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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B6823 Cl-HIBOSummary: desensitising AMPA receptor agonist -
B6832 SCH 28080Summary: H+,K+-ATPase inhibitor -
B6840 CL 218872Summary: Benzodiazepine agonist -
B6849 UBP 282Summary: AMPA and kainate receptor antagonist -
B6850 UBP 301Summary: kainate receptor antagonist -
B6854 NNC 711Summary: GABA uptake inhibitor -
B6862 E-4031 dihydrochlorideSummary: A Kv11.1 (hERG) K+ channel blocker -
B6866 N-ArachidonylGABASummary: arachidonyl amino acid -
B6880 MRS 1845Summary: store-operated Ca2+ channels blocker -
B6901 UCM 707Summary: endocannabinoid transport inhibitor

