Chemistry:Methionine sulfoximine
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| Names | |
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| IUPAC name
(2S)-2-Amino-4-(S-methylsulfonimidoyl)butanoic acid
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| Other names
l-Methionine sulfoximine; MSO
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| Identifiers | |
3D model (JSmol)
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| 1725509 | |
| ChEBI | |
| ChemSpider | |
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PubChem CID
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| UNII | |
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| Properties | |
| C5H12N2O3S | |
| Molar mass | 180.22 g·mol−1 |
| Related compounds | |
Related compounds
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Buthionine sulfoximine Glufosinate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Methionine sulfoximine (MSO, also known as MetSox[1]) is an irreversible glutamine synthetase inhibitor. It is the sulfoximine derivative of methionine with convulsant effects.[2]
Methionine sulfoximine is composed of two different diastereomers, which are L-S-Methionine sulfoximine and L-R-Methionine sulfoximine. These affect the longevity of the model mouse for Lou Gehrig's disease.[3] Overproduction of glutamate results to excitotoxicity, which kills the cell. Since methionine sulfoximine inhibits glutamate production in the brain, it prevents excitotoxicity. Thus, increasing the longevity of the mice.[4]
Mechanism of action
MSO is phosphorylated by glutamine synthetase. The resulting product acts as a transition state analog that is unable to diffuse from the active site, thereby inhibiting the enzyme.[5]
References
- ↑ Carroll, P.; Waddell, S. J.; Butcher, P. D.; Parish, T. (2011). "Methionine sulfoximine resistance in Mycobacterium tuberculosis is due to a single nucleotide deletion resulting in increased expression of the major glutamine synthetase, GlnA1". Microbial Drug Resistance 17 (3): 351–355. doi:10.1089/mdr.2010.0125. PMID 21875360.
- ↑ Rowe, WB; Meister, A (June 1970). "Identification of L-methionine-S-sulfoximine as the convulsant isomer of methionine sulfoximine.". Proceedings of the National Academy of Sciences of the United States of America 66 (2): 500–6. doi:10.1073/pnas.66.2.500. PMID 4393740. Bibcode: 1970PNAS...66..500R.
- ↑ Brusilow, William S. A. (2017-04-24). "Identification of the isomer of methionine sulfoximine that extends the lifespan of the SOD1 G93A mouse". Neuroscience Letters 647: 165–167. doi:10.1016/j.neulet.2017.03.029. ISSN 0304-3940. PMID 28323087.
- ↑ Bame, Monica; Pentiak, Patricia A.; Needleman, Richard; Brusilow, William S. A. (2012-12-01). "Effect of Sex on Lifespan, Disease Progression, and the Response to Methionine Sulfoximine in the SOD1 G93A Mouse Model for ALS". Gender Medicine 9 (6): 524–535. doi:10.1016/j.genm.2012.10.014. ISSN 1550-8579. PMID 23217569.
- ↑ Krajewski, W. W.; Jones, T. A.; Mowbray, S. L. (18 July 2005). "Structure of Mycobacterium tuberculosis glutamine synthetase in complex with a transition-state mimic provides functional insights". Proceedings of the National Academy of Sciences 102 (30): 10499–10504. doi:10.1073/pnas.0502248102. PMID 16027359. Bibcode: 2005PNAS..10210499K.
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