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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B6593 CGP 54626 hydrochlorideSummary: GABAB receptor antagonist -
B6594 8-Bromo-cGMP, sodium saltSummary: cGMP analog that activates protein kinase G (PKG) -
B6599 ATPASummary: GluR5 kainate receptor agonist -
B6602 CGP 37157Summary: Antagonist of mitochondrial Na+-Ca2+ exchanger -
B6604 AM 404Summary: Anandamide transport inhibitor -
B6616 SKF 96365 hydrochloride2 CitationSummary: A potent TRP channel blocker and SOCE inhibitor -
B6629 NF 279Summary: P2X1 antagonist -
B6631 MRS 2219Summary: P2X1 receptor potentiator -
B6639 IDRA 21Summary: Inhibits AMPA receptor desensitization -
B6643 2-APBSummary: antagonist of Ins(1,4,5) P3-induced Ca2+ release

