Page last updated: 2024-10-24

voltage-gated chloride channel activity

Definition

Target type: molecularfunction

Enables the transmembrane transfer of a chloride ion by a voltage-gated channel. A voltage-gated channel is a channel whose open state is dependent on the voltage across the membrane in which it is embedded. [GOC:mtg_transport, ISBN:0815340729]

Voltage-gated chloride channel activity is a molecular function that describes the ability of a protein to act as a channel for the selective passage of chloride ions (Cl-) across a cell membrane in response to changes in membrane potential. This function is critical for a wide range of physiological processes, including neuronal excitability, muscle contraction, and cell volume regulation.

Here's a detailed breakdown of the process:

1. **Membrane Potential:** Cell membranes maintain an electrical potential difference across them, known as the membrane potential. This potential is typically negative inside the cell compared to the outside.

2. **Voltage Sensing:** Voltage-gated chloride channels are embedded in the cell membrane and contain a voltage-sensing domain. This domain is sensitive to changes in the membrane potential.

3. **Channel Opening:** When the membrane potential reaches a specific threshold, the voltage-sensing domain undergoes a conformational change, opening the channel pore.

4. **Chloride Ion Flow:** The opened channel pore allows chloride ions to flow across the membrane, driven by their electrochemical gradient. This flow of ions can either depolarize or hyperpolarize the membrane, depending on the direction of the ion movement.

5. **Channel Closing:** As the membrane potential returns to its resting state, the voltage-sensing domain reverts to its closed conformation, closing the channel pore.

6. **Regulation:** The activity of voltage-gated chloride channels is tightly regulated by a variety of factors, including membrane potential, intracellular signaling pathways, and binding of specific ligands.

The precise role of voltage-gated chloride channels in different cell types can vary depending on the specific channel subtype expressed. For example, in neurons, these channels contribute to the regulation of neuronal excitability by influencing the timing and duration of action potentials. In muscle cells, they play a role in muscle contraction by mediating the release of calcium ions. In other cell types, they contribute to cell volume regulation, by controlling the movement of water and electrolytes.

In summary, voltage-gated chloride channel activity is a crucial molecular function that enables the selective passage of chloride ions across cell membranes in response to changes in membrane potential. This function is fundamental to many physiological processes, including neuronal excitability, muscle contraction, and cell volume regulation.'
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Proteins (1)

ProteinDefinitionTaxonomy
Anoctamin-1An anoctamin-1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:Q5XXA6]Homo sapiens (human)

Compounds (4)

CompoundDefinitionClassesRoles
niclosamideniclosamide : A secondary carboxamide resulting from the formal condensation of the carboxy group of 5-chlorosalicylic acid with the amino group of 2-chloro-4-nitroaniline. It is an oral anthelmintic drug approved for use against tapeworm infections.

Niclosamide: An antihelmintic that is active against most tapeworms. (From Martindale, The Extra Pharmacopoeia, 30th ed, p48)
benzamides;
C-nitro compound;
monochlorobenzenes;
salicylanilides;
secondary carboxamide
anthelminthic drug;
anticoronaviral agent;
antiparasitic agent;
apoptosis inducer;
molluscicide;
piscicide;
STAT3 inhibitor
nitazoxanidenitazoxanide: a 5-nitrothiazolyl derivative used for a broad range of intestinal parasitic infections including CRYPTOSPORIDIUM and GIARDIA; it is a redox-active nitrothiazolyl-salicylamide prodrugbenzamides;
carboxylic ester
n-((4-methoxy)-2-naphthyl)-5-nitroanthranilic acidN-((4-methoxy)-2-naphthyl)-5-nitroanthranilic acid: inhibits anoctamin-1; structure in first source
t16ainh-a01T16AInh-A01: a TMEM16A inhibitor