Chapter 7-Membrane Structure and Function : Life at The Edge
Chapter 7-Membrane Structure and Function : Life at The Edge
Chapter 7-Membrane Structure and Function : Life at The Edge
HCC-SW/Stafford Campus
Concept 7.1 : Cellular membranes are fluid mosaics of lipids and proteins
The primary components of membranes are lipids and proteins. The most common type of lipid is
phospholipids. A phospholipid is an amphipathic molecule – it has both hydrophilic and hydrophobic regions
(Figure 7.2). Membranes are described using the fluid mosaic model (Figure 7.3). “Mosaic” because of the
various proteins associated with the phospholipids. [See also Inquiry Do membrane proteins move? Figure
7.4.]
The phospholipids of membranes move very easy laterally, and not very easily by flip-flopping. Proteins
associated with the membranes also move through the phospholipids (Figure 7.6). Membranes remain fluid
until a certain temperature at which the phospholipids stop moving. The more phospholipids have
unsaturated fatty acid tails, the more fluid the membrane will remain (Figure 7.5a). In animal cells, the steroid
cholesterol has an effect on the fluidity of the membrane. At body temperature cholesterol makes the
membrane less fluid by restraining phospholipid movement. At lower temperatures cholesterol prevents the
phospholipids from packing close together (Figure 7.5b).
The specific chemical structure of the hydrocarbon tails of phospholipids seems to have evolved such that
different species can exist in different environments. Natural selection has apparently favored organisms
whose mix of membrane lipids ensures an appropriate level of membrane fluidity for their environment.
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BIOL 1406 J.L. Marshall, Ph.D.
HCC-SW/Stafford Campus
The mosaic aspect of membranes comes from the fact that the membrane is a collage of different proteins
clustered in groups, embedded in the fluid matrix of the lipid bilayer. Proteins determine most of the
membrane’s function. There are two main groups of membrane proteins: 1) integral proteins, proteins that
span the width of the phospholipid bilayer. These proteins have a hydrophobic region in area of the fatty acid
tails of phospholipids. The hydrophilic regions of these proteins are exposed on either side of the membrane.
Another term associated with these proteins is transmembrane proteins (Figure 7.6); and 2) peripheral
proteins are not embedded in the lipid bilayer, they are loosely associated to the surface of the membrane.
Figure 7.7 shows the major functions of different membrane proteins. Learning about membrane proteins is
important in the medical field as some microbes use membrane proteins to gain access to entry into the cell,
as seen in HIV (Figure 7.8)
Cell-cell recognition is important for a cell’s ability to recognize different cells. Carbohydrates are important in
this recognition. Glycolipids are carbohydrates that are covalently bonded to lipids. Glycoproteins are
carbohydrates that are covalently bonded to proteins. The glycolipids and glycoproteins are on the external
side of the membrane and allow for distinguishing markers on cells.
Each side of the membrane has a unique composition of lipids and proteins (Figure 7.9).
Certain hydrophobic molecules such as CO2 and O2 can easily cross the cell membrane. Polar molecules do not
pass as easily across the hydrophobic region of the lipid bilayer.
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BIOL 1406 J.L. Marshall, Ph.D.
HCC-SW/Stafford Campus
Transport Proteins
Hydrophilic substances can pass through the lipid bilayer by passing through transport proteins that span the
membrane. Some transport proteins, called channel proteins, have a hydrophilic center that allows charged to
pass across the lipid portion. An example of a channel protein is an aquaporin that allows for the passage of
water across the membrane. Some transport proteins are called carrier proteins that escort their “passengers”
across the membrane. The selective permeability of a membrane depends on both the discriminating barrier
of the lipid bilayer and the specific proteins built into the membrane. There is also direction across the
membrane.
The diffusion of water across a selectively permeable membrane in response to a solute concentration is
called osmosis. Water moves from areas of low solute concentration to areas of higher solute concentration
(Figure 7.11).
Water Balance of Cells Without Walls Tonicity is the ability of a surrounding solution to cause a cell to
gain or lose water. The tonicity of a solution depends on its concentration of solutes that can not cross
the membrane relative to that inside the cell.
An isotonic solution will cause no net movement of water across the plasma membrane. A hypertonic
solution will cause the cell to lose water, and shrivel. A hypotonic solution will cause the cell to swell
because excess water enters the cell (Figure 7.12a). Cells that lack rigid cell walls have other
adaptation to survive called osmoregulation. Paramecium caudatum has a contractile vacuole to expel
excess water (Figure 7.13).
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BIOL 1406 J.L. Marshall, Ph.D.
HCC-SW/Stafford Campus
Water Balance of Cells with Walls Organisms like plants have a cell wall. When excess water enters the
cell, the cell wall opposes further water uptake by a process called turgor pressure. At this point the
cell is turgid. If a plant cell is in an isotonic environment, then it becomes flaccid. If the plant cell is in a
hypertonic solution then it can undergo plasmolysis, which causes plant cell death (Figure 7.12b).
Facilitated diffusion is the transport of molecules across the lipid bilayer by a transport protein that spans the
membrane. Channel proteins allow molecules to easily pass from one side of the membrane to the other
(Figure 7.14a). Channel proteins that transport ions are called ion gated channels that open or close in
response to a stimulus (figure 7.14b). No energy input is required, thus it is passive transport.
Concept 7.4 : Active transport uses energy to move solutes against their gradients
Some transport proteins can move solutes against their concentration gradient across the plasma membrane.
Active transport uses energy to move solutes across the membrane against its concentration gradient. This
type of transport protein is a carrier protein. Active transport enables a cell to maintain internal
concentrations of small solutes that differ from concentrations in its environment. ATP usually supplies the
energy for active transport. The sodium-potassium pump is an example of active transport (Figure 7.15). The
difference between active and passive transport is reviewed in Figure 7.16.
All cells have electrical potential energy across their membrane referred to as voltage. The cytoplasmic side of
the membrane is negatively charged. The voltage across the membrane is called membrane potential. The
membrane potential is like a battery. Due to the charge difference between inside the cell and outside, the
membrane potential favors the passage of cations inside the cell, and anions outside the cell. The
electrochemical gradient describes two forces that that affect ion movement across the membrane: a
chemical force and an electrical force. A transport protein that generates voltage across a membrane is called
an electrogenic pump. The main electrogenic pump of plants is a proton pump (Figure 7.17).
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BIOL 1406 J.L. Marshall, Ph.D.
HCC-SW/Stafford Campus
Cotransport systems couple (pair) the movement of molecules across the membrane in opposite directions.
As one transport protein pumps a molecule out of the cell, its cotransporter pumps a molecule inside the cell.
Energy is used in this process so it is an active transport system (Figure 7.18).
Concept 7.5 : Bulk transport across the plasma membrane occurs by exocytosis and
endocytosis
Large molecules such as proteins can cross the membrane by bulk transport in vesicles. This process requires
energy.
Exocytosis
Exocytosis is the bulk transport process of moving molecules outside the cell. Vesicles bud from the Golgi
apparatus and fuse with the plasma membrane.
Endocytosis
Endocytosis is the bulk transport of molecules moving inside the cell. Types of endocytosis in animal cells are:
1) phagocytosis, 2) pinocytosis, and 3) receptor-mediated endocytosis (Figure 7.19).