Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
PowerPoint®
Lecture Presentations for
Biology
Eighth Edition
Neil Campbell and Jane Reece
Lectures by Chris Romero, updated by Erin Barley with contributions from Joan Sharp
Chapter 7
Membrane Structure and
Function
Overview: Life at the Edge
• The plasma membrane is the boundary that
separates the living cell from its surroundings
• The plasma membrane exhibits selective
permeability, allowing some substances to
cross it more easily than others
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-1
Concept 7.1: Cellular membranes are fluid mosaics
of lipids and proteins
• Phospholipids are the most abundant lipid in
the plasma membrane
• Phospholipids are amphipathic molecules,
containing hydrophobic and hydrophilic regions
• The fluid mosaic model states that a
membrane is a fluid structure with a “mosaic” of
various proteins embedded in it
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Membrane Models: Scientific Inquiry
• Membranes have been chemically analyzed
and found to be made of proteins and lipids
• Scientists studying the plasma membrane
reasoned that it must be a phospholipid bilayer
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-2
Hydrophilic
head
WATER
Hydrophobic
tail
WATER
• In 1935, Hugh Davson and James Danielli
proposed a sandwich model in which the
phospholipid bilayer lies between two layers of
globular proteins
• Later studies found problems with this model,
particularly the placement of membrane proteins,
which have hydrophilic and hydrophobic regions
• In 1972, J. Singer and G. Nicolson proposed that
the membrane is a mosaic of proteins dispersed
within the bilayer, with only the hydrophilic regions
exposed to water
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-3
Phospholipid
bilayer
Hydrophobic regions
of protein
Hydrophilic
regions of protein
• Freeze-fracture studies of the plasma
membrane supported the fluid mosaic model
• Freeze-fracture is a specialized preparation
technique that splits a membrane along the
middle of the phospholipid bilayer
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-4
TECHNIQUE
Extracellular
layer
Knife
Proteins Inside of extracellular layer
RESULTS
Inside of cytoplasmic layer
Cytoplasmic layer
Plasma membrane
The Fluidity of Membranes
• Phospholipids in the plasma membrane can
move within the bilayer
• Most of the lipids, and some proteins, drift
laterally
• Rarely does a molecule flip-flop transversely
across the membrane
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-5
Lateral movement
(~107
times per second)
Flip-flop
(~ once per month)
(a) Movement of phospholipids
(b) Membrane fluidity
Fluid Viscous
Unsaturated hydrocarbon
tails with kinks
Saturated hydro-
carbon tails
(c) Cholesterol within the animal cell membrane
Cholesterol
Fig. 7-5a
(a) Movement of phospholipids
Lateral movement
(107
times per
second)
Flip-flop
( once per month)
Fig. 7-6
RESULTS
Membrane proteins
Mouse cell
Human cell
Hybrid cell
Mixed proteins
after 1 hour
• As temperatures cool, membranes switch from
a fluid state to a solid state
• The temperature at which a membrane
solidifies depends on the types of lipids
• Membranes rich in unsaturated fatty acids are
more fluid that those rich in saturated fatty
acids
• Membranes must be fluid to work properly;
they are usually about as fluid as salad oil
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-5b
(b) Membrane fluidity
Fluid
Unsaturated hydrocarbon
tails with kinks
Viscous
Saturated hydro-
carbon tails
• The steroid cholesterol has different effects on
membrane fluidity at different temperatures
• At warm temperatures (such as 37°C),
cholesterol restrains movement of
phospholipids
• At cool temperatures, it maintains fluidity by
preventing tight packing
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-5c
Cholesterol
(c) Cholesterol within the animal cell membrane
Membrane Proteins and Their Functions
• A membrane is a collage of different proteins
embedded in the fluid matrix of the lipid bilayer
• Proteins determine most of the membrane’s
specific functions
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-7
Fibers of
extracellular
matrix (ECM)
Glyco-
protein
Microfilaments
of cytoskeleton
Cholesterol
Peripheral
proteins
Integral
protein
CYTOPLASMIC SIDE
OF MEMBRANE
Glycolipid
EXTRACELLULAR
SIDE OF
MEMBRANE
Carbohydrate
• Peripheral proteins are bound to the surface
of the membrane
• Integral proteins penetrate the hydrophobic
core
• Integral proteins that span the membrane are
called transmembrane proteins
• The hydrophobic regions of an integral protein
consist of one or more stretches of nonpolar
amino acids, often coiled into alpha helices
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-8
N-terminus
C-terminus
 Helix
CYTOPLASMIC
SIDE
EXTRACELLULAR
SIDE
• Six major functions of membrane proteins:
– Transport
– Enzymatic activity
– Signal transduction
– Cell-cell recognition
– Intercellular joining
– Attachment to the cytoskeleton and
extracellular matrix (ECM)
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-9
(a) Transport
ATP
(b) Enzymatic activity
Enzymes
(c) Signal transduction
Signal transduction
Signaling molecule
Receptor
(d) Cell-cell recognition
Glyco-
protein
(e) Intercellular joining (f) Attachment to
the cytoskeleton
and extracellular
matrix (ECM)
Fig. 7-9ac
(a) Transport (b) Enzymatic activity (c) Signal transduction
ATP
Enzymes
Signal transduction
Signaling molecule
Receptor
Fig. 7-9df
(d) Cell-cell recognition
Glyco-
protein
(e) Intercellular joining (f) Attachment to
the cytoskeleton
and extracellular
matrix (ECM)
The Role of Membrane Carbohydrates in Cell-Cell
Recognition
• Cells recognize each other by binding to
surface molecules, often carbohydrates, on the
plasma membrane
• Membrane carbohydrates may be covalently
bonded to lipids (forming glycolipids) or more
commonly to proteins (forming glycoproteins)
• Carbohydrates on the external side of the
plasma membrane vary among species,
individuals, and even cell types in an individual
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Synthesis and Sidedness of Membranes
• Membranes have distinct inside and outside
faces
• The asymmetrical distribution of proteins,
lipids, and associated carbohydrates in the
plasma membrane is determined when the
membrane is built by the ER and Golgi
apparatus
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-10
ER
1
Transmembrane
glycoproteins
Secretory
protein
Glycolipid
2
Golgi
apparatus
Vesicle
3
4
Secreted
protein
Transmembrane
glycoprotein
Plasma membrane:
Cytoplasmic face
Extracellular face
Membrane glycolipid
Concept 7.2: Membrane structure results in
selective permeability
• A cell must exchange materials with its
surroundings, a process controlled by the
plasma membrane
• Plasma membranes are selectively permeable,
regulating the cell’s molecular traffic
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
The Permeability of the Lipid Bilayer
• Hydrophobic (nonpolar) molecules, such as
hydrocarbons, can dissolve in the lipid bilayer
and pass through the membrane rapidly
• Polar molecules, such as sugars, do not cross
the membrane easily
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Transport Proteins
• Transport proteins allow passage of
hydrophilic substances across the membrane
• Some transport proteins, called channel
proteins, have a hydrophilic channel that
certain molecules or ions can use as a tunnel
• Channel proteins called aquaporins facilitate
the passage of water
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
• Other transport proteins, called carrier proteins,
bind to molecules and change shape to shuttle
them across the membrane
• A transport protein is specific for the substance
it moves
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Concept 7.3: Passive transport is diffusion of a
substance across a membrane with no energy
investment
• Diffusion is the tendency for molecules to
spread out evenly into the available space
• Although each molecule moves randomly,
diffusion of a population of molecules may
exhibit a net movement in one direction
• At dynamic equilibrium, as many molecules
cross one way as cross in the other direction
Animation: Membrane Selectivity
Animation: Membrane Selectivity Animation: Diffusion
Animation: Diffusion
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-11
Molecules of dye Membrane (cross section)
WATER
Net diffusion Net diffusion Equilibrium
(a) Diffusion of one solute
Net diffusion
Net diffusion
Net diffusion
Net diffusion
Equilibrium
Equilibrium
(b) Diffusion of two solutes
Molecules of dye
Fig. 7-11a
Membrane (cross section)
WATER
Net diffusion Net diffusion
(a) Diffusion of one solute
Equilibrium
• Substances diffuse down their concentration
gradient, the difference in concentration of a
substance from one area to another
• No work must be done to move substances
down the concentration gradient
• The diffusion of a substance across a biological
membrane is passive transport because it
requires no energy from the cell to make it
happen
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
(b) Diffusion of two solutes
Fig. 7-11b
Net diffusion
Net diffusion
Net diffusion
Net diffusion
Equilibrium
Equilibrium
Effects of Osmosis on Water Balance
• Osmosis is the diffusion of water across a
selectively permeable membrane
• Water diffuses across a membrane from the
region of lower solute concentration to the
region of higher solute concentration
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Lower
concentration
of solute (sugar)
Fig. 7-12
H2O
Higher
concentration
of sugar
Selectively
permeable
membrane
Same concentration
of sugar
Osmosis
Water Balance of Cells Without Walls
• Tonicity is the ability of a solution to cause a
cell to gain or lose water
• Isotonic solution: Solute concentration is the
same as that inside the cell; no net water
movement across the plasma membrane
• Hypertonic solution: Solute concentration is
greater than that inside the cell; cell loses
water
• Hypotonic solution: Solute concentration is
less than that inside the cell; cell gains water
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-13
Hypotonic solution
(a) Animal
cell
(b) Plant
cell
H2O
Lysed
H2O
Turgid (normal)
H2O
H2O
H2O
H2O
Normal
Isotonic solution
Flaccid
H2O
H2O
Shriveled
Plasmolyzed
Hypertonic solution
• Hypertonic or hypotonic environments create
osmotic problems for organisms
• Osmoregulation, the control of water balance,
is a necessary adaptation for life in such
environments
• The protist Paramecium, which is hypertonic to
its pond water environment, has a contractile
vacuole that acts as a pump
Video:
Video: Chlamydomonas
Chlamydomonas Video:
Video: Paramecium
Paramecium Vacuole
Vacuole
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-14
Filling vacuole 50 µm
(a) A contractile vacuole fills with fluid that enters from
a system of canals radiating throughout the cytoplasm.
Contracting vacuole
(b) When full, the vacuole and canals contract, expelling
fluid from the cell.
Water Balance of Cells with Walls
• Cell walls help maintain water balance
• A plant cell in a hypotonic solution swells until
the wall opposes uptake; the cell is now turgid
(firm)
• If a plant cell and its surroundings are isotonic,
there is no net movement of water into the cell;
the cell becomes flaccid (limp), and the plant
may wilt
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Video: Plasmolysis
Video: Plasmolysis
Video: Turgid
Video: Turgid Elodea
Elodea
Animation: Osmosis
Animation: Osmosis
• In a hypertonic environment, plant cells lose
water; eventually, the membrane pulls away
from the wall, a usually lethal effect called
plasmolysis
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Facilitated Diffusion: Passive Transport Aided by
Proteins
• In facilitated diffusion, transport proteins
speed the passive movement of molecules
across the plasma membrane
• Channel proteins provide corridors that allow a
specific molecule or ion to cross the membrane
• Channel proteins include
– Aquaporins, for facilitated diffusion of water
– Ion channels that open or close in response
to a stimulus (gated channels)
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-15
EXTRACELLULAR
FLUID
Channel protein
(a) A channel protein
Solute
CYTOPLASM
Solute
Carrier protein
(b) A carrier protein
• Carrier proteins undergo a subtle change in
shape that translocates the solute-binding site
across the membrane
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
• Some diseases are caused by malfunctions in
specific transport systems, for example the
kidney disease cystinuria
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Concept 7.4: Active transport uses energy to move
solutes against their gradients
• Facilitated diffusion is still passive because the
solute moves down its concentration gradient
• Some transport proteins, however, can move
solutes against their concentration gradients
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
The Need for Energy in Active Transport
• Active transport moves substances against
their concentration gradient
• Active transport requires energy, usually in the
form of ATP
• Active transport is performed by specific
proteins embedded in the membranes
Animation: Active Transport
Animation: Active Transport
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
• Active transport allows cells to maintain
concentration gradients that differ from their
surroundings
• The sodium-potassium pump is one type of
active transport system
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-16-1
EXTRACELLULAR
FLUID
[Na+
] high
[K+
] low
Na+
Na+
Na+
[Na+
] low
[K+
] high
CYTOPLASM
Cytoplasmic Na+
binds to
the sodium-potassium pump.
1
Na+
binding stimulates
phosphorylation by ATP.
Fig. 7-16-2
Na+
Na+
Na+
ATP
P
ADP
2
Fig. 7-16-3
Phosphorylation causes
the protein to change its
shape. Na+
is expelled to
the outside.
Na+
P
Na+
Na+
3
Fig. 7-16-4
K+
binds on the
extracellular side and
triggers release of the
phosphate group.
P
P
K+
K+
4
Fig. 7-16-5
Loss of the phosphate
restores the protein’s original
shape.
K+
K+
5
Fig. 7-16-6
K+
is released, and the
cycle repeats.
K+
K+
6
2
EXTRACELLULAR
FLUID
[Na+
] high
[K+
] low
[Na+
] low
[K+
] high
Na+
Na+
Na+
Na+
Na+
Na+
CYTOPLASM
ATP
ADP
P
Na+
Na+
Na+
P
3
K+
K+
6
K+
K+
5 4
K+
K+
P
P
1
Fig. 7-16-7
Fig. 7-17
Passive transport
Diffusion Facilitated diffusion
Active transport
AT
P
How Ion Pumps Maintain Membrane Potential
• Membrane potential is the voltage difference
across a membrane
• Voltage is created by differences in the
distribution of positive and negative ions
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
• Two combined forces, collectively called the
electrochemical gradient, drive the diffusion
of ions across a membrane:
– A chemical force (the ion’s concentration
gradient)
– An electrical force (the effect of the membrane
potential on the ion’s movement)
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
• An electrogenic pump is a transport protein
that generates voltage across a membrane
• The sodium-potassium pump is the major
electrogenic pump of animal cells
• The main electrogenic pump of plants, fungi,
and bacteria is a proton pump
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-18
EXTRACELLULAR
FLUID
H+
H+
H+
H+
Proton pump
+
+
+
H+
H+
+
+
H+
–
–
–
–
ATP
CYTOPLASM
–
Cotransport: Coupled Transport by a Membrane
Protein
• Cotransport occurs when active transport of a
solute indirectly drives transport of another
solute
• Plants commonly use the gradient of hydrogen
ions generated by proton pumps to drive active
transport of nutrients into the cell
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-19
Proton pump
–
–
–
–
–
–
+
+
+
+
+
+
ATP
H+
H+
H+
H+
H+
H+
H+
H+
Diffusion
of H+
Sucrose-H+
cotransporter
Sucrose
Sucrose
Concept 7.5: Bulk transport across the plasma
membrane occurs by exocytosis and endocytosis
• Small molecules and water enter or leave the
cell through the lipid bilayer or by transport
proteins
• Large molecules, such as polysaccharides and
proteins, cross the membrane in bulk via
vesicles
• Bulk transport requires energy
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Exocytosis
• In exocytosis, transport vesicles migrate to the
membrane, fuse with it, and release their
contents
• Many secretory cells use exocytosis to export
their products
Animation: Exocytosis
Animation: Exocytosis
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Endocytosis
• In endocytosis, the cell takes in macromolecules
by forming vesicles from the plasma membrane
• Endocytosis is a reversal of exocytosis, involving
different proteins
• There are three types of endocytosis:
– Phagocytosis (“cellular eating”)
– Pinocytosis (“cellular drinking”)
– Receptor-mediated endocytosis
Animation: Exocytosis and Endocytosis Introduction
Animation: Exocytosis and Endocytosis Introduction
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
• In phagocytosis a cell engulfs a particle in a
vacuole
• The vacuole fuses with a lysosome to digest
the particle
Animation: Phagocytosis
Animation: Phagocytosis
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-20
PHAGOCYTOSIS
EXTRACELLULAR
FLUID
CYTOPLASM
Pseudopodium
“Food”or
other particle
Food
vacuole
PINOCYTOSIS
1 µm
Pseudopodium
of amoeba
Bacterium
Food vacuole
An amoeba engulfing a bacterium
via phagocytosis (TEM)
Plasma
membrane
Vesicle
0.5 µm
Pinocytosis vesicles
forming (arrows) in
a cell lining a small
blood vessel (TEM)
RECEPTOR-MEDIATED ENDOCYTOSIS
Receptor
Coat protein
Coated
vesicle
Coated
pit
Ligand
Coat
protein
Plasma
membrane
A coated pit
and a coated
vesicle formed
during
receptor-
mediated
endocytosis
(TEMs)
0.25 µm
Fig. 7-20a
PHAGOCYTOSIS
CYTOPLASM
EXTRACELLULAR
FLUID
Pseudopodium
“Food” or
other particle
Food
vacuole Food vacuole
Bacterium
An amoeba engulfing a bacterium
via phagocytosis (TEM)
Pseudopodium
of amoeba
1 µm
• In pinocytosis, molecules are taken up when
extracellular fluid is “gulped” into tiny vesicles
Animation: Pinocytosis
Animation: Pinocytosis
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-20b
PINOCYTOSIS
Plasma
membrane
Vesicle
0.5 µm
Pinocytosis vesicles
forming (arrows) in
a cell lining a small
blood vessel (TEM)
• In receptor-mediated endocytosis, binding of
ligands to receptors triggers vesicle formation
• A ligand is any molecule that binds specifically
to a receptor site of another molecule
Animation: Receptor-Mediated Endocytosis
Animation: Receptor-Mediated Endocytosis
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
Fig. 7-20c
RECEPTOR-MEDIATED ENDOCYTOSIS
Receptor
Coat protein
Coated
pit
Ligand
Coat
protein
Plasma
membrane
0.25 µm
Coated
vesicle
A coated pit
and a coated
vesicle formed
during
receptor-
mediated
endocytosis
(TEMs)
Fig. 7-UN1
Passive transport:
Facilitated diffusion
Channel
protein
Carrier
protein
Fig. 7-UN2
Active transport:
ATP
Fig. 7-UN3
Environment:
0.01 M sucrose
0.01 M glucose
0.01 M fructose
“Cell”
0.03 M sucrose
0.02 M glucose
Fig. 7-UN4
You should now be able to:
1. Define the following terms: amphipathic
molecules, aquaporins, diffusion
2. Explain how membrane fluidity is influenced
by temperature and membrane composition
3. Distinguish between the following pairs or
sets of terms: peripheral and integral
membrane proteins; channel and carrier
proteins; osmosis, facilitated diffusion, and
active transport; hypertonic, hypotonic, and
isotonic solutions
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
4. Explain how transport proteins facilitate
diffusion
5. Explain how an electrogenic pump creates
voltage across a membrane, and name two
electrogenic pumps
6. Explain how large molecules are transported
across a cell membrane
Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Membrane Structure and Function campbell

  • 1.
    Copyright © 2008Pearson Education, Inc., publishing as Pearson Benjamin Cummings PowerPoint® Lecture Presentations for Biology Eighth Edition Neil Campbell and Jane Reece Lectures by Chris Romero, updated by Erin Barley with contributions from Joan Sharp Chapter 7 Membrane Structure and Function
  • 2.
    Overview: Life atthe Edge • The plasma membrane is the boundary that separates the living cell from its surroundings • The plasma membrane exhibits selective permeability, allowing some substances to cross it more easily than others Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 3.
  • 4.
    Concept 7.1: Cellularmembranes are fluid mosaics of lipids and proteins • Phospholipids are the most abundant lipid in the plasma membrane • Phospholipids are amphipathic molecules, containing hydrophobic and hydrophilic regions • The fluid mosaic model states that a membrane is a fluid structure with a “mosaic” of various proteins embedded in it Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 5.
    Membrane Models: ScientificInquiry • Membranes have been chemically analyzed and found to be made of proteins and lipids • Scientists studying the plasma membrane reasoned that it must be a phospholipid bilayer Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 6.
  • 7.
    • In 1935,Hugh Davson and James Danielli proposed a sandwich model in which the phospholipid bilayer lies between two layers of globular proteins • Later studies found problems with this model, particularly the placement of membrane proteins, which have hydrophilic and hydrophobic regions • In 1972, J. Singer and G. Nicolson proposed that the membrane is a mosaic of proteins dispersed within the bilayer, with only the hydrophilic regions exposed to water Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 8.
    Fig. 7-3 Phospholipid bilayer Hydrophobic regions ofprotein Hydrophilic regions of protein
  • 9.
    • Freeze-fracture studiesof the plasma membrane supported the fluid mosaic model • Freeze-fracture is a specialized preparation technique that splits a membrane along the middle of the phospholipid bilayer Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 10.
    Fig. 7-4 TECHNIQUE Extracellular layer Knife Proteins Insideof extracellular layer RESULTS Inside of cytoplasmic layer Cytoplasmic layer Plasma membrane
  • 11.
    The Fluidity ofMembranes • Phospholipids in the plasma membrane can move within the bilayer • Most of the lipids, and some proteins, drift laterally • Rarely does a molecule flip-flop transversely across the membrane Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 12.
    Fig. 7-5 Lateral movement (~107 timesper second) Flip-flop (~ once per month) (a) Movement of phospholipids (b) Membrane fluidity Fluid Viscous Unsaturated hydrocarbon tails with kinks Saturated hydro- carbon tails (c) Cholesterol within the animal cell membrane Cholesterol
  • 13.
    Fig. 7-5a (a) Movementof phospholipids Lateral movement (107 times per second) Flip-flop ( once per month)
  • 14.
    Fig. 7-6 RESULTS Membrane proteins Mousecell Human cell Hybrid cell Mixed proteins after 1 hour
  • 15.
    • As temperaturescool, membranes switch from a fluid state to a solid state • The temperature at which a membrane solidifies depends on the types of lipids • Membranes rich in unsaturated fatty acids are more fluid that those rich in saturated fatty acids • Membranes must be fluid to work properly; they are usually about as fluid as salad oil Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 16.
    Fig. 7-5b (b) Membranefluidity Fluid Unsaturated hydrocarbon tails with kinks Viscous Saturated hydro- carbon tails
  • 17.
    • The steroidcholesterol has different effects on membrane fluidity at different temperatures • At warm temperatures (such as 37°C), cholesterol restrains movement of phospholipids • At cool temperatures, it maintains fluidity by preventing tight packing Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 18.
    Fig. 7-5c Cholesterol (c) Cholesterolwithin the animal cell membrane
  • 19.
    Membrane Proteins andTheir Functions • A membrane is a collage of different proteins embedded in the fluid matrix of the lipid bilayer • Proteins determine most of the membrane’s specific functions Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 20.
    Fig. 7-7 Fibers of extracellular matrix(ECM) Glyco- protein Microfilaments of cytoskeleton Cholesterol Peripheral proteins Integral protein CYTOPLASMIC SIDE OF MEMBRANE Glycolipid EXTRACELLULAR SIDE OF MEMBRANE Carbohydrate
  • 21.
    • Peripheral proteinsare bound to the surface of the membrane • Integral proteins penetrate the hydrophobic core • Integral proteins that span the membrane are called transmembrane proteins • The hydrophobic regions of an integral protein consist of one or more stretches of nonpolar amino acids, often coiled into alpha helices Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 22.
  • 23.
    • Six majorfunctions of membrane proteins: – Transport – Enzymatic activity – Signal transduction – Cell-cell recognition – Intercellular joining – Attachment to the cytoskeleton and extracellular matrix (ECM) Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 24.
    Fig. 7-9 (a) Transport ATP (b)Enzymatic activity Enzymes (c) Signal transduction Signal transduction Signaling molecule Receptor (d) Cell-cell recognition Glyco- protein (e) Intercellular joining (f) Attachment to the cytoskeleton and extracellular matrix (ECM)
  • 25.
    Fig. 7-9ac (a) Transport(b) Enzymatic activity (c) Signal transduction ATP Enzymes Signal transduction Signaling molecule Receptor
  • 26.
    Fig. 7-9df (d) Cell-cellrecognition Glyco- protein (e) Intercellular joining (f) Attachment to the cytoskeleton and extracellular matrix (ECM)
  • 27.
    The Role ofMembrane Carbohydrates in Cell-Cell Recognition • Cells recognize each other by binding to surface molecules, often carbohydrates, on the plasma membrane • Membrane carbohydrates may be covalently bonded to lipids (forming glycolipids) or more commonly to proteins (forming glycoproteins) • Carbohydrates on the external side of the plasma membrane vary among species, individuals, and even cell types in an individual Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 28.
    Synthesis and Sidednessof Membranes • Membranes have distinct inside and outside faces • The asymmetrical distribution of proteins, lipids, and associated carbohydrates in the plasma membrane is determined when the membrane is built by the ER and Golgi apparatus Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 29.
  • 30.
    Concept 7.2: Membranestructure results in selective permeability • A cell must exchange materials with its surroundings, a process controlled by the plasma membrane • Plasma membranes are selectively permeable, regulating the cell’s molecular traffic Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 31.
    The Permeability ofthe Lipid Bilayer • Hydrophobic (nonpolar) molecules, such as hydrocarbons, can dissolve in the lipid bilayer and pass through the membrane rapidly • Polar molecules, such as sugars, do not cross the membrane easily Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 32.
    Transport Proteins • Transportproteins allow passage of hydrophilic substances across the membrane • Some transport proteins, called channel proteins, have a hydrophilic channel that certain molecules or ions can use as a tunnel • Channel proteins called aquaporins facilitate the passage of water Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 33.
    • Other transportproteins, called carrier proteins, bind to molecules and change shape to shuttle them across the membrane • A transport protein is specific for the substance it moves Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 34.
    Concept 7.3: Passivetransport is diffusion of a substance across a membrane with no energy investment • Diffusion is the tendency for molecules to spread out evenly into the available space • Although each molecule moves randomly, diffusion of a population of molecules may exhibit a net movement in one direction • At dynamic equilibrium, as many molecules cross one way as cross in the other direction Animation: Membrane Selectivity Animation: Membrane Selectivity Animation: Diffusion Animation: Diffusion Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 35.
    Fig. 7-11 Molecules ofdye Membrane (cross section) WATER Net diffusion Net diffusion Equilibrium (a) Diffusion of one solute Net diffusion Net diffusion Net diffusion Net diffusion Equilibrium Equilibrium (b) Diffusion of two solutes
  • 36.
    Molecules of dye Fig.7-11a Membrane (cross section) WATER Net diffusion Net diffusion (a) Diffusion of one solute Equilibrium
  • 37.
    • Substances diffusedown their concentration gradient, the difference in concentration of a substance from one area to another • No work must be done to move substances down the concentration gradient • The diffusion of a substance across a biological membrane is passive transport because it requires no energy from the cell to make it happen Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 38.
    (b) Diffusion oftwo solutes Fig. 7-11b Net diffusion Net diffusion Net diffusion Net diffusion Equilibrium Equilibrium
  • 39.
    Effects of Osmosison Water Balance • Osmosis is the diffusion of water across a selectively permeable membrane • Water diffuses across a membrane from the region of lower solute concentration to the region of higher solute concentration Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 40.
    Lower concentration of solute (sugar) Fig.7-12 H2O Higher concentration of sugar Selectively permeable membrane Same concentration of sugar Osmosis
  • 41.
    Water Balance ofCells Without Walls • Tonicity is the ability of a solution to cause a cell to gain or lose water • Isotonic solution: Solute concentration is the same as that inside the cell; no net water movement across the plasma membrane • Hypertonic solution: Solute concentration is greater than that inside the cell; cell loses water • Hypotonic solution: Solute concentration is less than that inside the cell; cell gains water Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 42.
    Fig. 7-13 Hypotonic solution (a)Animal cell (b) Plant cell H2O Lysed H2O Turgid (normal) H2O H2O H2O H2O Normal Isotonic solution Flaccid H2O H2O Shriveled Plasmolyzed Hypertonic solution
  • 43.
    • Hypertonic orhypotonic environments create osmotic problems for organisms • Osmoregulation, the control of water balance, is a necessary adaptation for life in such environments • The protist Paramecium, which is hypertonic to its pond water environment, has a contractile vacuole that acts as a pump Video: Video: Chlamydomonas Chlamydomonas Video: Video: Paramecium Paramecium Vacuole Vacuole Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 44.
    Fig. 7-14 Filling vacuole50 µm (a) A contractile vacuole fills with fluid that enters from a system of canals radiating throughout the cytoplasm. Contracting vacuole (b) When full, the vacuole and canals contract, expelling fluid from the cell.
  • 45.
    Water Balance ofCells with Walls • Cell walls help maintain water balance • A plant cell in a hypotonic solution swells until the wall opposes uptake; the cell is now turgid (firm) • If a plant cell and its surroundings are isotonic, there is no net movement of water into the cell; the cell becomes flaccid (limp), and the plant may wilt Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 46.
    Video: Plasmolysis Video: Plasmolysis Video:Turgid Video: Turgid Elodea Elodea Animation: Osmosis Animation: Osmosis • In a hypertonic environment, plant cells lose water; eventually, the membrane pulls away from the wall, a usually lethal effect called plasmolysis Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 47.
    Facilitated Diffusion: PassiveTransport Aided by Proteins • In facilitated diffusion, transport proteins speed the passive movement of molecules across the plasma membrane • Channel proteins provide corridors that allow a specific molecule or ion to cross the membrane • Channel proteins include – Aquaporins, for facilitated diffusion of water – Ion channels that open or close in response to a stimulus (gated channels) Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 48.
    Fig. 7-15 EXTRACELLULAR FLUID Channel protein (a)A channel protein Solute CYTOPLASM Solute Carrier protein (b) A carrier protein
  • 49.
    • Carrier proteinsundergo a subtle change in shape that translocates the solute-binding site across the membrane Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 50.
    • Some diseasesare caused by malfunctions in specific transport systems, for example the kidney disease cystinuria Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 51.
    Concept 7.4: Activetransport uses energy to move solutes against their gradients • Facilitated diffusion is still passive because the solute moves down its concentration gradient • Some transport proteins, however, can move solutes against their concentration gradients Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 52.
    The Need forEnergy in Active Transport • Active transport moves substances against their concentration gradient • Active transport requires energy, usually in the form of ATP • Active transport is performed by specific proteins embedded in the membranes Animation: Active Transport Animation: Active Transport Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 53.
    • Active transportallows cells to maintain concentration gradients that differ from their surroundings • The sodium-potassium pump is one type of active transport system Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 54.
    Fig. 7-16-1 EXTRACELLULAR FLUID [Na+ ] high [K+ ]low Na+ Na+ Na+ [Na+ ] low [K+ ] high CYTOPLASM Cytoplasmic Na+ binds to the sodium-potassium pump. 1
  • 55.
    Na+ binding stimulates phosphorylation byATP. Fig. 7-16-2 Na+ Na+ Na+ ATP P ADP 2
  • 56.
    Fig. 7-16-3 Phosphorylation causes theprotein to change its shape. Na+ is expelled to the outside. Na+ P Na+ Na+ 3
  • 57.
    Fig. 7-16-4 K+ binds onthe extracellular side and triggers release of the phosphate group. P P K+ K+ 4
  • 58.
    Fig. 7-16-5 Loss ofthe phosphate restores the protein’s original shape. K+ K+ 5
  • 59.
    Fig. 7-16-6 K+ is released,and the cycle repeats. K+ K+ 6
  • 60.
    2 EXTRACELLULAR FLUID [Na+ ] high [K+ ] low [Na+ ]low [K+ ] high Na+ Na+ Na+ Na+ Na+ Na+ CYTOPLASM ATP ADP P Na+ Na+ Na+ P 3 K+ K+ 6 K+ K+ 5 4 K+ K+ P P 1 Fig. 7-16-7
  • 61.
    Fig. 7-17 Passive transport DiffusionFacilitated diffusion Active transport AT P
  • 62.
    How Ion PumpsMaintain Membrane Potential • Membrane potential is the voltage difference across a membrane • Voltage is created by differences in the distribution of positive and negative ions Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 63.
    • Two combinedforces, collectively called the electrochemical gradient, drive the diffusion of ions across a membrane: – A chemical force (the ion’s concentration gradient) – An electrical force (the effect of the membrane potential on the ion’s movement) Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 64.
    • An electrogenicpump is a transport protein that generates voltage across a membrane • The sodium-potassium pump is the major electrogenic pump of animal cells • The main electrogenic pump of plants, fungi, and bacteria is a proton pump Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 65.
  • 66.
    Cotransport: Coupled Transportby a Membrane Protein • Cotransport occurs when active transport of a solute indirectly drives transport of another solute • Plants commonly use the gradient of hydrogen ions generated by proton pumps to drive active transport of nutrients into the cell Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 67.
  • 68.
    Concept 7.5: Bulktransport across the plasma membrane occurs by exocytosis and endocytosis • Small molecules and water enter or leave the cell through the lipid bilayer or by transport proteins • Large molecules, such as polysaccharides and proteins, cross the membrane in bulk via vesicles • Bulk transport requires energy Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 69.
    Exocytosis • In exocytosis,transport vesicles migrate to the membrane, fuse with it, and release their contents • Many secretory cells use exocytosis to export their products Animation: Exocytosis Animation: Exocytosis Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 70.
    Endocytosis • In endocytosis,the cell takes in macromolecules by forming vesicles from the plasma membrane • Endocytosis is a reversal of exocytosis, involving different proteins • There are three types of endocytosis: – Phagocytosis (“cellular eating”) – Pinocytosis (“cellular drinking”) – Receptor-mediated endocytosis Animation: Exocytosis and Endocytosis Introduction Animation: Exocytosis and Endocytosis Introduction Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 71.
    • In phagocytosisa cell engulfs a particle in a vacuole • The vacuole fuses with a lysosome to digest the particle Animation: Phagocytosis Animation: Phagocytosis Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 72.
    Fig. 7-20 PHAGOCYTOSIS EXTRACELLULAR FLUID CYTOPLASM Pseudopodium “Food”or other particle Food vacuole PINOCYTOSIS 1µm Pseudopodium of amoeba Bacterium Food vacuole An amoeba engulfing a bacterium via phagocytosis (TEM) Plasma membrane Vesicle 0.5 µm Pinocytosis vesicles forming (arrows) in a cell lining a small blood vessel (TEM) RECEPTOR-MEDIATED ENDOCYTOSIS Receptor Coat protein Coated vesicle Coated pit Ligand Coat protein Plasma membrane A coated pit and a coated vesicle formed during receptor- mediated endocytosis (TEMs) 0.25 µm
  • 73.
    Fig. 7-20a PHAGOCYTOSIS CYTOPLASM EXTRACELLULAR FLUID Pseudopodium “Food” or otherparticle Food vacuole Food vacuole Bacterium An amoeba engulfing a bacterium via phagocytosis (TEM) Pseudopodium of amoeba 1 µm
  • 74.
    • In pinocytosis,molecules are taken up when extracellular fluid is “gulped” into tiny vesicles Animation: Pinocytosis Animation: Pinocytosis Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 75.
    Fig. 7-20b PINOCYTOSIS Plasma membrane Vesicle 0.5 µm Pinocytosisvesicles forming (arrows) in a cell lining a small blood vessel (TEM)
  • 76.
    • In receptor-mediatedendocytosis, binding of ligands to receptors triggers vesicle formation • A ligand is any molecule that binds specifically to a receptor site of another molecule Animation: Receptor-Mediated Endocytosis Animation: Receptor-Mediated Endocytosis Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 77.
    Fig. 7-20c RECEPTOR-MEDIATED ENDOCYTOSIS Receptor Coatprotein Coated pit Ligand Coat protein Plasma membrane 0.25 µm Coated vesicle A coated pit and a coated vesicle formed during receptor- mediated endocytosis (TEMs)
  • 78.
    Fig. 7-UN1 Passive transport: Facilitateddiffusion Channel protein Carrier protein
  • 79.
  • 80.
    Fig. 7-UN3 Environment: 0.01 Msucrose 0.01 M glucose 0.01 M fructose “Cell” 0.03 M sucrose 0.02 M glucose
  • 81.
  • 82.
    You should nowbe able to: 1. Define the following terms: amphipathic molecules, aquaporins, diffusion 2. Explain how membrane fluidity is influenced by temperature and membrane composition 3. Distinguish between the following pairs or sets of terms: peripheral and integral membrane proteins; channel and carrier proteins; osmosis, facilitated diffusion, and active transport; hypertonic, hypotonic, and isotonic solutions Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
  • 83.
    4. Explain howtransport proteins facilitate diffusion 5. Explain how an electrogenic pump creates voltage across a membrane, and name two electrogenic pumps 6. Explain how large molecules are transported across a cell membrane Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings

Editor's Notes

  • #3 Figure 7.1 How do cell membrane proteins help regulate chemical traffic?
  • #4 For the Cell Biology Video Structure of the Cell Membrane, go to Animation and Video Files.
  • #6 Figure 7.2 Phospholipid bilayer (cross section)
  • #8 Figure 7.3 The fluid mosaic model for membranes
  • #10 Figure 7.4 Freeze-fracture
  • #12 Figure 7.5 The fluidity of membranes
  • #13 Figure 7.5a The fluidity of membranes
  • #14 Figure 7.6 Do membrane proteins move?
  • #16 Figure 7.5b The fluidity of membranes
  • #18 Figure 7.5c The fluidity of membranes
  • #20 Figure 7.7 The detailed structure of an animal cell’s plasma membrane, in a cutaway view
  • #22 Figure 7.8 The structure of a transmembrane protein
  • #24 Figure 7.9 Some functions of membrane proteins
  • #25 Figure 7.9a–c Some functions of membrane proteins
  • #26 Figure 7.9d–f Some functions of membrane proteins
  • #29 Figure 7.10 Synthesis of membrane components and their orientation on the resulting membrane
  • #35 Figure 7.11 The diffusion of solutes across a membrane
  • #36 Figure 7.11a The diffusion of solutes across a membrane
  • #38 Figure 7.11b The diffusion of solutes across a membrane
  • #40 Figure 7.12 Osmosis
  • #42 Figure 7.13 The water balance of living cells
  • #44 Figure 7.14 The contractile vacuole of Paramecium: an evolutionary adaptation for osmoregulation
  • #47 For the Cell Biology Video Water Movement through an Aquaporin, go to Animation and Video Files.
  • #48 Figure 7.15 Two types of transport proteins that carry out facilitated diffusion
  • #53 For the Cell Biology Video Na+/K+ATPase Cycle, go to Animation and Video Files.
  • #54 Figure 7.16, 1 The sodium-potassium pump: a specific case of active transport
  • #55 Figure 7.16, 2 The sodium-potassium pump: a specific case of active transport
  • #56 Figure 7.16, 3 The sodium-potassium pump: a specific case of active transport
  • #57 Figure 7.16, 4 The sodium-potassium pump: a specific case of active transport
  • #58 Figure 7.16, 5 The sodium-potassium pump: a specific case of active transport
  • #59 Figure 7.16, 6 The sodium-potassium pump: a specific case of active transport
  • #60 Figure 7.16, 1–6 The sodium-potassium pump: a specific case of active transport
  • #61 Figure 7.17 Review: passive and active transport
  • #65 Figure 7.18 An electrogenic pump
  • #67 Figure 7.19 Cotransport: active transport driven by a concentration gradient
  • #71 For the Cell Biology Video Phagocytosis in Action, go to Animation and Video Files.
  • #72 Figure 7.20 Endocytosis in animal cells
  • #73 Figure 7.20 Endocytosis in animal cells—phagocytosis
  • #75 Figure 7.20 Endocytosis in animal cells—pinocytosis
  • #77 Figure 7.20 Endocytosis in animal cells—receptor-mediated endocytosis