Agonists tend to work in favor of something, therefore an agonist for a ligand-gated ion channel would open the channel whereas an antagonist would prevent it from opening.
There are voltage-gated ion channels and ligand-gated ion channels, and since both are stimuli the term stimulus-gated is a redundancy.
A specific molecule binding to it
Voltage-gated ion channels are activated by changes in membrane potential, while ligand-gated ion channels are activated by binding of specific molecules (ligands). Voltage-gated channels open in response to changes in electrical charge across the membrane, whereas ligand-gated channels open when a specific ligand binds to the channel. Additionally, voltage-gated channels are regulated by membrane potential, while ligand-gated channels are regulated by the presence or absence of specific ligands.
Ligand-gated ion channels are activated by binding of specific molecules (ligands) to the channel, while voltage-gated ion channels are activated by changes in the electrical potential across the cell membrane. Ligand-gated channels are regulated by the presence of ligands, while voltage-gated channels are regulated by changes in membrane potential.
Ligand-gated ion channels are activated by binding of specific molecules (ligands) to the channel, while voltage-gated ion channels are activated by changes in the electrical potential across the cell membrane. Ligand-gated channels are regulated by the presence of ligands, while voltage-gated channels are regulated by changes in membrane potential.
It is a carrier protein
ligand-gated or voltage-gated ion channels.
Ionotropic receptors are ligand-gated or transmitter gated ion channels. The binding of a neurotransmitter or other ligand to a particular site on a domain of a protein in the receptor causes a conformational change in the protein subunits. This allows a certain ion to pass through, poteitally potassium, sodium or chloride. There are two types of ionotropic receptors, non-NMDA and NMDA. Both are ligand gated receptors, however the NMDA is also voltage gated.
Voltage-gated ion channels are activated by changes in membrane potential, while ligand-gated ion channels are activated by binding of specific molecules (ligands). Voltage-gated channels open in response to changes in electrical charge across the membrane, whereas ligand-gated channels open when a specific molecule binds to them. Additionally, voltage-gated channels are regulated by membrane potential, while ligand-gated channels are regulated by the presence of specific ligands.
When a ligand-gated channel is stimulated, the specific ligand (or chemical signal) binds to the receptor site on the channel, causing a conformational change in the channel protein. This change opens or closes the channel, allowing specific ions to flow through. This ion movement can generate an electrical signal in the cell and trigger various physiological responses.
A gated channel is a protein channel in a cell membrane that can open or close to allow specific ions, like sodium or potassium, to pass through. The opening and closing of these channels are controlled by certain signals, like changes in voltage or the binding of specific molecules, in order to regulate the flow of ions into and out of the cell.