Open Access Articles- Top Results for Amatoxin


Amatoxins are a subgroup of at least eight toxic compounds found in several genera of poisonous mushrooms, most notably Amanita phalloides and several other members of the genus Amanita, as well as some Conocybe, Galerina and Lepiota mushroom species.


The compounds have a similar structure, that of eight amino-acid residues arranged in a conserved macrobicyclic motif (an overall pentacyclic structure when counting the rings inherent in the proline and tryptophan-derived residues); they were isolated in 1941 by Heinrich O. Wieland and Rudolf Hallermayer.[1] All amatoxins are oligopeptides that are synthesized as 35-amino-acid proproteins, from which the final eight amino acids are cleaved by a prolyl oligopeptidase.[2]

File:Amatoxins generic strucuture.png
The backbone structure (black) is the same in all the amatoxins and five variable groups (red) determine the specific compound.

There are currently ten known amatoxins:[3]

Name R1 R2 R3 R4 R5
α-Amanitin OH OH NH2 OH OH
β-Amanitin OH OH OH OH OH
γ-Amanitin H OH NH2 OH OH
ε-Amanitin H OH OH OH OH
Amanullin H H NH2 OH OH
Amanullinic acid H H OH OH OH
Amaninamide OH OH NH2 H OH
Amanin OH OH OH H OH
Proamanullin H H NH2 OH H

δ-Amanitin has been reported, but its chemical structure has not been determined.


Amatoxins are potent and selective inhibitors of RNA polymerase II, a vital enzyme in the synthesis of messenger RNA (mRNA), microRNA, and small nuclear RNA (snRNA). Without mRNA, which is the template for protein synthesis, cell metabolism stops and lysis ensues.[4] The RNA polymerase of Amanita phalloides is insensitive to the effects of amatoxins; thus, the mushroom does not poison itself.[5]

File:Alpha-Amanitin–RNA polymerase II complex 1K83.png
α-Amanitin (red) bound to RNA polymerase II from Saccharomyces cerevisiae (brewer's yeast). From PDB 1K83.[6]

Shown to the right is the crystal structure of RNA Polymerase II from brewers yeast in complex with the amotoxin alpha-amanatin was captured and solved by Dr. Bushnell et al.,[6] From this crystal structure, it has been determined that alpha-amanitin primarily affects the bridge helix of the RNA pol II complex. The bridge helix is a highly conserved domain of RNA polymerase which is 35 amino acids long. At the N-terminus and the C-terminus of this region there are hinge structures that undergo significant conformational changes throughout the nucleotide addition cycle, and are essential for its progression.[7] One of the many roles of the bridge helix, is facilitating the translocation of DNA. [8] Alpha-amanitin binds to the bridge helix of the RNA Pol II complex and it also binds to part of the complex that is adjacent to the bridge helix, while it is in one specific conformation. This binding locks the bridge helix into place, dramatically slowing its movement in translocating the DNA.[6] The rate of pol II translocation of DNA is reduced from several thousand to a few nucleotides per minute.[9][10]

Symptoms of exposure

Upon exposure to amatoxins, the liver is the principal organ affected as it is the organ which is first encountered after absorption in the gastrointestinal tract. While ingestion is the primary mode of exposure, amatoxins can be absorbed through the skin and also inhaled, thus affecting other organs such as the kidneys and heart, are susceptible. More specifically, exposure to amotoxins may cause irritation of the respiratory tract, headache, dizziness, nausea, shortness of breath, coughing, insomnia, diarrhea, gastrointestinal disturbances, back pain, urinary frequency, liver and kidney damage, or death if ingested or inhaled. For example, If β-amanitin comes in contact with skin, it may cause irritation, burns, redness, severe pain, and could be absorbed through the skin, causing similar effects to exposure via inhalation and ingestion. Contact with the eyes may result in irritation, corneal burns, and eye damage. Persons with pre-existing skin, eye, or central nervous systems disorders, impaired liver, kidney, or pulmonary function may be more susceptible to the effects of this substance. [11]

The estimated minimum lethal dose is 0.1 mg/kg or 7 mg of toxin in adults. Their swift intestinal absorption coupled with their thermostability leads to rapid development of toxic effects in a relatively short period of time. The most severe effects are toxic hepatitis with centrolobular necrosis and hepatic steatosis, as well as acute tubulointerstitial nephropathy, which altogether induce a severe hepatorenal syndrome.

Physiological mechanism of action

Amatoxins are able to travel through the bloodstream to reach the organs in the body. While these compounds can damage many organs, damage to the liver and heart result in fatalities. At the molecular level, amatoxins cause damage to cells of these organs by causing perforations in the plasma membranes resulting in misplaced organelles that are normally in the cytoplasm to be found in the extracellular matrix.[12] beta-Amanitin is also an inhibitor of eukaryotic RNA polymerase II and RNA polymerase III, and as a result, mammalian protein synthesis. It has not been found to inhibit RNA polymerase I or bacterial RNA polymerase.[13] Because it inactivates the RNA polymerases, the liver is unable to repair the damage that beta-amanitin causes and the cells of the liver disintegrate and the liver dissolves.[14]


Treatment involves high dose penicillin as well as supportive care in cases of hepatic and renal injury. Silibinin, a product found in milk thistle, is a potential antidote to amatoxin poisoning, although more data needs to be collected. Cautious attention is given to maintaining hemodynamic stability, although if hepatorenal syndrome has developed the prognosis is guarded at best.[15]


Presence of amatoxins in mushroom samples may be detected by the Meixner Test (also known as the Wieland Test). The amatoxins may be quantitated in plasma or urine using chromatographic techniques to confirm a diagnosis of poisoning in hospitalized patients and in postmortem tissues to aid in a medicolegal investigation of a suspected fatal overdosage.[16]

See also


  1. Litten, W. (March 1975). "The most poisonous mushrooms". Scientific American 232 (3): 90–101. PMID 1114308. doi:10.1038/scientificamerican0375-90. 
  2. H. E. Hallen, H. Luo, J. S. Scott-Craig, and J. D. Walton (2007). "Gene family encoding the major toxins of lethal Amanita mushrooms". Proceedings of the National Academy of Sciences USA 104 (48): 19097–19101. Bibcode:2007PNAS..10419097H. PMC 2141914. PMID 18025465. doi:10.1073/pnas.0707340104. 
  3. K. Baumann, K. Muenter, and H. Faulstich (1993). "Identification of structural features involved in binding of α-amanitin to a monoclonal antibody". Biochemistry 32 (15): 4043–4050. PMID 8471612. doi:10.1021/bi00066a027. 
  4. Karlson-Stiber C, Persson H (2003). "Cytotoxic fungi - an overview". Toxicon 42 (4): 339–49. PMID 14505933. doi:10.1016/S0041-0101(03)00238-1. 
  5. Horgen, Paul A.; Vaisius, Allan C.; Ammirati, Joseph F. (1978). "The insensitivity of mushroom nuclear RNA polymerase activity to inhibition by amatoxins". Archives of Microbiology 118 (3): 317–9. PMID 567964. doi:10.1007/BF00429124. 
  6. 6.0 6.1 6.2 Bushnell, D. A.; Cramer, P; Kornberg, RD (Feb 2002). "Structural basis of transcription: alpha-amanitin-RNA polymerase II cocrystal at 2.8 A resolution". Proc Natl Acad Sci USA 99 (3): 1218–1222. Bibcode:2002PNAS...99.1218B. PMC 122170. PMID 11805306. doi:10.1073/pnas.251664698. 
  7. Weinzierl, R.O.J. (Sep 2011). "The Bridge Helix of RNA Polymerase Acts as a Central Nanomechanical Switchboard for Coordinating Catalysis and Substrate Movement". Archea 2011: 1–7. doi:10.1155/2011/608385. 
  8. Hein, P.P. and Landick, R. (2010). "The bridge helix coordinates the movements of modules in RNA polymerase". BMC Biology 8: 141. doi:10.1186/1741-7007-8-141. 
  9. Chafin, D. R. , Guo, H. & Price, D. H. (1995). "Action of alpha-Amanitin during Pyrophosphorolysis and Elongation by RNA Polymerase II". J. Biol. Chem. 270 (32): 19114–19119. PMID 7642577. doi:10.1074/jbc.270.32.19114. 
  10. Rudd, M. D. & Luse, D. S. (1996). "Amanitin Greatly Reduces the Rate of Transcription by RNA Polymerase II Ternary Complexes but Fails to Inhibit Some Transcript Cleavage Modes". J. Biol. Chem. 271 (35): 21549–21558. PMID 8702941. doi:10.1074/jbc.271.35.21549. 
  11. "Material Safety Data Sheet for beta Amanitin", Retrieved on 12 March 2013.
  12. J. Meldolesi, G. Pelosi, A. Brunelli and E. Genovese (1966). "Electron Microscopic Studies on the Effects of Amanitin in Mice: Liver and Heart Lesions". Virchows Archiv. A, Pathological anatomy and histology 342: 221–235. doi:10.1007/bf00960591. 
  13. "β-Amanitin from Amanita phalloides", Retrieved on 12 March 2013.
  14. "Polypeptide Toxins in Amanita Mushrooms", “Cornell University”, Retrieved on 12 March 2013.
  15. Piqueras J. (1989). "Hepatotoxic mushroom poisoning: diagnosis and management". Mycopathologia 105 (2): 99–110. PMID 2664527. doi:10.1007/bf00444032. 
  16. R. Baselt, Disposition of Toxic Drugs and Chemicals in Man, 8th edition, Biomedical Publications, Foster City, CA, 2008, pp. 52–54.