Nerve agents and acetylcholinesterase

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<StructureSection load='1eea' size='340' side='right' caption='Caption for this structure' scene=''>
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<StructureSection load='1eea' size='340' side='right' caption='Electric eel acetylcholinesterase (PDB code [[1eea]])' scene=''>
== '''Background''' ==
== '''Background''' ==
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== '''What is Acetylcholine and its Enzyme''' ==
== '''What is Acetylcholine and its Enzyme''' ==
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<scene name='81/814054/Entire_molecule/6'>Acetylcholinesterase</scene> is one of the most efficient human enzymes that is known. It can hydrolyze around 600,000 <scene name='81/814054/Acetylcholinesterase_acetylcho/2'>acetylcholine</scene> molecules each minute which shows how essential it is to human life. <ref name="Stone"> Stone, R. (2018, September 25). How to defeat a nerve agent. Retrieved from https://www.sciencemag.org/news/2018/01/how-defeat-nerve-agent. </ref> Acetylcholinesterase has 3 active sites, according to current research, but nerve agents attack the primary site. The <scene name='81/814054/Active_site_with_surface/1'>gorge</scene> that is located on the molecule near the <scene name='81/814054/Active_site_redone_again/3'>active site</scene> plays an essential role in the function of acetylcholine. <ref name="Xu">Xu, Y., Cheng, S., Sussman, J., Silman, I., & Jiang, H. (2017). Computational Studies on Acetylcholinesterases. Molecules, 22(8), 1324. doi:10.3390/molecules22081324</ref> The active site contains a catalytic triad of histidine, serine, and glutamic acid. The gorge allows the active site to open and close in order to control the flow of substrates that come to acetylcholine. Acetylcholinesterase was found to have 14 aromatic amino acids located around the opening to the gorge and this plays a role in the dipole moment within the molecule and it leads to a more symmetric charge distribution within the molecule. In 2017, it was found that acetylcholinesterase was a very effective catalyst and when a substrate interacts with an enzyme, that becomes the rate-limiting step. <ref name="Xu">Xu, Y., Cheng, S., Sussman, J., Silman, I., & Jiang, H. (2017). Computational Studies on Acetylcholinesterases. Molecules, 22(8), 1324. doi:10.3390/molecules22081324</ref>
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<scene name='81/814054/Entire_molecule/6'>Acetylcholinesterase</scene> is one of the most efficient human enzymes that is known. It can hydrolyze around 600,000 <scene name='81/814054/Acetylcholinesterase_acetylcho/2'>acetylcholine</scene> molecules each minute which shows how essential it is to human life. <ref name="Stone"> Stone, R. (2018, September 25). How to defeat a nerve agent. Retrieved from https://www.sciencemag.org/news/2018/01/how-defeat-nerve-agent. </ref> Acetylcholinesterase has 3 active sites, according to current research, but nerve agents attack the primary site. The <scene name='81/814054/Active_site_with_surface/1'>gorge</scene> that is located on the molecule near the <scene name='81/814054/Active_site_redone_again/4'>active site</scene> plays an essential role in the function of acetylcholine. <ref name="Xu">Xu, Y., Cheng, S., Sussman, J., Silman, I., & Jiang, H. (2017). Computational Studies on Acetylcholinesterases. Molecules, 22(8), 1324. doi:10.3390/molecules22081324</ref> The active site contains a catalytic triad of histidine, serine, and glutamic acid. The gorge allows the active site to open and close in order to control the flow of substrates that come to acetylcholine. Acetylcholinesterase was found to have 14 aromatic amino acids located around the opening to the gorge and this plays a role in the dipole moment within the molecule and it leads to a more symmetric charge distribution within the molecule. In 2017, it was found that acetylcholinesterase was a very effective catalyst and when a substrate interacts with an enzyme, that becomes the rate-limiting step. <ref name="Xu">Xu, Y., Cheng, S., Sussman, J., Silman, I., & Jiang, H. (2017). Computational Studies on Acetylcholinesterases. Molecules, 22(8), 1324. doi:10.3390/molecules22081324</ref>
== '''Parts of Nerve Agents''' ==
== '''Parts of Nerve Agents''' ==
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== '''Conclusions''' ==
== '''Conclusions''' ==
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While the chemical structures of some of these nerve agents are not known due to the synthesis of these chemicals being illegal, there are proposed structures since researchers know the essential chemical groups that are a part of nerve agents. Due to the unknown structures, it is difficult to synthesize antidotes to these nerve agents, but researchers can try to find treatments that will work without knowing the structure. The threat of a nerve agent attack is a possibility in our world today and so it is essential to understand how these agents affect the body so that measures can be taken to keep the public as safe as possible.
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While the chemical structures of some of these nerve agents are not known, due to the synthesis of these chemicals being illegal, there are proposed structures. This is because researchers know the essential chemical groups that are a part of nerve agents. Without the structures, it is difficult to synthesize antidotes to these nerve agents, but researchers can try to find treatments that will work based on what is known about how the chemicals interact in the body and the components of nerve agents. The threat of a nerve agent attack is a possibility in our world today and so it is essential to understand how these agents affect the body so that measures can be taken to keep the public as safe as possible.

Current revision

Electric eel acetylcholinesterase (PDB code 1eea)

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References

  1. 1.0 1.1 1.2 Atchison, W. (2018, September 13). What is Novichok? A neurotoxicologist explains. Retrieved from http://theconversation.com/what-is-novichok-a-neurotoxicologist-explains-99736
  2. 2.0 2.1 Cotton, S. (2018). Nerve Agents: What Are They and How Do They Work? American Scientist, 106(3), may/june 2018, 138. doi:10.1511/2018.106.3.138
  3. 3.0 3.1 May, P. (2018, August). Novichok. Retrieved from http://www.chm.bris.ac.uk/motm/novichok/novichokh.htm
  4. 4.0 4.1 4.2 4.3 Gardiner, B. (n.d.). The Chemical Weapons Detectives. Popular Science, 290(5), winter 2018, 88.
  5. 5.0 5.1 Kloske, M., & Witkiewicz, Z. (2019). Novichoks – The A group of organophosphorus chemical warfare agents. Chemosphere, 221, 673. doi:10.1016/j.chemosphere.2019.01.054
  6. 6.0 6.1 6.2 6.3 Stone, R. (2018, September 25). How to defeat a nerve agent. Retrieved from https://www.sciencemag.org/news/2018/01/how-defeat-nerve-agent.
  7. 7.0 7.1 Xu, Y., Cheng, S., Sussman, J., Silman, I., & Jiang, H. (2017). Computational Studies on Acetylcholinesterases. Molecules, 22(8), 1324. doi:10.3390/molecules22081324
  8. Allgardsson, A., Berg, L., Akfur, C., Hörnberg, A., Worek, F., Linusson, A., & Ekström, F. J. (2016). Structure of a prereaction complex between the nerve agent sarin, its biological target acetylcholinesterase, and the antidote HI-6. Proceedings of the National Academy of Sciences, 113(20), 5516. doi:10.1073/pnas.1523362113
  9. Nerve Agents Guide. (n.d.). Retrieved from https://www.osha.gov/SLTC/emergencypreparedness/guides/nerve.html

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