Sandbox Reserved 996

Ectatomin (1eci)

spinqualitylabelsall models 1eci, 20 NMR models Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Ectatomin (1eci) is the main component of venom of the ant Ectatomma tuberculatum, making up 15%-18% of the crude venom and accounting for 90% of the venom's toxicity. When bitten by E. tuberculatum, Ectatomin inserts into the target's cell membranes and forms a nonselective cation channel. The calculated isoelectric point and molecular weight of Ectatomin are 9.95 and 7928 Da, respectively. Structure Biologically, Ectatomin exists as a heterodimer stabilized by disulfide linkages linkages. The α subunit has 37 amino acid residues, while the β subunit has 34 amino acid residues. The structure of Ectatomin was solved using 2D NMR and CHARMm computational optimization, though there are 20 similar proposed models in total. Generally, each subunit is composed of two antiparallel α-helices, linked by disulfide bonds, with a connecting hairpin hinge region. The two subunits are linked by a disfulide bond between their hairpin hinge regions. One α-helix from each subunit is kinked approximately 40°, due to the presence of proline residues. The kinked α-helix of the α subunit is more kinked, containing three proline residues, while the kinked α-helix of the β subunit only contains one proline residue. The internal region between the two subunits is primarily composed of hydrophobic residues. Sequence - α subunit - GVIPKKIWETVCPTVEPWAKKCSGDIATYIKRECGKL Sequence - β subunit - WSTIVKLTICPTLKSMAKKCEGSIATMIKKKCDK Mechanism A proposed insertion (above) and dimerization mechanism to form cation channel (below) of Ectatomin in the cell membrane (gray). Insertion occurs when the α and β subunits open at the hairpin hinge region (shown in black with yellow disulfide bonds), exposing internal hydrophobic residues which interact with hydrophobic lipid tails of the cell membrane. Pore formation occurs after dimerization, allowing ions to freely cross the membrane. Ectatomin has several proposed mechanisms of action. The primary proposed mechanism involves the formation of a nonselective cation channel. In this mechanism, the α and β subunits open up, exposing the internal hydrophobic residues. The protein flattens while remaining attached at the hairpin hinge region. The now exposed hydrophobic residues nonselectively insert into plasma membranes. The inserted protein dimerizes, eventually forming a nonselective cation channel. For the second and third proposed mechanisms of action, Ectatomin has also been shown to inhibit kinases, specifically protein tyrosine kinase and protein kinase C, and Ca2+ channels. Kinase inhibition would potentially allow Ectatomin to interfere with various components of signal transduction. Calcium channel inhibition would potentially allow Ectatomin to affect physiological processes such as contraction, neurotransmitter release and neuronal activity regulation. Toxicology With an LD50 of 6.8 μg kg-1, Ectatomin is one of the deadliest proteins known to man, alongside Tetanospasmin and the Botulinum toxin. Ectatomin attacks and forms pores in the plasma membrane, allowing cations to freely move in and out of the cell. The primary cations which flow through the pore are Ca2+ and K+. . As the concentrations on either side of the cell reach equilibrium, the cells and the person effected with the toxin dies. The major cations effected is the calcium ion. Without the calcium gradient the muscles are not able to contract leaving the effected person paralyzed. Another major worry with free flowing cations reaching equilibrium is with potassium. Without a potassium gradient the heart will not be able to contract/beat leaving the person unable to push oxygen and nutrients throughout the body and to the brain.