Apamin, Inhibitor of small conductance Ca2+-activated K+ channels
Apamin is a neurotoxin that was originally isolated from Apis mellifera. Apamin binds to and inhibits the SK channels (small conductance Ca2+-activated K+ channels) in the brain and spinal cord. Apamin inhibits three subtypes of SK channels (KCa2.1, KCa2.2, and KCa2.3) with different affinity. Apamin does not affect KCa3.1 channel activity. Apamin most likely acts as a pore blocker such as Scyllatoxin or Tamapin, although residues both inside and outside of the pore region of the SK channels participate in apamin binding. The SK channels are present in a wide range of excitable and non-excitable cells, including cells in the central nervous system, intestinal myocytes, endothelial cells, and hepatocytes.
Apamin technical information
AA sequence: H-Cys1-Asn-Cys3-Lys-Ala-Pro-Glu-Thr-Ala-Leu-Cys11-Ala-Arg-Arg-Cys15-Gln-Gln-His-NH2
Disulfide bonds: Cys1-Cys11 and Cys3-Cys15
Length (aa): 18
Formula: C79H131N31O24S4
Molecular Weight: 2027.34 Da
Appearance: White lyophilized solid
Solubility: water and saline buffer
CAS number: [24345-16-2]
Source: Synthetic
Purity rate: > 98 %
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