Anion exchange transporter

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Anion Exchange Transporter[edit | edit source]

The anion exchange transporter (AET) is a type of membrane transport protein that facilitates the movement of anions across a cell membrane. This process is crucial for maintaining the electrochemical gradient within cells, which is essential for various cellular functions such as neuronal signaling and muscle contraction.

Structure and Function[edit | edit source]

Anion exchange transporters are integral membrane proteins that span the lipid bilayer of the cell membrane. They have a specific binding site for anions, which allows them to selectively transport these negatively charged ions in and out of the cell.

The function of an anion exchange transporter is to maintain the balance of anions in the cell. This is achieved by exchanging one type of anion for another. For example, the anion exchange transporter may transport a chloride ion out of the cell in exchange for a bicarbonate ion entering the cell. This process is known as anion exchange.

Types of Anion Exchange Transporters[edit | edit source]

There are several types of anion exchange transporters, each with a specific function and location within the cell. These include:

  • Band 3 protein: This is the most common type of anion exchange transporter and is found in the red blood cell membrane. It is responsible for the exchange of chloride and bicarbonate ions, which is crucial for carbon dioxide transport in the blood.
  • AE2: This transporter is found in the stomach and pancreas, where it helps to regulate the pH of the digestive system by exchanging chloride and bicarbonate ions.
  • AE3: This transporter is found in the heart and brain, where it plays a role in regulating the electrical activity of these organs.

Clinical Significance[edit | edit source]

Mutations in the genes encoding anion exchange transporters can lead to various diseases. For example, mutations in the gene encoding the band 3 protein can cause hereditary spherocytosis, a condition characterized by abnormal red blood cells. Similarly, mutations in the AE2 gene can lead to primary biliary cirrhosis, a disease of the liver.

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References[edit | edit source]

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Contributors: Prab R. Tumpati, MD