Facilitated diffusion: Difference between revisions

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=== Basic Features<br> ===
=== Basic Features<br> ===


The bilayer consists of lipids therefore only lipid-soluble molecules can pass through. This is mainly small polar uncharged molecules and small hydrophobic molecules. Facilitated diffusion is a passive process that requires no use of external energy<ref name="null">Dee Unglaub Silverthorn (2010). Human Physiology. 5th Edition. Pearson Internation Edition. Page 145-146.</ref>. The molecules move across the membrane from an area of high concentration to an area of low concentration. If the solute carries a net charge for example, molecules will move down its electrochemical gradient<ref name="null">Alberts et al (2002). Molecular Biology of the Cell. 4th Edition. US Garland Science. Page 618.</ref>.<br>Sugars and amino acids are examples of molecules that move across the plasma membrane using facilitated diffusion. Also, GLUT transporters are a group of carrier proteins that move glucose sugars and associated hexose sugars across the plasma membrane<ref name="null">Dee Unglaub Silverthorn (2010). Human Physiology. 5th Edition. Pearson Internation Edition. Page 145-146.</ref>.  
The bilayer consists of lipids therefore only lipid-soluble molecules can pass through. This is mainly small polar uncharged molecules and small hydrophobic molecules. Facilitated diffusion is a passive process that requires no use of external energy<ref name="null">Dee Unglaub Silverthorn (2010). Human Physiology. 5th Edition. Pearson Internation Edition. Page 145-146.</ref>. The molecules move across the membrane from an area of high concentration to an area of low concentration. If the solute carries a net charge for example, molecules will move down its electrochemical gradient<ref name="second">Alberts et al (2002). Molecular Biology of the Cell. 4th Edition. US Garland Science. Page 618.</ref>.<br>Sugars and amino acids are examples of molecules that move across the plasma membrane using facilitated diffusion. Also, GLUT transporters are a group of carrier proteins that move glucose sugars and associated hexose sugars across the plasma membrane<ref name="null">Dee Unglaub Silverthorn (2010). Human Physiology. 5th Edition. Pearson Internation Edition. Page 145-146.</ref>.  


=== Carrier proteins<br> ===
=== Carrier proteins<br> ===


These are proteins that span the plasma membrane. Each protein carrier is specific to bind to a complementary molecule. On one side of the membrane (higher concentration of molecules), the molecules bind to the carrier protein. The carrier then changes conformational shape to release the molecules on the other side of the membrane (where there is a lower concentration of the molecules)<ref>Barry G. Hinwood (1992). A Textbook of Science for the Health Professions. Nelson Thornes. Page 255-256.</ref>.  
These are proteins that span the plasma membrane. Each protein carrier is specific to bind to a complementary molecule. On one side of the membrane (higher concentration of molecules), the molecules bind to the carrier protein. The carrier then changes conformational shape to release the molecules on the other side of the membrane (where there is a lower concentration of the molecules)<ref name="third">Barry G. Hinwood (1992). A Textbook of Science for the Health Professions. Nelson Thornes. Page 255-256.</ref>.  


=== Factors affecting rate of facilitated diffusion  ===
=== Factors affecting rate of facilitated diffusion  ===
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1. Difference in concentration between the two sides of the membrane.<br>2. The frequency of carrier proteins available on the plasma membrane.<br>3. The time taken for the molecule to bind with the carrier protein.<br>4. Type of carrier protein utilized as some carriers are also specific to similar shaped molecules.<br>
1. Difference in concentration between the two sides of the membrane.<br>2. The frequency of carrier proteins available on the plasma membrane.<br>3. The time taken for the molecule to bind with the carrier protein.<br>4. Type of carrier protein utilized as some carriers are also specific to similar shaped molecules.<br>


<ref>Barry G. Hinwood (1992). A Textbook of Science for the Health Professions. Nelson Thornes. Page 255-256.</ref>
<ref name="third">Barry G. Hinwood (1992). A Textbook of Science for the Health Professions. Nelson Thornes. Page 255-256.</ref>  


=== References  ===
=== References  ===


<references />
<references />

Revision as of 19:47, 27 November 2011

Facilitated diffusion

Facilitated diffusion is the movement of lipid insoluble molecules across the phospholipid bilayer by the use of carrier proteins[1].

Basic Features

The bilayer consists of lipids therefore only lipid-soluble molecules can pass through. This is mainly small polar uncharged molecules and small hydrophobic molecules. Facilitated diffusion is a passive process that requires no use of external energy[1]. The molecules move across the membrane from an area of high concentration to an area of low concentration. If the solute carries a net charge for example, molecules will move down its electrochemical gradient[2].
Sugars and amino acids are examples of molecules that move across the plasma membrane using facilitated diffusion. Also, GLUT transporters are a group of carrier proteins that move glucose sugars and associated hexose sugars across the plasma membrane[1].

Carrier proteins

These are proteins that span the plasma membrane. Each protein carrier is specific to bind to a complementary molecule. On one side of the membrane (higher concentration of molecules), the molecules bind to the carrier protein. The carrier then changes conformational shape to release the molecules on the other side of the membrane (where there is a lower concentration of the molecules)[3].

Factors affecting rate of facilitated diffusion

1. Difference in concentration between the two sides of the membrane.
2. The frequency of carrier proteins available on the plasma membrane.
3. The time taken for the molecule to bind with the carrier protein.
4. Type of carrier protein utilized as some carriers are also specific to similar shaped molecules.

[3]

References

  1. 1.0 1.1 1.2 Dee Unglaub Silverthorn (2010). Human Physiology. 5th Edition. Pearson Internation Edition. Page 145-146.
  2. Alberts et al (2002). Molecular Biology of the Cell. 4th Edition. US Garland Science. Page 618.
  3. 3.0 3.1 Barry G. Hinwood (1992). A Textbook of Science for the Health Professions. Nelson Thornes. Page 255-256.