one glycerophospholipid.
In addition to being a membrane lipid,
phosphatidylinositol has roles in cell signaling.
O P
O
O
H2C
CH
H2C
O
C
R1
O O C
O
R2
OH
H
OH
H
H
OH
H
OH
H
O
H OH
phosphatidyl-
inositol

Phosphatidylcholine, with choline as polar head
group, is another glycerophospholipid.
It is a common membrane lipid.
O P O
O
O
H2C
CH
H2C
O
C
R1
O O C
O
R2
CH2 CH2 N CH3
CH3
CH3
+
phosphatidylcholine

polar
non-polar
"kink" due to
double bond
O P O
O
O
H2C
CH
H2C
O
C
R1
O O C
O
R2
X
glycerophospholipid
Each glycerophospholipid
includes
 a polar region:
glycerol, carbonyl O
of fatty acids, Pi, & the
polar head group (X)
 non-polar hydrocarbon
tails of fatty acids (R1, R2).

Sphingosine may be reversibly
phosphorylated to produce the signal
molecule sphingosine-1-phosphate.
Other derivatives of sphingosine are
commonly found as constituents of
biological membranes.
H2C
H
C
OH
CH
N+ CH
C
CH2
CH3
H
H3
OH
( )12
sphingosine
Sphingolipids are derivatives of
the lipid sphingosine, which has a
long hydrocarbon tail, and a polar
domain that includes an amino group.
sphingosine-1-P
H2C
H
C
O
CH
N+
CH
C
CH2
CH3
H
H3
OH
( )12
P O
O

O

In the more complex sphingolipids,
a polar “head group" is esterified
to the terminal hydroxyl of the
sphingosine moiety of the ceramide.
H2C
H
C
OH
CH
N+ CH
C
CH2
CH3
H
H3
OH
( )12
sphingosine
H2C
H
C
OH
CH
NH CH
C
CH2
CH3
H
OH
( )12
C
R
O
ceramide
The amino group of sphingosine can
form an amide bond with a fatty acid
carboxyl, to yield a ceramide.

Sphingomyelin, with a phosphocholine head group, is
similar in size and shape to the glycerophospholipid
phosphatidyl choline.
Sphingomyelin has
a phosphocholine or
phosphethanolamine
head group.
Sphingomyelins are
common constituent
of plasma membranes
H2C
H
C
O
CH
NH CH
C
CH2
CH3
H
OH
( )12
C
R
O
P
O O
O
H2
C
H2
C
N
+
CH3
H3C
CH3
Sphingomyelin
phosphocholine
sphingosine
fatty acid


head group that is a complex oligosaccharide, including
the acidic sugar derivative sialic acid.
Cerebrosides and gangliosides, collectively called
glycosphingolipids, are commonly found in the outer
leaflet of the plasma membrane bilayer, with their sugar
chains extending out from the cell surface.
cerebroside with
-galactose head group
H2C
H
C CH
NH CH
C
CH2
CH3
OH
C
R
O
OH O
H H
H
OH
H
OH
CH2OH
H
O
H
( )12
A cerebroside is a
sphingolipid
(ceramide) with a
monosaccharide
such as glucose or
galactose as polar
head group.
A ganglioside is a
ceramide with a polar

Depending on the lipid, possible molecular arrangements:
 Various micelle structures. E.g., a spherical micelle is
a stable configuration for amphipathic lipids with a
conical shape, such as fatty acids.
 A bilayer. This is the most stable configuration for
amphipathic lipids with a cylindrical shape, such as
phospholipids.
Bilayer Spherical Micelle
Amphipathic lipids in
association with water form
complexes in which polar
regions are in contact with
water and hydrophobic
regions away from water.

liquid crystal crystal
In the liquid crystal state, hydrocarbon chains of
phospholipids are disordered and in constant motion.
At lower temperature, a membrane containing a single
phospholipid type undergoes transition to a crystalline
state in which fatty acid tails are fully extended, packing
is highly ordered, & van der Waals interactions between
adjacent chains are maximal.
Kinks in fatty acid chains, due to cis double bonds,
interfere with packing in the crystalline state, and lower
the phase transition temperature.
Membrane fluidity:
The interior of a lipid bilayer
is normally highly fluid.

Cholesterol is largely
hydrophobic.
But it has one polar group,
a hydroxyl, making it
amphipathic.
Cholesterol
HO
Cholesterol, an
important constituent
of cell membranes,
has a rigid ring
system and a short
branched
hydrocarbon tail.
cholesterol
PDB 1N83

Cholesterol
in membrane
Cholesterol inserts into bilayer membranes with its
hydroxyl group oriented toward the aqueous phase &
its hydrophobic ring system adjacent to fatty acid
chains of phospholipids.
The OH group of cholesterol forms hydrogen bonds
with polar phospholipid head groups.
Cholesterol
HO

But the presence of cholesterol in a phospholipid
membrane interferes with close packing of fatty acid
tails in the crystalline state, and thus inhibits transition
to the crystal state.
Phospholipid membranes with a high concentration of
cholesterol have a fluidity intermediate between the
liquid crystal and crystal states.
Cholesterol
in membrane
Interaction with the relatively rigid
cholesterol decreases the mobility of
hydrocarbon tails of phospholipids.

Two strategies by which phase changes of membrane
lipids are avoided:
 Cholesterol is abundant in membranes, such as
plasma membranes, that include many lipids with
long-chain saturated fatty acids.
In the absence of cholesterol, such membranes would
crystallize at physiological temperatures.
 The inner mitochondrial membrane lacks cholesterol,
but includes many phospholipids whose fatty acids
have one or more double bonds, which lower the
melting point to below physiological temperature.

High speed tracking of individual lipid molecules has
shown that lateral movements are constrained within
small membrane domains.
Hopping from one domain to another occurs less
frequently than rapid movements within a domain.
The apparent constraints on lateral movements of lipids
(and proteins) has been attributed to integral membrane
proteins, anchored to the cytoskeleton, functioning as a
picket fence. See the website of the Kusumi laboratory.
Lateral Mobility
Lateral mobility of a lipid,
within the plane of a
membrane, is depicted at
right and in an animation.

Flip-flop would require the polar head-group of a lipid to
traverse the hydrophobic core of the membrane.
The two leaflets of a bilayer membrane tend to differ in
their lipid composition.
Flippases catalyze flip-flop in membranes where lipid
synthesis occurs.
Some membranes contain enzymes that actively transport
particular lipids from one monolayer to the other.
Flip Flop
Flip-flop of lipids (from one
half of a bilayer to the other)
is normally very slow.

Peripheral proteins are on the membrane surface.
They are water-soluble, with mostly hydrophilic surfaces.
Often peripheral proteins can be dislodged by conditions
that disrupt ionic & H-bond interactions, e.g., extraction
with solutions containing high concentrations of salts,
change of pH, and/or chelators that bind divalent cations.
Membrane
proteins may be
classified as:
 peripheral
 integral
 having a
lipid anchor integral
lipid
anchor
peripheral
lipid bilayer
Membrane
Proteins

Many proteins have a modular design, with different
segments of the primary structure folding into domains
with different functions.
Some cytosolic proteins have domains that bind to polar
head groups of lipids that transiently exist in a membrane.
The enzymes that create or degrade these lipids are subject
to signal-mediated regulation, providing a mechanism for
modulating affinity of a protein for a membrane surface.
regulatory catalytic membrane
domain domain binding
hypothetical protein

O P
O
O
H2C
CH
H2C
O
C
R1
O O C
O
R2
OH
H
OPO3
2
H
H
OPO3
2
H
OH
H
O
H OH
1 6
5
4
3
2
PIP2
phosphatidylinositol-
4,5-bisphosphate
E.g., pleckstrin homology (PH) domains bind to
phosphorylated derivatives of phosphatidylinositol.
Some PH domains bind PIP2 (PI-4,5-P2).

Other pleckstrin homology domains recognize and bind
phosphatidylinositol derivatives with Pi esterified at the
3' OH of inositol. E.g., PI-3-P, PI-3,4-P2, PI-3,4,5-P3.
O P
O
O
H2C
CH
H2C
O
C
R1
O O C
O
R2
OH
H
OH
H
H
OH
H
OPO3
2
H
O
H OH
1 6
5
2
3 4
phosphatidyl-
inositol-
3-phosphate

Some proteins bind to membranes via a covalently
attached lipid anchor, that inserts into the bilayer.
A protein may link to the cytosolic surface of the plasma
membrane via a covalently attached fatty acid (e.g.,
palmitate or myristate) or an isoprenoid group.
Palmitate is usually attached via an ester linkage to the
thiol of a cysteine residue.
A protein may be released from plasma membrane to
cytosol via depalmitoylation, hydrolysis of the ester link.
lipid
anchor
membrane
H3C (CH2)14 C
O
S CH2 CH
C
NH
O
palmitate
cysteine
residue

An isoprenoid such as a farnesyl
residue, is attached to some proteins
via a thioether linkage to a cysteine thiol.
CH CH2
C
H3C
CH3
CH CH2
C
CH2
CH3
CH CH2 S Protein
C
CH2
CH3
farnesyl residue linked to protein via cysteine S
lipid
anchor
membrane

Glycosylphosphatidylinositols (GPI) are complex
glycolipids that attach some proteins to the outer surface
of the plasma membrane.
The linkage is similar to the following, although the
oligosaccharide composition may vary:
protein (C-term.) - phosphoethanolamine – mannose - mannose -
mannose - N-acetylglucosamine – inositol (of PI in membrane)
The protein is tethered some distance out from the
membrane surface by the long oligosaccharide chain.
GPI-linked proteins may be released from the outer
cell surface by phospholipases.

Integral proteins have domains that extend into the
hydrocarbon core of the membrane.
Often they span the bilayer.
Intramembrane domains have largely hydrophobic
surfaces, that interact with membrane lipids.
integral
lipid
anchor
peripheral
lipid bilayer
Membrane
Proteins

 Hydrophobic domains of detergents substitute for
lipids, coating hydrophobic surfaces of integral proteins.
 Polar domains of detergents interact with water.
If detergents are removed, purified integral proteins tend
to aggregate & come out of solution. Their hydrophobic
surfaces associate to minimize contact with water.
Amphipathic
detergents are
required for
solubilization of
integral proteins
from membranes.
detergent
solubilization
Protein with
bound detergent
polar
non-polar
membrane

Lipid rafts:
 Complex sphingolipids tend to separate out from
glycerophospholipids & co-localize with cholesterol in
membrane microdomains called lipid rafts.
 Membrane fragments assumed to be lipid rafts are
found to be resistant to detergent solubilization,
which has facilitated their isolation & characterization.

 Differences in molecular shape may contribute to a
tendency for sphingolipids to separate out from
glycerophospholipids in membrane microdomains.
• Sphingolipids usually lack double bonds in their
fatty acid chains.
• Glycerophospholipids often include at least one
fatty acid that is kinked, due to one or more double
bonds.
• See diagram (in article by J. Santini & coworkers).
 Lipid raft domains tend to be thicker than adjacent
membrane areas, in part because the saturated
hydrocarbon chains of sphingolipids are more extended.

 Hydrogen bonding between the hydroxyl group of
cholesterol and the amide group of sphingomyelin
may in part account for the observed affinity of
cholesterol for sphingomyelin in raft domains.
H2C
H
C
O
CH
NH CH
C
CH2
CH3
H
OH
( )12
C
R
O
P
O O
O
H2
C
H2
C
N
+
CH3
H3C
CH3
Sphingomyelin
phosphocholine
sphingosine
fatty acid

Cholesterol
HO

 Proteins involved in cell signaling often associate
with lipid raft domains.
• Otherwise soluble signal proteins often assemble in
complexes at the cytosolic surface of the plasma
membrane in part via insertion of attached fatty acyl
or isoprenoid lipid anchors into raft domains.
• Integral proteins may concentrate in raft domains via
interactions with raft lipids or with other raft proteins.
• Some raft domains contain derivatives of
phosphatidylinositol that bind signal proteins with
pleckstrin homology domains.

 Caveolin is a protein associated with the cytosolic leaflet
of the plasma membrane in caveolae.
Caveolin interacts with cholesterol and self-associates
as oligomers that may contribute to deforming the
membrane to create the unique morphology of caveolae.
Electron micrograph & information about caveolae
(home page of Deborah Brown at SUNY Stony Brook).
Diagram & information about lipid rafts
(website of Maciver lab at University of Edinburgh).
caveolae
cytosol
 Caveolae are invaginated lipid
raft domains of the plasma
membrane that have roles in cell
signaling and membrane
internalization.

A membrane-spanning a-helix is
the most common structural motif
found in integral proteins.
membrane
N
C
Integral protein structure
Atomic-resolution structures have been determined
for a small (but growing) number of integral membrane
proteins.
Integral proteins are difficult to crystallize for X-ray
analysis.
Because of their hydrophobic
transmembrane domains,
detergents must be present
during crystallization.

In an a-helix, amino acid R-groups protrude out from the
helically coiled polypeptide backbone.
The largely hydrophobic R-groups of a membrane-
spanning a-helix contact the hydrophobic membrane core,
while the more polar peptide backbone is buried.
Colors: C N O R-group (H atoms not shown).
a-helix
R-groups in magenta

Particular amino acids tend to occur at different
positions relative to the surface or interior of the bilayer
in transmembrane segments of integral proteins.
Residues with aliphatic side-chains (leucine, isoleucine,
alanine, valine) predominate in the middle of the bilayer.
H3N+
C COO
CH3
H
H3N+
C COO
CH CH3
CH2
CH3
H
H3N+
C COO
CH2
CH CH3
CH3
H
H3N+
C COO
CH CH3
CH3
H
alanine (Ala, A) isoleucine (Ile, I) leucine (Leu, L) valine (Val, V)
amino acids: non-polar aliphatic R-groups

It has been suggested that the polar character of the
tryptophan amide group and the tyrosine hydroxyl, along
with their hydrophobic ring structures, suit them for
localization at the polar/apolar interface.
tryptophan tyrosine
H2N C COO
CH2
HN
H
H3N+
C COO
CH2
OH
H
Tyrosine and
tryptophan are
common near the
membrane surface.

Lysine & arginine are often at the lipid/water interface,
with the positively charged groups at the ends of their
aliphatic side chains extending toward the polar
membrane surface.
H3N+
C COO
CH2
CH2
CH2
NH
C
NH2
NH2
H
H3N+
C COO
CH2
CH2
CH2
CH2
NH3
H


lysine arginine

Cytochrome oxidase is an integral protein whose intra-
membrane domains are mainly transmembrane a-helices.
Explore with Chime the a-helix colored green at far left.
membrane
Cytochrome oxidase dimer (PDB file 1OCC)

A 20-amino acid a-helix just spans a lipid bilayer.
Hydropathy plots are used to search for 20-amino
acid stretches of hydrophobic amino acids in the
primary sequence of a protein for which a crystal
structure is not available.
Putative hydrophobic transmembrane a-helices have
been identified this way in many membrane proteins.
Hydropathy plots alone are not conclusive.
Protein topology studies are used to test the
transmembrane distribution of protein domains
predicted by hydropathy plots.

 If a hydropathy plot indicates one 20-amino acid
hydrophobic stretch (1 putative transmembrane a-helix),
topology studies are expected to confirm location of
N & C termini on opposite sides of membrane.
 If two transmembrane a-helices are predicted, N & C
termini should be on the same side. The segment
between the a-helices should be on the other side.
N
C
membrane
N
C

Transmembrane topology is tested with impermeant
probes, added on one side of a membrane. For example:
 Protease enzymes. Degradation a protein segment
indicates exposure to the aqueous phase on the side of
the membrane to which a protease is added.
 Monoclonal antibodies raised to peptides equivalent
to individual segments of the protein. Binding
indicates surface exposure of a protein segment on the
side to which the Ab is added.
Such studies have shown that all copies of a given type of
integral protein have the same orientation relative to the
membrane. Flip-flop of integral proteins does not occur.

An a-helix lining a water-filled channel might have
polar amino acid R-groups facing the lumen, & non-polar
R-groups facing lipids or other hydrophobic a-helices.
Such mixed polarity would prevent detection by a
hydropathy plot.
A “helical
wheel” looks
down the axis
of an a-helix,
projecting side-
chains onto a
plane.
Simplified helical wheel diagram of four
a-helices lining the lumen of an ion channel.
Polar amino acid R-group
Non-polar amino acid R-group

Porin -barrel
While transmembrane a-
helices are the most common
structural motif for integral
proteins, a family of bacterial
outer envelope channel
proteins called porins have
instead  barrel structures.
A  barrel is a  sheet rolled
up to form a cylindrical pore.
At right is shown one channel
of a trimeric porin complex.
Porin Monomer
PDB 1AOS

In a -sheet, amino acid R-groups alternately point above
& below the sheet.
Much of porin primary structure consists of alternating
polar & non-polar amino acids.
• Polar residues face the aqueous lumen.
• Non-polar residues are in contact with membrane lipids.
Explore an example of a bacterial porin with Chime.
 polar R group,  non-polar R group

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