| Structure of Cell membrane | Lipid Diffusion | Osmosis and Water Potential | Passive Transport (Facilitated Diffusion) | Active Transport | Endocytosis and Exocytosis |
The
Structure of the Cell Membrane
The
cell membrane (or plasma membrane) surrounds all living cells, and is the
cell's most important organelle. It controls how substances can move in and out
of the cell and is responsible for many other properties of the cell as well.
The membranes that surround the nucleus and other organelles are almost
identical to the cell membrane. Membranes are composed of phospholipids,
proteins and carbohydrates arranged in a fluid mosaic structure, as shown
in this diagram.
The phospholipids form a thin, flexible sheet, while the proteins "float" in the phospholipid sheet like icebergs, and the carbohydrates extend out from the proteins.
The phospholipids are arranged in a bilayer, with their polar, hydrophilic phosphate heads facing outwards, and their non-polar, hydrophobic fatty acid tails facing each other in the middle of the bilayer. This hydrophobic layer acts as a barrier to all but the smallest molecules, effectively isolating the two sides of the membrane. Different kinds of membranes can contain phospholipids with different fatty acids, affecting the strength and flexibility of the membrane, and animal cell membranes also contain cholesterol linking the fatty acids together and so stabilising and strengthening the membrane.
The proteins usually span from one side of the phospholipid bilayer to the other (integral proteins), but can also sit on one of the surfaces (peripheral proteins). They can slide around the membrane very quickly and collide with each other, but can never flip from one side to the other. The proteins have hydrophilic amino acids in contact with the water on the outside of membranes, and hydrophobic amino acids in contact with the fatty chains inside the membrane. Proteins comprise about 50% of the mass of membranes, and are responsible for most of the membrane's properties.
Proteins that span the membrane are usually involved in transporting substances across the membrane (more details below).
Proteins on the inside surface of cell membranes are often attached to the cytoskeleton and are involved in maintaining the cell's shape, or in cell motility. They may also be enzymes, catalysing reactions in the cytoplasm.
Proteins on the outside surface of cell membranes can act as receptors by having a specific binding site where hormones or other chemicals can bind. This binding then triggers other events in the cell. They may also be involved in cell signalling and cell recognition, or they may be enzymes, such as maltase in the small intestine (more in digestion).
The carbohydrates are found on the outer surface of all eukaryotic cell membranes, and are attached to the membrane proteins or sometimes to the phospholipids. Proteins with carbohydrates attached are called glycoproteins, while phospholipids with carbohydrates attached are called glycolipids. The carbohydrates are short polysaccharides composed of a variety of different monosaccharides, and form a cell coat or glycocalyx outside the cell membrane. The glycocalyx is involved in protection and cell recognition, and antigens such as the ABO antigens on blood cells are usually cell-surface glycoproteins.
Cell membranes are a barrier to most substances, and this property allows materials to be concentrated inside cells, excluded from cells, or simply separated from the outside environment. This is compartmentalisation is essential for life, as it enables reactions to take place that would otherwise be impossible. Eukaryotic cells can also compartmentalise materials inside organelles. Obviously materials need to be able to enter and leave cells, and there are five main methods by which substances can move across a cell membrane:
Lipid Diffusion
Osmosis
Passive Transport
Active Transport
Vesicles
A
few substances can diffuse directly through the lipid bilayer part of the
membrane. The only substances that can do this are lipid-soluble molecules such
as steroids, or very small molecules, such as H2O, O2 and
CO2. For these molecules the membrane is no barrier at all. Since
lipid diffusion is (obviously) a passive diffusion process, no energy is
involved and substances can only move down their concentration gradient. Lipid
diffusion cannot be controlled by the cell, in the sense of being switched on or
off.
Osmosis is the diffusion of water across a membrane. It is in fact just normal lipid diffusion, but since water is so important and so abundant in cells (its concentration is about 50 M), the diffusion of water has its own name - osmosis. The contents of cells are essentially solutions of numerous different solutes, and the more concentrated the solution, the more solute molecules there are in a given volume, so the fewer water molecules there are. Water molecules can diffuse freely across a membrane, but always down their concentration gradient, so water therefore diffuses from a dilute to a concentrated solution.
Water Potential. Osmosis can be quantified using water potential, so we can calculate which way water will move, and how fast. Water potential (Y, the Greek letter psi, pronounced "sy") is simply the effective concentration of water. It is measured in units of pressure (Pa, or usually kPa), and the rule is that water always "falls" from a high to a low water potential (in other words it's a bit like gravity potential or electrical potential). 100% pure water has Y = 0, which is the highest possible water potential, so all solutions have Y < 0, and you cannot get Y > 0.
Osmotic
Pressure (OP). This is an older term used to describe osmosis. The more
concentrated a solution, the higher the osmotic pressure. It therefore means the
opposite to water potential, and so water move from a low to a high OP. Always
use Y rather than OP.
Cells and Osmosis. The concentration (or OP) of the solution that surrounds a cell will affect the state of the cell, due to osmosis. There are three possible concentrations of solution to consider:
Isotonic solution a solution of equal OP (or concentration) to a cell
Hypertonic solution a solution of higher OP (or concentration) than a cell
Hypotonic solution a solution of lower OP (or concentration) than a cell
The effects of these solutions on cells are shown in this diagram:
These are problems that living cells face all the time. For example:
Simple animal cells (protozoans) in fresh water habitats are surrounded by a hypotonic solution and constantly need to expel water using contractile vacuoles to prevent swelling and lysis.
Cells in marine environments are surrounded by a hypertonic solution, and must actively pump ions into their cells to reduce their water potential and so reduce water loss by osmosis.
Young non-woody plants rely on cell turgor for their support, and without enough water they wilt. Plants take up water through their root hair cells by osmosis, and must actively pump ions into their cells to keep them hypertonic compared to the soil. This is particularly difficult for plants rooted in salt water.
Passive transport is the transport of substances across a membrane by a trans-membrane protein molecule. The transport proteins tend to be specific for one molecule (a bit like enzymes), so substances can only cross a membrane if it contains the appropriate protein. As the name suggests, this is a passive diffusion process, so no energy is involved and substances can only move down their concentration gradient. There are two kinds of transport protein:
Channel Proteins form a water-filled pore or channel in the membrane. This allows charged substances (usually ions) to diffuse across membranes. Most channels can be gated (opened or closed), allowing the cell to control the entry and exit of ions.
Carrier Proteins have a binding site for a specific solute and constantly flip between two states so that the site is alternately open to opposite sides of the membrane. The substance will bind on the side where it at a high concentration and be released where it is at a low concentration.
Active
transport is the pumping of substances across a membrane by a trans-membrane protein
pump molecule. The protein binds a molecule of the substance to be
transported on one side of the membrane, changes shape, and releases it on the
other side. The proteins are highly specific, so there is a different protein
pump for each molecule to be transported. The protein pumps are also ATPase
enzymes, since they catalyse the splitting of ATP g
ADP + phosphate (Pi), and use the energy released to change shape and pump the
molecule. Pumping is therefore an active process, and is the only
transport mechanism that can transport substances up their concentration
gradient.
The Na+K+ Pump. This transport protein is present in the cell membranes of all animal cells and is the most abundant and important of all membrane pumps.
The Na+K+ pump is a complex pump, simultaneously pumping three sodium ions out of the cell and two potassium ions into the cell for each molecule of ATP split. This means that, apart from moving ions around, it also generates a potential difference across the cell membrane. This is called the membrane potential, and all animal cells have it. It varies from 20 to 200 mV, but and is always negative inside the cell. In most cells the Na+K+ pump runs continuously and uses 30% of all the cell's energy (70% in nerve cells).
The
rate of diffusion of a substance across a membrane increases as its
concentration gradient increases, but whereas lipid diffusion shows a linear
relationship, facilitated diffusion has a curved relationship with a maximum
rate. This is due to the rate being limited by the number of transport proteins.
The rate of active transport also increases with concentration gradient, but
most importantly it has a high rate even when there is no concentration
difference across the membrane. Active transport stops if cellular respiration
stops, since there is no energy.
The
processes described so far only apply to small molecules. Large molecules (such
as proteins, polysaccharides and nucleotides) and even whole cells are moved in
and out of cells by using membrane vesicles.
Endocytosis is the transport of materials into a cell. Materials are enclosed by a fold of the cell membrane, which then pinches shut to form a closed vesicle. Strictly speaking the material has not yet crossed the membrane, so it is usually digested and the small product molecules are absorbed by the methods above. When the materials and the vesicles are small (such as a protein molecule) the process is known as pinocytosis (cell drinking), and if the materials are large (such as a white blood cell ingesting a bacterial cell) the process is known as phagocytosis (cell eating).
Exocytosis is the transport of materials out of a cell. It is the exact reverse of endocytosis. Materials to be exported must first be enclosed in a membrane vesicle, usually from the RER and Golgi Body. Hormones and digestive enzymes are secreted by exocytosis from the secretory cells of the intestine and endocrine glands.
Sometimes
materials can pass straight through cells without ever making contact with the
cytoplasm by being taken in by endocytosis at one end of a cell and passing out
by exocytosis at the other end.
Summary of
Membrane Transport
| Method |
Uses
energy |
Uses
proteins |
Specific |
Controllable |
| Lipid Diffusion | N |
N | N | N |
| Osmosis | N |
N |
Y |
N |
| Passive Transport | N |
Y |
Y |
Y |
| Active Transport | Y |
Y |
Y |
Y |
| Vesicles | Y |
N |
Y |
Y |
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Last updated 18/06/2004