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I.B.
Biology – Unit 1, Cells
The Cell theory:
1. The cell is the basic unit of life
2. All living things are composed of cells
3. Cells can only come from other (pre-existing) cells
Contributors to cell theory
Time
Contribution
Jansen
Aprox. 1590
Developed 1st compound
microscope
Hooke
1663
Named the cell
Examined Cork cells
under microscopes
Van Leeuwenhoek
1675
Ground lenses to make
powerful microscopes
(aprox. 200X)
Observed blood cells,
and bacteria, and
protozoa.
Oken
1805
“All living things
originate from and are
made of cells”
Brown
1833
Discovered and named
the nucleus
Schleiden
1838
Studied plant cells
All plant cells had a
nucleus
Schwann
1839
Studied animal cells
All animal cells had a
nucleus
Virchow
1855
“All cells come from pre-
existing cells”
Pasteur
1860
Did experiments to
disprove spontaneous
generation
Differences
between
plant cells
and
animal
cells:
Plant Cells
Animal Cells
Have a cell wall
Have chloroplasts
Have no flagellum
Have a larger central vacuole
Have no centrioles
Have no cell walls
Have no chloroplasts
Can have a flagellum
Smaller vacuole, if present
Have centrioles
Differences between prokaryotic and
eukaryotic cells:
Prokaryotic
Eukaryotic
Have pili
No nucleus
DNA is in cytoplasm and it is “naked”
Reproduce using binary fission (Pg. 215
figure 12.10)
No formal organelles (e.g. mitochondria,
E.R., etc…)
Have 70S ribosomes
Have no pili
Have a nucleus
DNA is in nucleus and associated with
proteins
Divide using mitosis/meiosis
Have membrane bound organelles
Have 80S ribosomes
Phospholipids:
A phospholipid is an amphipatic molecule, meaning that is
has both a hydrophilic region (dissolves in
water) and a hydrophobic region (does not dissolve in
water). At the surface of a cell, phospholipids are
arranged in a bilayer, or double layer. The hydrophilic heads
of the molecules are on the outside of the
bilayer, in contact with the aqueous solutions inside and
outside of the cell. The hydrophobic tails point
toward the interior of the membrane, away from the water.
The phospholipid bilayer forms a boundary
between the cell and its external environment.
Cell Membrane: The fluid mosaic model
How do proteins fit into the cell membrane?
Unlike
proteins
dissolved
in the
cytosol,
membrane
proteins
are
n
ot very
soluble in water . Membrane proteins have hydrophilic and
hydrophobic regions ; they are amphipathic, as
are their phospholipid partners in membranes. If proteins
were layered on the surface of the membrane,
their hydrophobic parts would be in an aqueous
environment. Proteins are placed in a location compatible
with their amphipathic character. Membrane proteins are
dispersed and individually inserted into the
phospholipid bilayer, with only their hydrophilic regions
protruding far enough from the bilayer to be
exposed to water. This molecular arrangement would
maximize contact of hydrophilic regions of proteins
and phospholipids with water while providing their
hydrophobic parts with a non aqueous environment.
According to this model, the membrane is a mosaic of
protein molecules bobbing in a fluid bilayer of
phospholipids ; hence the term fluid mosaic model.
What is meant by selectively permeable?
Selectively permeable means that the cell membrane can
select what goes in and out, such as water or
ions. For example the hydrophobic core of the membrane
impedes the transport of ions and polar
molecules, which are hydrophilic. Cell membranes also use
transport proteins to allow certain molecules to
pass through it. Each transport protein is specific for the
substances it translocates (moves), allowing only
a certain substance of closely related substances to cross
the membrane. For example, glucose carried in
blood to the human liver enters liver cells rapidly through
specific transport proteins in the plasma
membrane.
How is the Membrane a fluid mosaic model?
Fluid = can flow/has movement
Mosaic = Made of different components
The cell membrane has a hydrophobic as well as a
hydrophilic region because it’s a phospholipid bilayer
(made up of phospholipids).
The cell membrane contains proteins
Transmembrane proteins (span the bilayer)
Integral proteins –only inside the membrane
Peripheral proteins
Glyco proteins (act as a receptor/landing sites
Cholesterol inside the bilayer (cholesterols makes the bilayer
fluid)
How things go in and out of the cell
1)Passive transport
movement of moleculeswithout spending energy
movement DOWN concentration gradient
a) Simple Diffusion
movement of molecules down concentration gradient
through cell membrane
ex: 02 and other small molecules
b) Osmosis
diffusion of water through a membrane. Water moves from
where there is more (dilute solution) to
where there is less water (high concentration)
Osmotic Conditions:
•
Isotonic solution: same concentration
•
Hypertonic solution: solution is more concentrated
•
Hypotonic solution : solution that is less concentrated
c) Facilitated diffusion:
Specialized transport proteins allow particles to diffuse
Proteins are highly selective, based on size, shape, and
charge.
Carrier proteins (ferry) :
Protein that “carries” substances across
Channel proteins (tunnel):
Tunnel for particles
Usually charged particles
2)Active transport:
Active transport is when transport proteins can move solutes
against their concentration gradients, across the plasma
membrane from the side where they are less concentrated to
the side where they are more concentrated. This transport is
“uphill” and therefore requires work. To pump a molecule
across a membrane against its gradient, the cell must
expand its own metabolic energy ; therefore, this type of
membrane traffic is called active transport. Active transport
is a major factor in the ability of a cell to maintain internal
concentration of small molecules that differ from
concentrations in its environment. For example, compared to
its surroundings, an animal cell has a much higher
concentration of potassium ions and a much lower
concentration of sodium ions. The plasma membrane helps
maintain these steep gradients by pumping sodium out of
the cell, and potassium into the cell. One example of this
happening is the sodium-potassium pump, which exchanges
sodium for potassium across the plasma membrane of
animal cells. The membrane potential, the voltage across a
membrane, acts like a battery, an energy source that affects
the traffic of all charged substances across the membrane.
Because the inside of the cell is negative compared to the
outside, the membrane potential favours the passive
transport of cations into the cell, and anions out of the cell,.
Thus, not one (as in simple diffusion) but two forces drive the
diffusion of ions across the membrane: a chemical force (the
ion’s concentration gradient) and an electrical force (the
effect of the membrane potential on the membrane potential
on the ion’s movement). This combination of forces acting on
an ion is called the electrochemical gradient. An ion does not
simply diffuse down its concentration gradient, but diffuses
down its electrochemical gradient. For example, the
concentration of sodium ions (Na+) inside a resting nerve
cell is much lower than outside it. When the cell is
stimulated, gated channels that facilitate Na+ diffusion will
open. Sodium ions then “fall” down their electrochemical
gradient, driven by the concentration gradient of Na+ and by
the attraction of cations to the negative side of the
membrane, resulting in concentration of Na+ building up on
one side of the membrane. Some membrane proteins that
actively transport ions contribute to the membrane potential.
For example, the aforementioned sodium-potassium pump.
The pump does not actually translocate Na and K one for
one, but actually pumps three sodium ions for every two
potassium ions it pumps into the cell. With each crank of the
pump, there is a net transfer of one positive charge from the
cytoplasm to the extracellular fluid, a process that stores
energy in the form of voltage. Large molecules, such as
proteins, generally cross the membrane by a different
process than their smaller compatriots. They become
transported by either exocytosis or endocytosis. (For the
purpose of this question, we will not explore exocytosis). In
endocytotsis, the cell takes in macromolecules and
particulate matter by forming new vesicles from the plasma
membrane. A small area of the plasma membrane sinks
inward to form a pocket. As the pocket deepens, it pinches
in, forming a vesicle containing material that had been
outside the cell. Phagocytosis, and pinocytosis are both
types of endocytosis. In phagocytosis, a cell engulfs a
particle by wrapping pseudopodia (a cellular extension of
amoeboid cells used in moving and feeding.) around it and
packaging it within a membrane-enclosed sac large enough
to be classified as a vacuole. The particle is digested after
the vacuole fuses with a lyosome containing hydrolytic
enzymes. In pinocytosis, the cells “gulps” droplets of
extracellular fluid in tiny vesicles. Because any and all
solutes dissolved in the droplet are taken into the cell,
pinocytosis is unspecific in the substances it transports. As
can be seen, active transport is very important towards cell
function.
Exocytosis: See figure 8.7 on page 135
Exocytosis is when the cell secretes macromolecules by the
fusion of vesicles with the plasma membrane (exportation).
A transport vesicle budded from the golgi apparatus is
moved by the cytoskeleton to the plasme membrane. When
the vesicle membrane and the plama membrane come into
contact, the lipid molecules of the two bilayers rearrange
themselves so that the two membranes fuse.
BioFactsheet
The Cell Surface Membrane
September 1997
Number 8
1
The cell surface membrane (formerly called the plasma membrane) surrounds the cytoplasm of eukaryotic cells. The
membrane forms a selectively permeable barrier, controlling the substances that enter and leave the cell and therefore
enables the cell to regulate its internal environment.
2. Glycolipids - which make up 5% of membrane lipids. Glycolipids occur on the external surface of the cell surface membrane and the
carbohydrate portion of the glycolipid extends into the intercellular space and is called aglycocalyx. These are important in cell-to-
cell recognition.
3. Cholesterol - a steroid which makes up 20% of lipids in animal
membranes but is rarely found in plant cell membranes.
All lipids can move sideways (laterally) within the membrane and exchange position with each other. This gives the membranefluidity
which is essential in processes such as phagocytosis. The degree of fluidity of cell surface membranes is determined by:
1. The length of the fatty acid side chains (the longer the chains, the
lower the fluidity).
2. The proportion of the fatty acids which are saturated (the higher the
percentage of saturated fats, the lower the fluidity).
3. The steroid content (the higher the steroid content, the lower the
fluidity).
Structure
The cell surface membrane is approximately 7.5nm thick and consists of a bilayer of lipids along with a highly variable component
of protein. Some of these proteins are embedded in the surface of the membrane whilst others (intrinsic proteins) span the entire
width of the membrane. This is known as the fluid mosaic model (Fig 1).
Lipids
There are three types of lipid in the cell surface membrane.
1. Phospholipids - which make up 75% of the lipid. Phospholipids are amphipathic molecules - this means that they have a dual nature in that
one end of the phospholipids (the phosphate group) is hydrophilic (water-loving and polar) whilst the other end of the phospholipid (the
fatty acid chains) is hydrophobic and non-polar. The phospholipid bilayer forms spontaneously with the non-polar fatty acid chains
facing inwards towards each other and the polar phosphate groups facing outwards into the extra-cellular fluid and the inside of the
The interaction between the hydrophobic and hydrophilic ends helps give the membrane stability and it is also these lipids which
give the membrane selective permeability. Lipid soluble (hydrophobic) molecules easily pass through the membrane by diffusion
whilst hydrophilic substances cannot diffuse through; instead they cross the membrane via water-filled pores or channels in
intrinsic proteins.
Fig 1. The fluid mosaic model of the cell surface membrane
Key
A: phospholipid bilayer≈
7.5nm thick
model (fluid mosaic) a surprising number of candidates are unable to sketch the arrangement of phospholipids in the model.
Similarly many candidates appear confused about which part of the phospholipid molecule is polar.
The phospholipid bilayer
1. To act as channels. By maintaining very different concentrations of ions on either side of the membrane, the cell surface membrane maintains an
electrochemical gradient between the inside and outside of the cell which is essential for the efficient functioning of, for example, the
sodium/potassium pump.
2. Transporters. For example, some proteins are able to identify and attach to specific substances such as nutrients, neurotransmitters or
hormones.
3. Receptors. Some proteins recognise and bind to target molecules such as hormones. For example, the surface membrane of cells in the
As in lipids, intrinsic proteins have a hydrophobic and hydrophilic region and the interaction between these regions confers stability on
the membrane. Extrinsic proteins are embedded in, but do not span, the membrane and many have a carbohydrate portion
The rate of diffusion is proportional to the concentration gradient but is also influenced by the size of the ions and the distance over which the
diffusion must occur. Substances which can diffuse across the cell surface membrane include oxygen, carbon dioxide, steroids, the fat-
as the diffusion of water molecules from a region where they are at a high concentration to a region where they are at a low
concentration through a partially permeable membrane. The cell effectively controls the amount of water which enters across the
plasma membrane by regulating the concentration of ions in the cytoplasm via the sodium/potassium pump.
3. Facilitated diffusion. This is considerably faster than normal
diffusion and is used to transport molecules such as glucose, fructose, non
fat-soluble vitamins, urea and many ions across the membrane.
Using the transport of glucose as an example, there are four key steps in
facilitated diffusion:
(i) The outside of the cell surface membrane contains transport protein molecules which bind with glucose. Different cells have different
(iii) The glucose is transported through the membrane to the other side.
(iv) The glucose detaches from the transporter protein and the protein
reverts to its original shape. The glucose is then immediately
phosphorylated. This keeps the concentration of free glucose inside
the cell very low, so maintaining the diffusion gradient.
The rate of facilitated diffusion is proportional to the concentration gradient and to the number of channels or transporter proteins that
are available. The key point to remember is that facilitated diffusion occurs along and not against the normal diffusion gradient.
4. Active Transport.Ions such as sodium (Na+), potassium (K+),
chloride (Cl-), hydrogen (H+) and molecules such as amino acids and glucose may be transported across the cell surface membrane actively
- i.e. ATP is required and the movement is against the concentration gradient. Note that all of these substances can cross the membrane by
facilitated diffusion if the concentration gradient is the right way round and if transporter channels are available.
Active transport commonly involves a protein which acts as a Na+/K+
pump. Most cells have hundreds of these pumps per square micron.
The Na+/K+ pump
(i) On the inside of the cell sodium ions bind to the membrane
(ii) This triggers the breakdown of ATP into ADP and the energy which is
released is used to phosphorylate the protein which forms the pump.
(iii) The protein changes shape and sodium is transported to the outside of
the cell.
(iv) The changed shape of the cell now allows potassium ions on the outside
of the cell to bind to the protein.
(v) This triggers dephosphorylation of the protein - that is, the phosphate
group is removed.
(vi) This changes the shape of the protein and potassium is transported to
the inside of the cell.
(vii)There is a tendency for sodium ions to diffuse back into the cell and
potassium ions back out of the cell. Since the membrane is more
permeable to potassium that sodium, more ions leave the cell than
enter. This reduces the tendency of water to enter the cell by osmosis
Occasionally, application questions are set which test, for example, a candidate’s ability to infer that the mechanism by which
insulin homeostatically regulates blood concentration of glucose is by altering the rate of facilitated diffusion into cells.
Exam Hint - Most candidates are able to differentiate between simple
diffusion and active transport but very few seem able to relate the properties of substances to the mechanism by which they are
able to cross the cell surface membrane and enter cells. Also, candidates show great confusion between facilitated diffusion and
active transport.
It is transport proteins of this kind which are used to actively transport substances such as glucose against their concentration
gradient in the epithelial cells of the ileum and the proximal convoluted tubule cells of the nephron.
Active transport of glucose:
(i) Sodium ions are pumped out of the cell against the electrochemical
gradient.
(ii) Glucose molecules and sodium ions bind to transport proteins which
span the membrane.
(iii) Sodium ions then diffuse back across the membrane i.e. into the cell
carrying glucose with them.
(iv) Glucose and sodium ions move apart once they are in the cell. Through
this mechanism, glucose can be concentrated in particular cells,
sometimes against huge concentration gradients.
Practice Questions
1. The diagram shows part of the cell surface membrane
(a) Identify structure:
(i)
X
(1 mark)
(ii)
Y
(1 mark)
(iii) Z
(1 mark)
(b) State one function of structure X.
(1 mark)
(c)
(i) Explain why the cell surface membrane can be said to be fluid.
(1 mark)
(ii) Outline one way in which membrane fluidity is essential to
cell function.
(2 marks)
2. Complete the table below which compares the processes of
diffusion, facilitated diffusion and active transport.
(4 marks)
Answers
Semicolons indicate marking points.
1. (a) (i)
Glycocalyx;
(ii)
Phospholipid bilayer;
(iii) Intrinsic protein;
(b) Cell recognition/receptor;
(c) (i) Lipids/proteins can move laterally/change places;
(ii)Allows endo/exocytosis;
eg. phagocytes attacking pathogens;
eg. pinocytosis;
(any two)
2.
Endocytosis
Phagocytosis and pinocytosis are different forms of endocytosis - when substances are taken into the cell across the plasma
membrane through the formation of vesicles. In phagocytosis, solid particles or substances which are too large to cross the
membrane are taken into the cell, whereas in pinocytosis, minute droplets of extra-cellular fluid are taken into the cell. In
phagocytosis, the cell surface membrane produces two extensions called pseudopodia which surround the solid particle which is
to be taken into the cell. The pseudopodia fuse and create a vacuole around the particle. In pinocytosis, the cell surface
membrane invaginates, which allows the fluid to flow inwards. The liquid is then enclosed within a vesicle. Both phagocytosis and
pinocytosis are only possible as a result of thef l u i d i t y of the membrane which is itself determined by the lipids of the
membrane.