Membrane Transporter/Ion Channel


Membrane Transporters mediate the movement of ions and molecules via binding and moving the substance across the membrane. There are two main actions of transporter: facilitated diffusion (passive transport) and active transport. Membrane transporters which bind the hydrolysis of ATP to the transport of target molecules are referred to as ATPases. For instance, Na+,K+-ATPases or Na+,K+-pumps are responsible for the transport of Na+ out of and K+ into cells.
Ion channels are pore-forming membrane proteins which allow the flow of ions across the membrane. The ion channels can be broadly grouped into six families including calcium channels, chloride channels, potassium channels, sodium channels, gap junction proteins and porins. Not all ion channels are gated, such as certain type of K+ and Cl– channels, transient receptor potential superfamily of cation channels, the ryanodine receptors and the IP3 receptors, but most Na+, K+, Ca2+ and some Cl– channels are all gated by voltage. Ligand-gated channels are regulated in response to ligand binding (e.g. neurotransmitters signaling). These ligand-gated neurotransmitter receptors are known as ionotropic receptors. Various neurotransmitters couple to ionotropic receptors such as glutamate, acetylcholine, glycine, GABA, and serotonin.
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B6677 CI 966 hydrochlorideSummary: GABA transporter GAT-1 inhibitor -
B6682 PPNDSSummary: P2X1 receptor antagonist -
B6692 L-655,708Summary: inverse agonist for the benzodiazepine site of GABAA receptors containing the α5 subunit -
B6700 P1075Summary: Kir6 (KATP) channel opener -
B6711 CromakalimSummary: Kir6 (KATP) channel opener -
B6712 LevcromakalimSummary: prototypical Kir6 (KATP) channel opener -
B6716 NF 449Summary: purinergic receptor antagonist -
B6717 VDM 11Summary: anandamide transport inhibitor -
B6721 CP 339818 hydrochlorideSummary: KV1.3 channel antagonist -
B6723 FPL 64176Summary: L-type Ca2+ channels activator

