Chloride Ion Channels Alexander Chew Florida State University BSC5936 February 2005.

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Presentation transcript:

Chloride Ion Channels Alexander Chew Florida State University BSC5936 February 2005

Types ELG CFTR –ABC CLC CLNS1A CLIC CLCA Note: Often chloride ion channels are permeable to other anions. Chloride happens to be the most abundant anion.

Functions Regulate cell volume Regulate membrane potential –Resting potential –Depolarization Signal propagation Transport processes

Gating Mechanisms Voltage Volume (swelling) Ligand Binding Ion Concentration Phosphorylation ATP

Some Diseases Associated With Chloride Ion Channels Cystic Fibrosis Genetic disorder Gland secretions are abnormally thick Chloride Ion Channels may be targeted as a treatment for some Respiratory Diseases by regulating abnormal mucus production. –Asthma –COPD (Chronic Obstructive Pulmonary Disease) –Chronic Bronchitis

Myotonia Congenita Genetic neuromuscular disorder Symptoms include muscle stiffness and enlargement

Barter’s Syndrome Covers a group of disorders characterized by defective salt reabsorbing mechanisms

“ The different ways in which ion channels composed of more than one protein can form pores. a, In tetrameric potassium channels, a single pore is formed by four identical or structurally similar proteins (subunits). b, In 'ligand-gated' cation or anion channels (such as channels that detect the neurotransmitters acetylcholine or GABA), the single pore is formed by five identical or structurally similar subunits. c, Chloride channels from the CLC family are dimers, in which each subunit has its own pore. d, Aquaporin water channels are tetramers, again with one pore per subunit. ”

“ Chloride-channel structure, as revealed by Dutzler et al. 2. This is a side-on view of one of the two subunits of a CLC channel, looking at the side that interacts with the other subunit. -Helical structures are indicated by cylinders, coloured in green and cyan to indicate the two 'repeated' units. Regions directly involved in formation of the ion-permeation pore are in red. A negative charge that might be involved in gating the channel is shown as a green circle; it is just above where the chloride ion (shown in yellow) is coordinated. The amino terminus of helix R (bright blue) contains a tyrosine amino acid, which helps to coordinate the Cl - ion; the carboxy terminus emerges into the cell. In mammalian CLCs, helix R is connected to a large intracellular region, indicated by the dashed line. ” fig_tab/415276a_F2.html

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