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.
-
B5093 α-Conotoxin MIISummary: antagonist for α3β2 subunit-containing nicotinic receptors -
B5134 L-R4W2Summary: Vanilloid TRPV1 (VR1) receptor antagonist peptide -
B5143 Pep1-TGLSummary: Peptide containing the 'TGL' motif that corresponds to the C-terminus of GluR1 subunit -
B5144 Pep1-AGLSummary: Analog of Pep1-TGL -
B5165 Ionomycin calcium saltSummary: ionophore -
B5258 CALP1Summary: Cell-permeable calmodulin (CaM) agonist -
B5271 PDZ1 Domain inhibitor peptideSummary: Novel cyclic peptide that disrupts interaction between GluR6 and PSD-95 -
B5276 MNI-caged-NMDASummary: NMDA caged with the photosensitive 4-methoxy-7-nitroindolinyl group -
B5289 CALP2Summary: Cell-permeable calmodulin (CaM) antagonist -
B5291 CALP3Summary: Cell-permeable calmodulin (CaM) agonist

