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 Cell membrane & Transport
© 2009 Ebneshahidi
 Cell membrane & Transport
Dr. Ali Ebneshahidi
Cell Membrane
 To enclose organelles and other contents in cytoplasm.
 To protect the cell.
 To allow substances into and out of the cell.
 To have metabolic reactions on its surface.
© 2009 Ebneshahidi
 "Fluid mosaic model suggests" that the phospholipids form a
bilayer framework, with their hydrophilic (polar) heads on the
surface and their hydrophobic (nonpolar) tails on the inside.
Proteins are embedded in the phospholipids bilayers.
Experimental data have indicated that the proteins the in this
model are securely held to the phospholipids, making the
structure very stable.
Fluid Mosaic Model
© 2009 Ebneshahidi
Functions of Membrane Proteins
 Transport
 Enzymatic activity
© 2009 Ebneshahidi
 Enzymatic activity
 Receptors for signal
transduction
Membrane permeability
 small, hydrophobic or fat-soluble molecules, such as oxygen,
cross the cell membrane quite readily because of "fat
dissolving fat" interaction.
 small, uncharged, hydrophilic or water-soluble molecules,
such as water and carbon dioxide, would also be able to cross
the cell membrane although there is no "fat dissolving fat"
© 2009 Ebneshahidi
the cell membrane although there is no "fat dissolving fat"
interaction.
 large, hydrophilic molecules are usually impermeable to cell
membrane.
 Any molecules carrying strong electrical charges (i.e. ions) are
always impermeable to cell membrane, unless transported by
special mechanisms.
Movements across the cell membrane
Simple diffusion
 Spontaneous phenomenon where small, hydrophobic molecules move
from a higher concentrated area to lower concentrated area.
 All molecules have motion called Brownian Movement, and a
concentration gradient (the difference in two concentrated areas)
© 2009 Ebneshahidi
will always move molecules to the less concentrated area.
 No external energy is required.
 Diffusion stops when equilibrium is achieved (no concentration
gradient).
 Factors that affect diffusion rate includes temperature, concentration,
molecular size, and diffusion distance.
DIFFUSION
© 2009 Ebneshahidi
Facilitated diffusion
• allow large, hydrophilic molecules to cross the cell membrane.
• molecules bind with a specific protein carrier at the cell membrane.
The combined molecule is now fat soluble and can diffuse to the other
side.
• Movement is from a higher concentrated area to a lower concentrated
© 2009 Ebneshahidi
• Movement is from a higher concentrated area to a lower concentrated
area.
• No external energy is required.
Diffusion rate depends largely on the number of protein carriers
available; when all proteins carriers are bound "saturation" occurs and
the diffusion rate stabilizes.
Diffusion Through the Plasma Membrane
© 2009 Ebneshahidi
Osmosis
 movement of water molecules from a higher concentrated area to
a lower concentrated area.
 usually goes to the opposite direction of solute movement.
 water always diffuses to an area with a higher osmotic pressure
© 2009 Ebneshahidi
 water always diffuses to an area with a higher osmotic pressure
(where there is more solutes and less water).
 Because of osmosis, cells respond differently when they are
placed in different osmotic pressure settings.
Filtration
 passage of substances through a membrane (e.g. capillary
wall) by diffusion or osmosis, aided by hydrostatic pressure.
 usually referred to as the separation of solute from solvent in a
solution .
© 2009 Ebneshahidi
 hydrostatic pressure forces water to the other side of the
membrane.
 Important in absorption and excretion processes.
 Molecules move across
the cell membrane from
a lower concentrated
area to a higher
concentrated area.
 Requires external
energy and a protein
carrier.
Active transport
© 2009 Ebneshahidi
carrier.
 Critical in maintaining
homeostasis by
allowing important
substances (e.g.
nutrient molecules) to
move against their
concentration gradients.
Binding of cytoplasmic Na+ to
the pump protein stimulates
phosphorylation by ATP.
1
2 Phosphorylation causes the
protein to change its shape.
6 K+ is released and Na+ sites
are ready to bind Na+
again; the cycle repeats.
Extracellular
fluid
Cytoplasm
Sodium-Potassium Pump
© 2009 Ebneshahidi
3
4
protein to change its shape.
The shape change expels
Na+ to the outside, and
extracellular K+ binds.
5 Loss of phosphate
restores the original
conformation of the
pump protein. K+ binding triggers
release of the
phosphate group.
Concentration gradients
of K+ and Na+
Functions of Membrane Proteins
 Intercellular adhesion
 Cell-cell recognition
© 2009 Ebneshahidi
 Attachment to
cytoskeleton and
extracellular matrix
• Endocytosis: allows large molecule that cannot be transported by other
methods to enter the cell by membrane vesicles.
• Pinocytosis: transports liquid substances, while "phagocytosis"
transports solid substances.
•Divided into 3 main phases – adhesion, ingestion, and digestion.
© 2009 Ebneshahidi

• Exocytosis Allows large molecule that cannot be transported by other
methods to exit the cell membrane.
© 2009 Ebneshahidi

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Chap 3 Cell Membrane.pdf

  • 1.  Cell membrane & Transport © 2009 Ebneshahidi  Cell membrane & Transport Dr. Ali Ebneshahidi
  • 2. Cell Membrane  To enclose organelles and other contents in cytoplasm.  To protect the cell.  To allow substances into and out of the cell.  To have metabolic reactions on its surface. © 2009 Ebneshahidi  "Fluid mosaic model suggests" that the phospholipids form a bilayer framework, with their hydrophilic (polar) heads on the surface and their hydrophobic (nonpolar) tails on the inside. Proteins are embedded in the phospholipids bilayers. Experimental data have indicated that the proteins the in this model are securely held to the phospholipids, making the structure very stable.
  • 3. Fluid Mosaic Model © 2009 Ebneshahidi
  • 4. Functions of Membrane Proteins  Transport  Enzymatic activity © 2009 Ebneshahidi  Enzymatic activity  Receptors for signal transduction
  • 5. Membrane permeability  small, hydrophobic or fat-soluble molecules, such as oxygen, cross the cell membrane quite readily because of "fat dissolving fat" interaction.  small, uncharged, hydrophilic or water-soluble molecules, such as water and carbon dioxide, would also be able to cross the cell membrane although there is no "fat dissolving fat" © 2009 Ebneshahidi the cell membrane although there is no "fat dissolving fat" interaction.  large, hydrophilic molecules are usually impermeable to cell membrane.  Any molecules carrying strong electrical charges (i.e. ions) are always impermeable to cell membrane, unless transported by special mechanisms.
  • 6. Movements across the cell membrane Simple diffusion  Spontaneous phenomenon where small, hydrophobic molecules move from a higher concentrated area to lower concentrated area.  All molecules have motion called Brownian Movement, and a concentration gradient (the difference in two concentrated areas) © 2009 Ebneshahidi will always move molecules to the less concentrated area.  No external energy is required.  Diffusion stops when equilibrium is achieved (no concentration gradient).  Factors that affect diffusion rate includes temperature, concentration, molecular size, and diffusion distance.
  • 8. Facilitated diffusion • allow large, hydrophilic molecules to cross the cell membrane. • molecules bind with a specific protein carrier at the cell membrane. The combined molecule is now fat soluble and can diffuse to the other side. • Movement is from a higher concentrated area to a lower concentrated © 2009 Ebneshahidi • Movement is from a higher concentrated area to a lower concentrated area. • No external energy is required. Diffusion rate depends largely on the number of protein carriers available; when all proteins carriers are bound "saturation" occurs and the diffusion rate stabilizes.
  • 9. Diffusion Through the Plasma Membrane © 2009 Ebneshahidi
  • 10. Osmosis  movement of water molecules from a higher concentrated area to a lower concentrated area.  usually goes to the opposite direction of solute movement.  water always diffuses to an area with a higher osmotic pressure © 2009 Ebneshahidi  water always diffuses to an area with a higher osmotic pressure (where there is more solutes and less water).  Because of osmosis, cells respond differently when they are placed in different osmotic pressure settings.
  • 11. Filtration  passage of substances through a membrane (e.g. capillary wall) by diffusion or osmosis, aided by hydrostatic pressure.  usually referred to as the separation of solute from solvent in a solution . © 2009 Ebneshahidi  hydrostatic pressure forces water to the other side of the membrane.  Important in absorption and excretion processes.
  • 12.  Molecules move across the cell membrane from a lower concentrated area to a higher concentrated area.  Requires external energy and a protein carrier. Active transport © 2009 Ebneshahidi carrier.  Critical in maintaining homeostasis by allowing important substances (e.g. nutrient molecules) to move against their concentration gradients.
  • 13. Binding of cytoplasmic Na+ to the pump protein stimulates phosphorylation by ATP. 1 2 Phosphorylation causes the protein to change its shape. 6 K+ is released and Na+ sites are ready to bind Na+ again; the cycle repeats. Extracellular fluid Cytoplasm Sodium-Potassium Pump © 2009 Ebneshahidi 3 4 protein to change its shape. The shape change expels Na+ to the outside, and extracellular K+ binds. 5 Loss of phosphate restores the original conformation of the pump protein. K+ binding triggers release of the phosphate group. Concentration gradients of K+ and Na+
  • 14. Functions of Membrane Proteins  Intercellular adhesion  Cell-cell recognition © 2009 Ebneshahidi  Attachment to cytoskeleton and extracellular matrix
  • 15. • Endocytosis: allows large molecule that cannot be transported by other methods to enter the cell by membrane vesicles. • Pinocytosis: transports liquid substances, while "phagocytosis" transports solid substances. •Divided into 3 main phases – adhesion, ingestion, and digestion. © 2009 Ebneshahidi 
  • 16. • Exocytosis Allows large molecule that cannot be transported by other methods to exit the cell membrane. © 2009 Ebneshahidi