3D model (JSmol)
|Molar mass||3422 g/mol|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Maitotoxin (or MTX) is an extremely potent toxin produced by Gambierdiscus toxicus, a dinoflagellate species. Maitotoxin is so potent that it has been demonstrated that an intraperitoneal injection of 130 ng/kg was lethal in mice. Maitotoxin was named from the ciguateric fish Ctenochaetus striatus—called "maito" in Tahiti—from which maitotoxin was isolated for the first time. It was later shown that maitotoxin is actually produced by the dinoflagellate Gambierdiscus toxicus.
Mechanism of toxicity
Maitotoxin activates extracellular calcium channels, leading to an increase in levels of cytosolic Ca2+ ions. The exact molecular target of maitotoxin is unknown, but it has been suggested that maitotoxin binds to the plasma membrane Ca2+ ATPase (PMCA) and turn it into an ion channel, similar to how palytoxin turn the Na+/K+-ATPase into an ion channel. Ultimately, a necroptosis cascade is activated, resulting in membrane blebbing and eventually cell lysis. Maitotoxin can indirectly activate calcium-binding proteases calpain-1 and calpain-2, contributing to necrosis. The toxicity of maitotoxin in mice is the highest for nonprotein toxins: the LD50 is 50 ng/kg.
The molecule itself is a system of 32 fused rings. It resembles large fatty acid chains and it is notable because it is one of the largest and most complex non-protein, non-polysaccharide molecules produced by any organism. Maitotoxin includes 32 ether rings, 22 methyl groups, 28 hydroxyl groups, and 2 sulfuric acid esters and has an amphipathic structure. Its structure was established through analysis using nuclear magnetic resonance at Tohoku University, Harvard University and the University of Tokyo in combination with mass spectrometry, and synthetic chemical methods. However, Andrew Gallimore and Jonathan Spencer have questioned the structure of maitotoxin at a single ring-junction (the J–K junction), based purely on biosynthetic considerations and their general model for marine polyether biogenesis. K. C. Nicolaou and Michael Frederick argue that despite this biosynthetic argument, the originally proposed structure could still be correct.  The controversy has yet[needs update] to be resolved.
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- Murata, M; et al. (1994). "Structure and partial stereochemical assignments for maitotoxin, the most toxic and largest natural non-biopolymer". J. Am. Chem. Soc. 116 (16): 7098–7107. doi:10.1021/ja00095a013.
- Sasaki, M; et al. (1996). "The complete structure of maitotoxin, I; Configuration of the C1-C14 side chain". Angew. Chem. Int. Ed. Engl. 35 (15): 1672–1675. doi:10.1002/anie.199616721.
- Kishi, Y (1998). "Complete structure of maitotoxin". Pure Appl. Chem. 70 (2): 339–344. doi:10.1351/pac199870020339.
- Gallimore AR, Spencer JB (2006). "Stereochemical Uniformity in Marine Polyether Ladders—Implications for the Biosynthesis and Structure of Maitotoxin". Angew. Chem. Int. Ed. Engl. 45 (27): 4406–4413. doi:10.1002/anie.200504284. PMID 16767782.
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- Nicolaou, K. C., Cole, Kevin P., Frederick, Michael O., Aversa, Robert J. and Denton, Ross M. (2007), Chemical Synthesis of the GHIJK Ring System and Further Experimental Support for the Originally Assigned Structure of Maitotoxin. Angew. Chem. Int. Ed., 46: 8875–8879. doi:10.1002/anie.200703742
- Chemical Synthesis of the GHIJKLMNO Ring System of Maitotoxin K. C. Nicolaou, Michael O. Frederick, Antonio C. B. Burtoloso, Ross M. Denton, Fatima Rivas, Kevin P. Cole, Robert J. Aversa, Romelo Gibe, Taiki Umezawa, and Takahiro Suzuki Journal of the American Chemical Society 2008 130 (23), 7466-7476 doi:10.1021/ja801139f
- Synthesis of the ABCDEFG Ring System of Maitotoxin K. C. Nicolaou, Robert J. Aversa, Jian Jin, and Fatima Rivas Journal of the American Chemical Society 2010 132 (19), 6855-6861 doi:10.1021/ja102260q
- Synthesis and Biological Evaluation of QRSTUVWXYZA′ Domains of Maitotoxin K. C. Nicolaou, Philipp Heretsch, Tsuyoshi Nakamura, Anna Rudo, Michio Murata, and Keiichi Konoki Journal of the American Chemical Society Article 2014 ASAP doi:10.1021/ja509829e
- Chemistry's toughest total synthesis challenge put on hold by lack of funds Katrina Kramer 15 January 2015 Chemistry World http://www.rsc.org/chemistryworld/2015/01/chemistry-grandest-total-synthesis-challenge-maitotoxin-put-hold-lack-funds