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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B6280 NBQXSummary: AMPA receptor antagonist -
B6282 SKF 97541Summary: GABAB agonist -
B6285 3-Methyl-GABASummary: GABA aminotransferase activator -
B6291 β-CCBSummary: benzodiazepine receptor ligand -
B6295 YS-035 hydrochlorideSummary: inhibitor of outward K+ currents -
B6341 trans-4-Hydroxycrotonic acidSummary: ligand of γ-hydroxybutyric acid (GHB) receptor -
B6381 PPADS tetrasodium saltSummary: P2 purinergic antagonist -
B6386 Synthalin sulfateSummary: NMDA receptor antagonist -
B6394 FGIN-1-27Summary: high affinity agonist of the translocator protein (TSPO,peripheral benzodiazepine receptor) -
B6395 FGIN-1-43Summary: ligand as probe for the mitochondial DBI receptor (peripheral benzodiazepine receptor)
