Fluid Mosaic Model of Plasma Membrane
Fluid
mosaic model
The currently accepted model for the structure of the plasma membrane,
called the fluid mosaic model, was first
proposed in 1972. This model has evolved over time, but it still provides a
good basic description of the structure and behaviour of membranes in many
cells.
According to the fluid mosaic model, the plasma membrane is a mosaic of
components—primarily, phospholipids, cholesterol, and proteins—that move freely
and fluidly in the plane of the membrane. In other words, a diagram of the
membrane (like the one below) is just a snapshot of a dynamic process in which
phospholipids and proteins are continually sliding past one another.
Interestingly enough, this fluidity means that if you insert a very fine
needle into a cell, the membrane will simply part to flow around the needle;
once the needle is removed, the membrane will flow back together seamlessly.
Image of the plasma membrane, showing
the phospholipid bilayer with peripheral and integral membrane proteins,
glycoproteins (proteins with a carbohydrate attached), glycolipids (lipids with
a carbohydrate attached), and cholesterol molecules.
The principal components of the plasma membrane are lipids
(phospholipids and cholesterol), proteins, and carbohydrate groups that are
attached to some of the lipids and proteins.
- A phospholipid is a lipid made of glycerol, two
fatty acid tails, and a phosphate-linked head group. Biological membranes
usually involve two layers of phospholipids with their tails pointing
inward, an arrangement called a phospholipid bilayer.
- Cholesterol, another lipid composed of
four fused carbon rings, is found alongside phospholipids in the core of
the membrane.
- Membrane proteins may extend
partway into the plasma membrane, cross the membrane entirely, or be
loosely attached to its inside or outside face.
- Carbohydrate groups are
present only on the outer surface of the plasma membrane and are attached
to proteins, forming glycoproteins,
or lipids, forming glycolipids.
The proportions of proteins, lipids, and carbohydrates in the plasma
membrane vary between different types of cells. For a typical human cell,
however, proteins account for about 50 percent of the composition by mass,
lipids (of all types) account for about 40 percent, and the remaining 10
percent comes from carbohydrates.
Phospholipids
Phospholipids, arranged in a bilayer, make up the basic fabric of the
plasma membrane. They are well-suited for this role because they are amphipathic, meaning that they have both hydrophilic
and hydrophobic regions.
Chemical structure of a phospholipid, showing the hydrophilic head and hydrophobic tails.
The hydrophilic, or “water-loving,”
portion of a phospholipid is its head, which contains a negatively charged
phosphate group as well as an additional small group (of varying identity, “R”
in the diagram at left), which may also or be charged or polar. The hydrophilic
heads of phospholipids in a membrane bilayer face outward, contacting the
aqueous (watery) fluid both inside and outside the cell. Since water is a polar
molecule, it readily forms electrostatic (charge-based) interactions with the
phospholipid heads.
The hydrophobic, or “water-fearing,”
part of a phospholipid consists of its long, nonpolar fatty acid tails. The
fatty acid tails can easily interact with other nonpolar molecules, but they
interact poorly with water. Because of this, it’s more energetically favorable for the phospholipids to tuck their fatty acid tails away in the interior of
the membrane, where they are shielded from the surrounding water. The
phospholipid bilayer formed by these interactions makes a good barrier between
the interior and exterior of the cell, because water and other polar or charged
substances cannot easily cross the hydrophobic core of the membrane.
Image of a micelle and a liposome.
Thanks to their amphipathic nature, phospholipids aren’t just
well-suited to form a membrane bilayer. Instead, this is something they’ll do
spontaneously under the right conditions! In water or aqueous solution,
phospholipids tend to arrange themselves with their hydrophobic tails facing
each other and their hydrophilic heads facing out. If the phospholipids have
small tails, they may form a micelle (a
small, single-layered sphere), while if they have bulkier tails, they may form
a liposome (a hollow droplet of bilayer membrane) ^22squared.
Proteins
Proteins are the second major component of plasma membranes. There are
two main categories of membrane proteins: integral and peripheral.
Image of a single-pass transmembrane protein with a single membrane-spanning alpha helix and a three-pass transmembrane protein with three membrane-spanning alpha helices.
Integral membrane proteins are, as their name suggests, integrated into the membrane: they have at least one hydrophobic region that anchors them to the hydrophobic core of the phospholipid bilayer. Some stick only partway into the membrane, while others stretch from one side of the membrane to the other and are exposed on either side^11start superscript, 1, end superscript. Proteins that extend all the way across the membrane are called transmembrane proteins.
The portions of an integral membrane protein found inside the membrane
are hydrophobic, while those that are exposed to the cytoplasm or extracellular
fluid tend to be hydrophilic. Transmembrane proteins may cross the membrane
just once, or may have as many as twelve different membrane-spanning sections.
A typical membrane-spanning segment consists of 20-25 hydrophobic amino acids
arranged in an alpha helix, although not all transmembrane proteins fit this model. Some
integral membrane
proteins form a channel that allows ions or other small molecules to pass, as
shown below.
Peripheral membrane proteins are found on the outside and inside surfaces of membranes, attached either to integral proteins or to phospholipids. Unlike integral membrane proteins, peripheral membrane proteins do not stick into the hydrophobic core of the membrane, and they tend to be more loosely attached.
Carbohydrates
Carbohydrates are the third major component of plasma membranes. In
general, they are found on the outside surface of cells and are bound either to
proteins (forming glycoproteins) or to lipids
(forming glycolipids). These carbohydrate chains may consist of
2-60 monosaccharide units and can be either straight or branched.
Along with membrane proteins, these carbohydrates form distinctive
cellular markers, sort of like molecular ID badges, that allow cells to
recognize each other. These markers are very important in the immune system,
allowing immune cells to differentiate between body cells, which they shouldn’t
attack, and foreign cells or tissues, which they should.
Membrane fluidity
The structure of the fatty acid tails of the phospholipids is important
in determining the properties of the membrane, and in particular, how fluid it
is.
Saturated fatty acids
have no double bonds (are saturated with hydrogens), so they are relatively
straight. Unsaturated fatty acids, on
the other hand, contain one or more double bonds, often resulting in a bend or
kink. (You can see an example of a bent, unsaturated tail in the diagram of
phospholipid structure that appears earlier in this article.) The saturated and
unsaturated fatty acid tails of phospholipids behave differently as temperature
drops:
- At cooler temperatures, the
straight tails of saturated fatty acids can pack tightly together, making
a dense and fairly rigid membrane.
- Phospholipids with
unsaturated fatty acid tails cannot pack together as tightly because of
the bent structure of the tails. Because of this, a membrane containing
unsaturated phospholipids will stay fluid at lower temperatures than a
membrane made of saturated ones.
Most cell membranes contain a mixture of phospholipids, some with two saturated (straight) tails and others with one saturated and one unsaturated (bent) tail. Many organisms—fish are one example—can adjust physiologically to cold environments by changing the proportion of unsaturated fatty acids in their membranes. For more information about saturated and unsaturated fatty acids, see the article on lipids.
In addition to phospholipids, animals have an additional membrane
component that helps to maintain fluidity. Cholesterol, another
type of lipid that is embedded among the phospholipids of the membrane, helps
to minimize the effects of temperature on fluidity.
At low temperatures, cholesterol increases fluidity by keeping
phospholipids from packing tightly together, while at high temperatures, it
actually reduces fluidity^{3,4}3,4start superscript, 3, comma, 4, end
superscript. In this way, cholesterol expands the range of temperatures
at which a membrane maintains a functional, healthy fluidity.
The components of the plasma membrane
|
Component |
Location |
|
Phospholipids |
Main fabric of
the membrane |
|
Cholesterol |
Tucked between
the hydrophobic tails of the membrane phospholipids |
|
Integral proteins |
Embedded in the
phospholipid bilayer; may or may not extend through both layers |
|
Peripheral
proteins |
On the inner or
outer surface of the phospholipid bilayer, but not embedded in its
hydrophobic core |
|
Carbohydrates |
Attached to
proteins or lipids on the extracellular side of the membrane (forming
glycoproteins and glycolipids) |
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