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Glutamate–cysteine ligase

April 10, 2024

Glutamate–cysteine ligase (GCL) EC 6.3.2.2), previously known as γ-glutamylcysteine synthetase (GCS), is the first enzyme of the cellular glutathione (GSH) biosynthetic pathway that catalyzes the chemical reaction:

Glutamate–cysteine ligase
Identifiers
EC no.6.3.2.2
CAS no.9023-64-7
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum
Gene OntologyAmiGO / QuickGO
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PMCarticles
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NCBIproteins

L-glutamate + L-cysteine + ATP γ-glutamyl cysteine + ADP + Pi

GSH, and by extension GCL, is critical to cell survival. Nearly every eukaryotic cell, from plants to yeast to humans, expresses a form of the GCL protein for the purpose of synthesizing GSH. To further highlight the critical nature of this enzyme, genetic knockdown of GCL results in embryonic lethality.[1] Furthermore, dysregulation of GCL enzymatic function and activity is known to be involved in the vast majority of human diseases, such as diabetes, Parkinson's disease, Alzheimer's disease, COPD, HIV/AIDS, and cancer.[2][3] This typically involves impaired function leading to decreased GSH biosynthesis, reduced cellular antioxidant capacity, and the induction of oxidative stress. However, in cancer, GCL expression and activity is enhanced, which serves to both support the high level of cell proliferation and confer resistance to many chemotherapeutic agents.[4]

Function edit

Glutamate cysteine ligase (GCL) catalyzes the first and rate-limiting step in the production of the cellular antioxidant glutathione (GSH), involving the ATP-dependent condensation of cysteine and glutamate to form the dipeptide gamma-glutamylcysteine (γ-GC).[5] This peptide coupling is unique in that it occurs between the amino moiety of the cysteine and the terminal carboxylic acid of the glutamate side chain (hence the name gamma-glutamyl cysteine).[6] This peptide bond is resistant to cleavage by cellular peptidases and requires a specialized enzyme, gamma-glutamyl transpeptidase (γGT), to metabolize γ-GC and GSH into its constituent amino acids.[7]

GCL enzymatic activity generally dictates cellular GSH levels and GSH biosynthetic capacity. GCL enzymatic activity is influenced by numerous factors, including cellular expression of the GCL subunit proteins, access to substrates (cysteine is typically limiting in the production of γ-GC), the degree of negative feedback inhibition by GSH, and functionally relevant post-translational modifications to specific sites on the GCL subunits.[8][9][10] Given its status as the rate-limiting enzyme in GSH biosynthesis, changes in GCL activity directly equate to changes in cellular GSH biosynthetic capacity.[11] Therefore, therapeutic strategies to alter GSH production have focused on this enzyme.[12]

Regulation edit

In keeping with its critical importance in maintaining life, GCL is subject to a multi-level regulation of its expression, function, and activity. GCL expression is regulated at the transcriptional (transcription of the GCLC and GCLM DNA to make mRNA), posttranscriptional (the stability of the mRNA over time), translational (processing of the mRNA into protein), and posttranslational levels (involving modifications to the existing proteins).[13][14][15][16] Although baseline constitutive expression is required to maintain cell viability, expression of the GCL subunits is also inducible in response to oxidative stress, GSH depletion, and exposure to toxic chemicals, with the Nrf2, AP-1, and NF-κB transcription factors regulating the inducible and constitutive expression of both subunits[17][18]

In terms of enzyme functional regulation, GSH itself acts as a feedback inhibitor of GCL activity. Under normal physiologic substrate concentrations, the GCLC monomer alone may synthesize gamma-glutamylcysteine; however, the normal physiologic levels of GSH (estimated at around 5 mM) far exceeds the GSH Ki for GCLC,[19] suggesting that only the GCL holoenzyme is functional under baseline conditions. However, during oxidative stress or toxic insults that can result in the depletion of cellular GSH or its oxidation to glutathione disulfide (GSSG), the function of any monomeric GCLC in the cell is likely to become quite important. In support of this hypothesis, mice lacking expression of the GCLM subunit due to genetic knockdown exhibit low levels of tissue GSH (~10–20% of the normal level), which is roughly the level of the GSH Ki for monomeric GCLC.[20][21]

Structure edit

Animal glutamate–cysteine ligase edit

Animal glutamate cysteine ligase (GCL) is a heterodimeric enzyme composed of two protein subunits that are coded by independent genes located on separate chromosomes:

  • Glutamate cysteine ligase catalytic subunit (GCLC, ~73 kDa) possesses all of substrate and cofactor binding sites and is responsible for all of the catalysis.
  • Glutamate cysteine ligase modifier subunit (GCLM, ~31 kDa) has no enzymatic activity on its own but increases the catalytic efficiency of GCLC when complexed in the holoenzyme.

In the majority of cells and tissues, the expression of GCLM protein is lower than GCLC and GCLM is therefore limiting in the formation of the holoenzyme complex. Thus, the sum total of cellular GCL activity is equal to the activity of the holoenzyme + the activity of the remaining monomeric GCLC. composed of a catalytic and a modulatory subunit. The catalytic subunit is necessary and sufficient for all GCL enzymatic activity, whereas the modulatory subunit increases the catalytic efficiency of the enzyme. Mice lacking the catalytic subunit (i.e., lacking all de novo GSH synthesis) die before birth.[22] Mice lacking the modulatory subunit demonstrate no obvious phenotype, but exhibit marked decrease in GSH and increased sensitivity to toxic insults.[23][24][25]

Plant glutamate cysteine ligase edit

The plant glutamate cysteine ligase is a redox-sensitive homodimeric enzyme, conserved in the plant kingdom.[26] In an oxidizing environment, intermolecular disulfide bridges are formed and the enzyme switches to the dimeric active state. The midpoint potential of the critical cysteine pair is -318 mV. In addition to the redox-dependent control, the plant GCL enzyme is feedback inhibited by glutathione.[27] GCL is exclusively located in plastids, and glutathione synthetase (GS) is dual-targeted to plastids and cytosol, thus GSH and gamma-glutamylcysteine are exported from the plastids.[28] Studies also shown that restricting GCL activity to the cytosol or glutathione biosynthesis to the plastids is sufficient for normal plant development and stress tolerance.[29] Both glutathione biosynthesis enzymes are essential in plants; knock-outs of GCL and GS are lethal to embryo and seedling, respectively.[30]

As of late 2007, six structures have been solved for this class of enzymes, with PDB accession codes 1V4G, 1VA6, 2D32, 2D33, 2GWC, and 2GWD.

References edit

  1. ^ Dalton TP, et al. (2004). "Genetically altered mice to evaluate glutathione homeostasis in health and disease". Free Radic Biol Med. 37 (10): 1511–26. doi:10.1016/j.freeradbiomed.2004.06.040. PMID 15477003.
  2. ^ Lu SC (2009). "Regulation of glutathione synthesis". Mol Aspects Med. 30 (1–2): 42–59. doi:10.1016/j.mam.2008.05.005. PMC 2704241. PMID 18601945.
  3. ^ Franklin CC, et al. (2009). "Structure, function, and post-translational regulation of the catalytic and modifier subunits of glutamate cysteine ligase". Mol Aspects Med. 30 (1–2): 86–98. doi:10.1016/j.mam.2008.08.009. PMC 2714364. PMID 18812186.
  4. ^ Backos DS, et al. (2012). "The role of glutathione in brain tumor drug resistance". Biochem Pharmacol. 83 (8): 1005–12. doi:10.1016/j.bcp.2011.11.016. PMID 22138445.
  5. ^ Franklin CC, et al. (2009). "Structure, function, and post-translational regulation of the catalytic and modifier subunits of glutamate cysteine ligase". Mol Aspects Med. 30 (1–2): 86–98. doi:10.1016/j.mam.2008.08.009. PMC 2714364. PMID 18812186.
  6. ^ Njålsson R, Norgren S (2005). "Physiological and pathological aspects of GSH metabolism". Acta Paediatr. 94 (2): 132–137. doi:10.1080/08035250410025285. PMID 15981742.
  7. ^ Lu SC (2009). "Regulation of glutathione synthesis". Mol Aspects Med. 30 (1–2): 42–59. doi:10.1016/j.mam.2008.05.005. PMC 2704241. PMID 18601945.
  8. ^ Backos DS, et al. (2010). "Manipulation of cellular GSH biosynthetic capacity via TAT-mediated protein transduction of wild-type or a dominant-negative mutant of glutamate cysteine ligase alters cell sensitivity to oxidant-induced cytotoxicity". Toxicol Appl Pharmacol. 243 (1): 35–45. doi:10.1016/j.taap.2009.11.010. PMC 2819613. PMID 19914271.
  9. ^ Backos DS, et al. (2011). "Posttranslational modification and regulation of glutamate-cysteine ligase by the α,β-unsaturated aldehyde 4-hydroxy-2-nonenal". Free Radic Biol Med. 50 (1): 14–26. doi:10.1016/j.freeradbiomed.2010.10.694. PMC 3014730. PMID 20970495.
  10. ^ Backos DS, et al. (2013). "Glycation of glutamate cysteine ligase by 2-deoxy-d-ribose and its potential impact on chemoresistance in glioblastoma". Neurochem Res. 38 (9): 1838–49. doi:10.1007/s11064-013-1090-4. PMID 23743623. S2CID 7738579.
  11. ^ Franklin CC, et al. (2009). "Structure, function, and post-translational regulation of the catalytic and modifier subunits of glutamate cysteine ligase". Mol Aspects Med. 30 (1–2): 86–98. doi:10.1016/j.mam.2008.08.009. PMC 2714364. PMID 18812186.
  12. ^ Griffith OW, Meister A (1979). "Potent and specific inhibition of glutathione synthesis by buthionine sulfoximine (S-n-butyl homocysteine sulfoximine)". J Biol Chem. 254 (16): 7558–60. doi:10.1016/S0021-9258(18)35980-5. PMID 38242.
  13. ^ Lu SC (2009). "Regulation of glutathione synthesis". Mol Aspects Med. 30 (1–2): 42–59. doi:10.1016/j.mam.2008.05.005. PMC 2704241. PMID 18601945.
  14. ^ Franklin CC, et al. (2009). "Structure, function, and post-translational regulation of the catalytic and modifier subunits of glutamate cysteine ligase". Mol Aspects Med. 30 (1–2): 86–98. doi:10.1016/j.mam.2008.08.009. PMC 2714364. PMID 18812186.
  15. ^ Backos DS, et al. (2011). "Posttranslational modification and regulation of glutamate-cysteine ligase by the α,β-unsaturated aldehyde 4-hydroxy-2-nonenal". Free Radic Biol Med. 50 (1): 14–26. doi:10.1016/j.freeradbiomed.2010.10.694. PMC 3014730. PMID 20970495.
  16. ^ Backos DS, et al. (2013). "Glycation of glutamate cysteine ligase by 2-deoxy-d-ribose and its potential impact on chemoresistance in glioblastoma". Neurochem Res. 38 (9): 1838–49. doi:10.1007/s11064-013-1090-4. PMID 23743623. S2CID 7738579.
  17. ^ Lu SC (2009). "Regulation of glutathione synthesis". Mol Aspects Med. 30 (1–2): 42–59. doi:10.1016/j.mam.2008.05.005. PMC 2704241. PMID 18601945.
  18. ^ Franklin CC, et al. (2009). "Structure, function, and post-translational regulation of the catalytic and modifier subunits of glutamate cysteine ligase". Mol Aspects Med. 30 (1–2): 86–98. doi:10.1016/j.mam.2008.08.009. PMC 2714364. PMID 18812186.
  19. ^ Backos DS, et al. (2013). "Glycation of glutamate cysteine ligase by 2-deoxy-d-ribose and its potential impact on chemoresistance in glioblastoma". Neurochem Res. 38 (9): 1838–49. doi:10.1007/s11064-013-1090-4. PMID 23743623. S2CID 7738579.
  20. ^ McConnachie LA, Mohar I, et al. (2007). "Glutamate cysteine ligase modifier subunit deficiency and gender as determinants of acetaminophen-induced hepatotoxicity in mice". Toxicological Sciences. 99 (2): 628–636. doi:10.1093/toxsci/kfm165. PMID 17584759.
  21. ^ Backos DS, et al. (2013). "Glycation of glutamate cysteine ligase by 2-deoxy-d-ribose and its potential impact on chemoresistance in glioblastoma". Neurochem Res. 38 (9): 1838–49. doi:10.1007/s11064-013-1090-4. PMID 23743623. S2CID 7738579.
  22. ^ Dalton TP, Dieter MZ, Yang Y, Shertzer HG, Nebert DW (December 2000). "Knockout of the mouse glutamate cysteine ligase catalytic subunit (Gclc) gene: embryonic lethal when homozygous, and proposed model for moderate glutathione deficiency when heterozygous". Biochemical and Biophysical Research Communications. 279 (2): 324–9. doi:10.1006/bbrc.2000.3930. PMID 11118286.
  23. ^ Yang Y, Dieter MZ, Chen Y, Shertzer HG, Nebert DW, Dalton TP (December 2002). "Initial characterization of the glutamate-cysteine ligase modifier subunit Gclm(-/-) knockout mouse. Novel model system for a severely compromised oxidative stress response". The Journal of Biological Chemistry. 277 (51): 49446–52. doi:10.1074/jbc.M209372200. PMID 12384496.
  24. ^ Giordano G, Afsharinejad Z, Guizzetti M, Vitalone A, Kavanagh TJ, Costa LG (March 2007). "Organophosphorus insecticides chlorpyrifos and diazinon and oxidative stress in neuronal cells in a genetic model of glutathione deficiency". Toxicology and Applied Pharmacology. 219 (2–3): 181–9. doi:10.1016/j.taap.2006.09.016. PMID 17084875.
  25. ^ McConnachie LA, Mohar I, Hudson FN, Ware CB, Ladiges WC, Fernandez C, Chatterton-Kirchmeier S, White CC, Pierce RH, Kavanagh TJ (October 2007). "Glutamate cysteine ligase modifier subunit deficiency and gender as determinants of acetaminophen-induced hepatotoxicity in mice". Toxicological Sciences. 99 (2): 628–36. doi:10.1093/toxsci/kfm165. PMID 17584759.
  26. ^ Hothorn M, Wachter A, Gromes R, Stuwe T, Rausch T, Scheffzek K (September 2006). "Structural basis for the redox control of plant glutamate cysteine ligase". The Journal of Biological Chemistry. 281 (37): 27557–65. doi:10.1074/jbc.M602770200. PMID 16766527.
  27. ^ Hicks LM, Cahoon RE, Bonner ER, Rivard RS, Sheffield J, Jez JM (August 2007). "Thiol-based regulation of redox-active glutamate-cysteine ligase from Arabidopsis thaliana". The Plant Cell. 19 (8): 2653–61. doi:10.1105/tpc.107.052597. PMC 2002632. PMID 17766407.
  28. ^ Wachter A, Wolf S, Steininger H, Bogs J, Rausch T (January 2005). "Differential targeting of GSH1 and GSH2 is achieved by multiple transcription initiation: implications for the compartmentation of glutathione biosynthesis in the Brassicaceae". The Plant Journal. 41 (1): 15–30. doi:10.1111/j.1365-313X.2004.02269.x. PMID 15610346.
  29. ^ Lim B, Pasternak M, Meyer AJ, Cobbett CS (March 2013). "Restricting glutamylcysteine synthetase activity to the cytosol or glutathione biosynthesis to the plastid is sufficient for normal plant development and stress tolerance". Plant Biology. 16 (1): 58–67. doi:10.1111/plb.12033. PMID 23691990.
  30. ^ Pasternak M, Lim B, Wirtz M, Hell R, Cobbett CS, Meyer AJ (March 2008). "Restricting glutathione biosynthesis to the cytosol is sufficient for normal plant development". The Plant Journal. 53 (6): 999–1012. doi:10.1111/j.1365-313X.2007.03389.x. PMID 18088327.
  • MacKinnon, Charlotte M.; Carter, Philip E.; Smyth, S. Jane; Dunbar, Bryan; Fothergill, John E. (1987). "Molecular cloning of cDNA for human complement component C1s. The complete amino acid sequence". European Journal of Biochemistry. 169 (3): 547–553. doi:10.1111/j.1432-1033.1987.tb13644.x. PMID 3500856.
  • Snoke, JE; Yanari, S; Bloch, K (1953). "Synthesis of glutathione from gamma-glutamylcysteine". The Journal of Biological Chemistry. 201 (2): 573–586. doi:10.1016/S0021-9258(18)66212-X. PMID 13061393.
  • Mandeles, S; Block, K (1955). "Enzymatic synthesis of gamma-glutamylcysteine". The Journal of Biological Chemistry. 214 (2): 639–646. doi:10.1016/S0021-9258(18)70912-5. PMID 14381401.

April 10, 2024
glutamate, cysteine, ligase, previously, known, glutamylcysteine, synthetase, first, enzyme, cellular, glutathione, biosynthetic, pathway, that, catalyzes, chemical, reaction, identifiersec, 2cas, 9023, 7databasesintenzintenz, viewbrendabrenda, entryexpasynice. Glutamate cysteine ligase GCL EC 6 3 2 2 previously known as g glutamylcysteine synthetase GCS is the first enzyme of the cellular glutathione GSH biosynthetic pathway that catalyzes the chemical reaction Glutamate cysteine ligaseIdentifiersEC no 6 3 2 2CAS no 9023 64 7DatabasesIntEnzIntEnz viewBRENDABRENDA entryExPASyNiceZyme viewKEGGKEGG entryMetaCycmetabolic pathwayPRIAMprofilePDB structuresRCSB PDB PDBe PDBsumGene OntologyAmiGO QuickGOSearchPMCarticlesPubMedarticlesNCBIproteinsL glutamate L cysteine ATP displaystyle rightleftharpoons g glutamyl cysteine ADP PiGSH and by extension GCL is critical to cell survival Nearly every eukaryotic cell from plants to yeast to humans expresses a form of the GCL protein for the purpose of synthesizing GSH To further highlight the critical nature of this enzyme genetic knockdown of GCL results in embryonic lethality 1 Furthermore dysregulation of GCL enzymatic function and activity is known to be involved in the vast majority of human diseases such as diabetes Parkinson s disease Alzheimer s disease COPD HIV AIDS and cancer 2 3 This typically involves impaired function leading to decreased GSH biosynthesis reduced cellular antioxidant capacity and the induction of oxidative stress However in cancer GCL expression and activity is enhanced which serves to both support the high level of cell proliferation and confer resistance to many chemotherapeutic agents 4 Contents 1 Function 2 Regulation 3 Structure 3 1 Animal glutamate cysteine ligase 3 2 Plant glutamate cysteine ligase 4 ReferencesFunction editGlutamate cysteine ligase GCL catalyzes the first and rate limiting step in the production of the cellular antioxidant glutathione GSH involving the ATP dependent condensation of cysteine and glutamate to form the dipeptide gamma glutamylcysteine g GC 5 This peptide coupling is unique in that it occurs between the amino moiety of the cysteine and the terminal carboxylic acid of the glutamate side chain hence the name gamma glutamyl cysteine 6 This peptide bond is resistant to cleavage by cellular peptidases and requires a specialized enzyme gamma glutamyl transpeptidase gGT to metabolize g GC and GSH into its constituent amino acids 7 GCL enzymatic activity generally dictates cellular GSH levels and GSH biosynthetic capacity GCL enzymatic activity is influenced by numerous factors including cellular expression of the GCL subunit proteins access to substrates cysteine is typically limiting in the production of g GC the degree of negative feedback inhibition by GSH and functionally relevant post translational modifications to specific sites on the GCL subunits 8 9 10 Given its status as the rate limiting enzyme in GSH biosynthesis changes in GCL activity directly equate to changes in cellular GSH biosynthetic capacity 11 Therefore therapeutic strategies to alter GSH production have focused on this enzyme 12 Regulation editIn keeping with its critical importance in maintaining life GCL is subject to a multi level regulation of its expression function and activity GCL expression is regulated at the transcriptional transcription of the GCLC and GCLM DNA to make mRNA posttranscriptional the stability of the mRNA over time translational processing of the mRNA into protein and posttranslational levels involving modifications to the existing proteins 13 14 15 16 Although baseline constitutive expression is required to maintain cell viability expression of the GCL subunits is also inducible in response to oxidative stress GSH depletion and exposure to toxic chemicals with the Nrf2 AP 1 and NF kB transcription factors regulating the inducible and constitutive expression of both subunits 17 18 In terms of enzyme functional regulation GSH itself acts as a feedback inhibitor of GCL activity Under normal physiologic substrate concentrations the GCLC monomer alone may synthesize gamma glutamylcysteine however the normal physiologic levels of GSH estimated at around 5 mM far exceeds the GSH Ki for GCLC 19 suggesting that only the GCL holoenzyme is functional under baseline conditions However during oxidative stress or toxic insults that can result in the depletion of cellular GSH or its oxidation to glutathione disulfide GSSG the function of any monomeric GCLC in the cell is likely to become quite important In support of this hypothesis mice lacking expression of the GCLM subunit due to genetic knockdown exhibit low levels of tissue GSH 10 20 of the normal level which is roughly the level of the GSH Ki for monomeric GCLC 20 21 Structure editAnimal glutamate cysteine ligase edit Animal glutamate cysteine ligase GCL is a heterodimeric enzyme composed of two protein subunits that are coded by independent genes located on separate chromosomes Glutamate cysteine ligase catalytic subunit GCLC 73 kDa possesses all of substrate and cofactor binding sites and is responsible for all of the catalysis Glutamate cysteine ligase modifier subunit GCLM 31 kDa has no enzymatic activity on its own but increases the catalytic efficiency of GCLC when complexed in the holoenzyme In the majority of cells and tissues the expression of GCLM protein is lower than GCLC and GCLM is therefore limiting in the formation of the holoenzyme complex Thus the sum total of cellular GCL activity is equal to the activity of the holoenzyme the activity of the remaining monomeric GCLC composed of a catalytic and a modulatory subunit The catalytic subunit is necessary and sufficient for all GCL enzymatic activity whereas the modulatory subunit increases the catalytic efficiency of the enzyme Mice lacking the catalytic subunit i e lacking all de novo GSH synthesis die before birth 22 Mice lacking the modulatory subunit demonstrate no obvious phenotype but exhibit marked decrease in GSH and increased sensitivity to toxic insults 23 24 25 Plant glutamate cysteine ligase edit The plant glutamate cysteine ligase is a redox sensitive homodimeric enzyme conserved in the plant kingdom 26 In an oxidizing environment intermolecular disulfide bridges are formed and the enzyme switches to the dimeric active state The midpoint potential of the critical cysteine pair is 318 mV In addition to the redox dependent control the plant GCL enzyme is feedback inhibited by glutathione 27 GCL is exclusively located in plastids and glutathione synthetase GS is dual targeted to plastids and cytosol thus GSH and gamma glutamylcysteine are exported from the plastids 28 Studies also shown that restricting GCL activity to the cytosol or glutathione biosynthesis to the plastids is sufficient for normal plant development and stress tolerance 29 Both glutathione biosynthesis enzymes are essential in plants knock outs of GCL and GS are lethal to embryo and seedling respectively 30 As of late 2007 six structures have been solved for this class of enzymes with PDB accession codes 1V4G 1VA6 2D32 2D33 2GWC and 2GWD References edit Dalton TP et al 2004 Genetically altered mice to evaluate glutathione homeostasis in health and disease Free Radic Biol Med 37 10 1511 26 doi 10 1016 j freeradbiomed 2004 06 040 PMID 15477003 Lu SC 2009 Regulation of glutathione synthesis Mol Aspects Med 30 1 2 42 59 doi 10 1016 j mam 2008 05 005 PMC 2704241 PMID 18601945 Franklin CC et al 2009 Structure function and post translational regulation of the catalytic and modifier subunits of glutamate cysteine ligase Mol Aspects Med 30 1 2 86 98 doi 10 1016 j mam 2008 08 009 PMC 2714364 PMID 18812186 Backos DS et al 2012 The role of glutathione in brain tumor drug resistance Biochem Pharmacol 83 8 1005 12 doi 10 1016 j bcp 2011 11 016 PMID 22138445 Franklin CC et al 2009 Structure function and post translational regulation of the catalytic and modifier subunits of glutamate cysteine ligase Mol Aspects Med 30 1 2 86 98 doi 10 1016 j mam 2008 08 009 PMC 2714364 PMID 18812186 Njalsson R Norgren S 2005 Physiological and pathological aspects of GSH metabolism Acta Paediatr 94 2 132 137 doi 10 1080 08035250410025285 PMID 15981742 Lu SC 2009 Regulation of glutathione synthesis Mol Aspects Med 30 1 2 42 59 doi 10 1016 j mam 2008 05 005 PMC 2704241 PMID 18601945 Backos DS et al 2010 Manipulation of cellular GSH biosynthetic capacity via TAT mediated protein transduction of wild type or a dominant negative mutant of glutamate cysteine ligase alters cell sensitivity to oxidant induced cytotoxicity Toxicol Appl Pharmacol 243 1 35 45 doi 10 1016 j taap 2009 11 010 PMC 2819613 PMID 19914271 Backos DS et al 2011 Posttranslational modification and regulation of glutamate cysteine ligase by the a b unsaturated aldehyde 4 hydroxy 2 nonenal Free Radic Biol Med 50 1 14 26 doi 10 1016 j freeradbiomed 2010 10 694 PMC 3014730 PMID 20970495 Backos DS et al 2013 Glycation of glutamate cysteine ligase by 2 deoxy d ribose and its potential impact on chemoresistance in glioblastoma Neurochem Res 38 9 1838 49 doi 10 1007 s11064 013 1090 4 PMID 23743623 S2CID 7738579 Franklin CC et al 2009 Structure function and post translational regulation of the catalytic and modifier subunits of glutamate cysteine ligase Mol Aspects Med 30 1 2 86 98 doi 10 1016 j mam 2008 08 009 PMC 2714364 PMID 18812186 Griffith OW Meister A 1979 Potent and specific inhibition of glutathione synthesis by buthionine sulfoximine S n butyl homocysteine sulfoximine J Biol Chem 254 16 7558 60 doi 10 1016 S0021 9258 18 35980 5 PMID 38242 Lu SC 2009 Regulation of glutathione synthesis Mol Aspects Med 30 1 2 42 59 doi 10 1016 j mam 2008 05 005 PMC 2704241 PMID 18601945 Franklin CC et al 2009 Structure function and post translational regulation of the catalytic and modifier subunits of glutamate cysteine ligase Mol Aspects Med 30 1 2 86 98 doi 10 1016 j mam 2008 08 009 PMC 2714364 PMID 18812186 Backos DS et al 2011 Posttranslational modification and regulation of glutamate cysteine ligase by the a b unsaturated aldehyde 4 hydroxy 2 nonenal Free Radic Biol Med 50 1 14 26 doi 10 1016 j freeradbiomed 2010 10 694 PMC 3014730 PMID 20970495 Backos DS et al 2013 Glycation of glutamate cysteine ligase by 2 deoxy d ribose and its potential impact on chemoresistance in glioblastoma Neurochem Res 38 9 1838 49 doi 10 1007 s11064 013 1090 4 PMID 23743623 S2CID 7738579 Lu SC 2009 Regulation of glutathione synthesis Mol Aspects Med 30 1 2 42 59 doi 10 1016 j mam 2008 05 005 PMC 2704241 PMID 18601945 Franklin CC et al 2009 Structure function and post translational regulation of the catalytic and modifier subunits of glutamate cysteine ligase Mol Aspects Med 30 1 2 86 98 doi 10 1016 j mam 2008 08 009 PMC 2714364 PMID 18812186 Backos DS et al 2013 Glycation of glutamate cysteine ligase by 2 deoxy d ribose and its potential impact on chemoresistance in glioblastoma Neurochem Res 38 9 1838 49 doi 10 1007 s11064 013 1090 4 PMID 23743623 S2CID 7738579 McConnachie LA Mohar I et al 2007 Glutamate cysteine ligase modifier subunit deficiency and gender as determinants of acetaminophen induced hepatotoxicity in mice Toxicological Sciences 99 2 628 636 doi 10 1093 toxsci kfm165 PMID 17584759 Backos DS et al 2013 Glycation of glutamate cysteine ligase by 2 deoxy d ribose and its potential impact on chemoresistance in glioblastoma Neurochem Res 38 9 1838 49 doi 10 1007 s11064 013 1090 4 PMID 23743623 S2CID 7738579 Dalton TP Dieter MZ Yang Y Shertzer HG Nebert DW December 2000 Knockout of the mouse glutamate cysteine ligase catalytic subunit Gclc gene embryonic lethal when homozygous and proposed model for moderate glutathione deficiency when heterozygous Biochemical and Biophysical Research Communications 279 2 324 9 doi 10 1006 bbrc 2000 3930 PMID 11118286 Yang Y Dieter MZ Chen Y Shertzer HG Nebert DW Dalton TP December 2002 Initial characterization of the glutamate cysteine ligase modifier subunit Gclm knockout mouse Novel model system for a severely compromised oxidative stress response The Journal of Biological Chemistry 277 51 49446 52 doi 10 1074 jbc M209372200 PMID 12384496 Giordano G Afsharinejad Z Guizzetti M Vitalone A Kavanagh TJ Costa LG March 2007 Organophosphorus insecticides chlorpyrifos and diazinon and oxidative stress in neuronal cells in a genetic model of glutathione deficiency Toxicology and Applied Pharmacology 219 2 3 181 9 doi 10 1016 j taap 2006 09 016 PMID 17084875 McConnachie LA Mohar I Hudson FN Ware CB Ladiges WC Fernandez C Chatterton Kirchmeier S White CC Pierce RH Kavanagh TJ October 2007 Glutamate cysteine ligase modifier subunit deficiency and gender as determinants of acetaminophen induced hepatotoxicity in mice Toxicological Sciences 99 2 628 36 doi 10 1093 toxsci kfm165 PMID 17584759 Hothorn M Wachter A Gromes R Stuwe T Rausch T Scheffzek K September 2006 Structural basis for the redox control of plant glutamate cysteine ligase The Journal of Biological Chemistry 281 37 27557 65 doi 10 1074 jbc M602770200 PMID 16766527 Hicks LM Cahoon RE Bonner ER Rivard RS Sheffield J Jez JM August 2007 Thiol based regulation of redox active glutamate cysteine ligase from Arabidopsis thaliana The Plant Cell 19 8 2653 61 doi 10 1105 tpc 107 052597 PMC 2002632 PMID 17766407 Wachter A Wolf S Steininger H Bogs J Rausch T January 2005 Differential targeting of GSH1 and GSH2 is achieved by multiple transcription initiation implications for the compartmentation of glutathione biosynthesis in the Brassicaceae The Plant Journal 41 1 15 30 doi 10 1111 j 1365 313X 2004 02269 x PMID 15610346 Lim B Pasternak M Meyer AJ Cobbett CS March 2013 Restricting glutamylcysteine synthetase activity to the cytosol or glutathione biosynthesis to the plastid is sufficient for normal plant development and stress tolerance Plant Biology 16 1 58 67 doi 10 1111 plb 12033 PMID 23691990 Pasternak M Lim B Wirtz M Hell R Cobbett CS Meyer AJ March 2008 Restricting glutathione biosynthesis to the cytosol is sufficient for normal plant development The Plant Journal 53 6 999 1012 doi 10 1111 j 1365 313X 2007 03389 x PMID 18088327 MacKinnon Charlotte M Carter Philip E Smyth S Jane Dunbar Bryan Fothergill John E 1987 Molecular cloning of cDNA for human complement component C1s The complete amino acid sequence European Journal of Biochemistry 169 3 547 553 doi 10 1111 j 1432 1033 1987 tb13644 x PMID 3500856 Snoke JE Yanari S Bloch K 1953 Synthesis of glutathione from gamma glutamylcysteine The Journal of Biological Chemistry 201 2 573 586 doi 10 1016 S0021 9258 18 66212 X PMID 13061393 Mandeles S Block K 1955 Enzymatic synthesis of gamma glutamylcysteine The Journal of Biological Chemistry 214 2 639 646 doi 10 1016 S0021 9258 18 70912 5 PMID 14381401 Portal nbsp Biology Retrieved from https en wikipedia org w index php title Glutamate cysteine ligase amp oldid 1172348418, wikipedia, wiki, book, books, library,

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