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Psalmotoxin
PDB 1lmm EBI.jpg
Properties
Molecular formula C200H312N62O57S6
Molar mass 4689.39 g mol−1
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Psalmotoxin (PcTx1) is a spider toxin from the venom of the South American tarantula Psalmopoeus cambridgei.[1][2] It can desensitize Acid Sensing Ion Channels (ASIC), which are proton-gated sodium channels.

Contents

Source

Psalmotoxin is a toxin produced in the venom glands of the South American tarantula Psalmopoeus cambridgei.[2]

Chemistry

The psalmotoxin structure can be classified as an inhibitor cysteine knot (ICK) protein. Many ion channel effectors from snail, spider, and scorpion venoms share a similar ICK structure, although they possess very different pharmalogical profiles. Among ICK toxins, psalmotoxin is the only peptide known to act on homomeric ASIC1 channels.[3]

Psalmotoxin is a 40-amino acid peptide, possessing 6 cysteines linked by three disulfide bridges. The three-dimensional structure consists of a compact disulfide-bonded core from which three loops and the N and C termini emerge. The main element of the structure is a three-stranded antiparallel β-sheet.[4]

Target

Psalmopoeus cambridgei, subadult

Psalmotoxin can bind to a particular isoform of the Acid Sensing Ion Channel, the Acid Sensing Ion Channel 1 (ASIC1).[5] The binding of psalmotoxin has an effect on both of the two splice variants known of ASIC1, ASIC1a and ASIC1b.[6] ASIC1 has two transmembrane components. After the first transmembrane component it forms a large extracellular bridge with the second transmembrane component, an extracellular loop. This extracellular loop contains cysteine rich domains. Psalmotoxin specifically binds these cysteine rich domains in the extracellular loop of ASIC1. This implicates this domain is the receptor site of ASIC1 for psalmotoxin.[7]

ASICs are proton-gated sodium channels. ASICs open when H+ binds. This occurs when the H+-concentration in the environment of the neuron is slightly higher compared to resting H+-concentrations (pH = 7.4).[6]

The expression of ASIC1a is high in both the central nervous system and in the sensory neurons of the dorsal root ganglia. ASIC1b is only expressed in sensory neurons. Expression of ASIC1a in the central nervous system relates to the involvement of ASIC1a in higher brain functions, such as learning, memory and fear conditioning.[8] Expression of ASIC1a and ASIC1b in sensory neurons relates to their involvement in nociception[9][10][11][12] and taste.[13]

Mode of action

Binding of psalmotoxin to ASIC1a is reported to increase the affinity of ASIC1a for H+. This increase in affinity for H+ results in the shift of ASIC1a into the desensitized state at resting H+-concentrations (pH = 7.4). The channel being desensitized means that the ion channel is bound to its ligand, H+, but is not able to let ions pass through the ion channel. The underlying mechanism of how this increase in affinity for H+ accounts for a shift of the ASIC1a channels into the desensitized state is not yet specified.[6]

Psalmotoxin also interacts with ASIC1b. In contrast to psalmotoxin binding to ASIC1a, binding of psalmotoxin to ASIC1b results in promoting the opening of the channel. This agonistic effect of psalmotoxin on ASIC1b only occurs in slightly acidic conditions (pH = 7.1).[14]

Toxicity

The role of psalmotoxin in prey capture and the importance of ASIC1a channels as targets of venom components remains unclear.[1]

Therapeutic uses

Psalmotoxin is currently not used for therapeutic purposes, but understanding the psalmotoxin/ASIC1a interaction may be of therapeutic value. Recently, it has been shown that activation of ASIC1a during the acidosis accompanying brain ischemia leads to significant Ca2+ influx, which contributes to neuronal cell death. Inhibition of ASIC1a by psalmotoxin significantly decreased ischemic neuronal cell death. Therefore, it is suggested that desensitized ASIC1's by pharmological intervention could be beneficial for patients at risk of having a stroke.[15] For the same reasons psalmotoxin could contribute in the search for a cure for gliomas.[16] Inhibition of ASIC1a in the amygdala by psalmotoxin could have an anxiolytic effect.[17] As ASIC's play a role in nociception, psalmotoxin could be helpful in designing new analgesic drugs acting directly against pain at the nociceptor level.[2]

References

  1. ^ a b Nicholson, Graham M. (2006). "Spider Venom Peptides". in Kastin, Abba J.. Handbook of biologically active peptides. Academic Press. pp. 369–380 (376). ISBN 978-0-12-369442-3. OCLC 71846806. http://books.google.com/books?id=n8SV9iM6kT0C&pg=PA369. Retrieved 14 October 2009.  
  2. ^ a b c Mazzuca, Michel; Heurteaux, Catherine; Alloui, Abdelkrim; Diochot, Sylvie; Baron, Anne; Voilley, Nicolas; Blondeau, Nicolas; Escoubas, Pierre et al. (2007). "A tarantula peptide against pain via ASIC1a channels and opioid mechanisms". Nature Neuroscience 10: 943. doi:10.1038/nn1940.  
  3. ^ Escoubas, Pierre; Bernard, Cédric; Lambeau, Gérard; Lazdunski, Michel; Darbon, Hervé (2003). "Recombinant production and solution structure of PcTx1, the specific peptide inhibitor of ASIC1a proton-gated cation channels". Protein Science 12 (7): 1332–43. doi:10.1110/ps.0307003. PMID 12824480.  
  4. ^ Escoubas, Pierre; De Weille, Jan R.; Lecoq, Alain; Diochot, Sylvie; Waldmann, Rainer; Champigny, Guy; Moinier, Danielle; Ménez, André et al. (2000). "Isolation of a tarantula toxin specific for a class of proton-gated Na+ channels". The Journal of Biological Chemistry 275 (33): 25116–21. doi:10.1074/jbc.M003643200. PMID 10829030.  
  5. ^ Qadri, Yawar J.; Berdiev, Bakhrom K.; Song, Yuhua; Lippton, Howard L.; Fuller, Catherine M.; Benos, Dale J. (2009). "Psalmotoxin-1 docking to human acid-sensing ion channel-1". The Journal of Biological Chemistry 284 (26): 17625–33. doi:10.1074/jbc.M109.003913. PMID 19395383.  
  6. ^ a b c Chen, Xuanmao; Kalbacher, Hubert; Gründer, Stefan (2005). "The tarantula toxin psalmotoxin 1 inhibits acid-sensing ion channel (ASIC) 1a by increasing its apparent H+ affinity". The Journal of General Physiology 126 (1): 71–9. doi:10.1085/jgp.200509303. PMID 15955877.  
  7. ^ Salinas, Miguel; Rash, Lachlan D.; Baron, Anne; Lambeau, Gérard; Escoubas, Pierre; Lazdunski, Michel (2006). "The receptor site of the spider toxin PcTx1 on the proton-gated cation channel ASIC1a". The Journal of Physiology 570 (Pt 2): 339–54. doi:10.1113/jphysiol.2005.095810. PMID 16284080.  
  8. ^ Wemmie, John A.; Chen, Jianguo; Askwith, Candice C.; Hruska-Hageman, Alesia M.; Price, Margaret P.; Nolan, Brian C.; Yoder, Patrick G.; Lamani, Ejvis et al. (2002). "The acid-activated ion channel ASIC contributes to synaptic plasticity, learning, and memory". Neuron 34 (3): 463–77. doi:10.1016/S0896-6273(02)00661-X. PMID 11988176.  
  9. ^ Sutherland, Stephani P.; Benson, Christopher J.; Adelman, John P.; McCleskey, Edwin W. (2001). "Acid-sensing ion channel 3 matches the acid-gated current in cardiac ischemia-sensing neurons". Proceedings of the National Academy of Sciences of the United States of America 98 (2): 711–6. doi:10.1073/pnas.011404498. PMID 11120882.  
  10. ^ Voilley, Nicolas; de Weille, Jan; Mamet, Julien; Lazdunski, Michel (2001). "Nonsteroid anti-inflammatory drugs inhibit both the activity and the inflammation-induced expression of acid-sensing ion channels in nociceptors". The Journal of Neuroscience 21 (20): 8026–33. PMID 11588175. http://www.jneurosci.org/cgi/content/abstract/21/20/8026.  
  11. ^ Mamet, Julien; Baron, Anne; Lazdunski, Michel; Voilley, Nicolas (2002). "Proinflammatory mediators, stimulators of sensory neuron excitability via the expression of acid-sensing ion channels". The Journal of Neuroscience 22 (24): 10662–70. PMID 12486159. http://www.jneurosci.org/cgi/content/abstract/22/24/10662.  
  12. ^ Chen, Chih-Cheng; Zimmer, Anne; Sun, Wei-Hsin; Hall, Jennifer; Brownstein, Michael J.; Zimmer, Andreas (2002). "A role for ASIC3 in the modulation of high-intensity pain stimuli". Proceedings of the National Academy of Sciences of the United States of America 99 (13): 8992–7. doi:10.1073/pnas.122245999. PMID 12060708.  
  13. ^ Ugawa, Shinya; Yamamoto, Takashi; Ueda, Takashi; Ishida, Yusuke; Inagaki, Akira; Nishigaki, Makoto; Shimada, Shoichi (2003). "Amiloride-insensitive currents of the acid-sensing ion channel-2a (ASIC2a)/ASIC2b heteromeric sour-taste receptor channel". The Journal of Neuroscience 23 (9): 3616–22. PMID 12736332. http://www.jneurosci.org/cgi/content/abstract/23/9/3616.  
  14. ^ Chen, Xuanmao; Kalbacher, Hubert; Gründer, Stefan (2006). "Interaction of Acid-sensing Ion Channel (ASIC) 1 with the Tarantula Toxin Psalmotoxin 1 is State Dependent". The Journal of General Physiology 127 (3): 267–276. doi:10.1085/jgp.200509409. PMID 16505147.  
  15. ^ Xiong, Zhi-Gang; Zhu, Xiao-Man; Chu, Xiang-Ping; Minami, Manabu; Hey, Jessica; Wei, Wen-Li; MacDonald, John F.; Wemmie, John A. et al. (2004). "Neuroprotection in ischemia: blocking calcium-permeable acid-sensing ion channels". Cell 118 (6): 687–98. doi:10.1016/j.cell.2004.08.026. PMID 15369669.  
  16. ^ Ross, Sandra B.; Fuller, Catherine M.; Bubien, James K.; Benos, Dale J. (2007). "Amiloride-sensitive Na+ channels contribute to regulatory volume increases in human glioma cells". American Journal of Physiology. Cell Physiology 293 (3): C1181–5. doi:10.1152/ajpcell.00066.2007. PMID 17615161.  
  17. ^ Dwyer, Jason M.; Sukoff Rizzo, Stacey J.; Neal, Sarah J.; Lin, Qian; Jow, Flora; Arias, Robert L.; Rosenzweig-Lipson, Sharon; Dunlop, John et al. (2009). "Acid sensing ion channel (ASIC) inhibitors exhibit anxiolytic-like activity in preclinical pharmacological models". Psychopharmacology 203 (1): 41–52. doi:10.1007/s00213-008-1373-7. PMID 18949460.  
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