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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M1062 Taurine and hypotaurinemetabolismSummary: Bile acid derivative, promotes lipid emulsification and absorption, supports lipase-mediated degradation. -
M1080 Aminoadipic acidSummary: An intermediate used to study the metabolic mechanisms of lysine and glucopurine. -
M1133 Indole-2-carboxylic acidSummary: Has lipid peroxidation and competitive NMDA receptor inhibitory activity. -
M1303 caprate (10:0)Summary: A fatty acid with anti-epileptic activity and the ability to inhibit liver cancer cells. -
C8814 Lidocaine hydrochloride hydrateSummary: A research-use reagent for studying local anesthetics and antiarrhythmic agents

