Biology:Dimethylargininase
| dimethylargininase | |||||||||
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 Ribbon diagram of human DDAH1.[1] | |||||||||
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| EC number | 3.5.3.18 | ||||||||
| CAS number | 123644-75-7 | ||||||||
| Databases | |||||||||
| IntEnz | IntEnz view | ||||||||
| BRENDA | BRENDA entry | ||||||||
| ExPASy | NiceZyme view | ||||||||
| KEGG | KEGG entry | ||||||||
| MetaCyc | metabolic pathway | ||||||||
| PRIAM | profile | ||||||||
| PDB structures | RCSB PDB PDBe PDBsum | ||||||||
| Gene Ontology | AmiGO / QuickGO | ||||||||
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In the field of enzymology, a dimethylargininase, also known as a dimethylarginine dimethylaminohydrolase (DDAH), is an enzyme that catalyzes the chemical reaction:
- N-omega,N-omega'-methyl-L-arginine + H2O [math]\displaystyle{ \rightleftharpoons }[/math] dimethylamine + L-citrulline
Thus, the two substrates of this enzyme are N-omega,N-omega'-methyl-L-arginine and H2O, whereas its two products are dimethylamine and L-citrulline.
Isozymes
Dimethylarginine dimethylaminohydrolase is an enzyme found in all mammalian cells. Two isoforms exist, DDAH I and DDAH II, with some differences in tissue distribution of the two isoforms[2]). The enzyme degrades methylarginines, specifically asymmetric dimethylarginine (ADMA) and NG-monomethyl-L-arginine (MMA).
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Function
The methylarginines ADMA and MMA inhibit the enzyme nitric oxide synthase.[3] As such, DDAH is important in removing methylarginines, generated by protein degradation, from accumulating and inhibiting the generation of nitric oxide.
Clinical significance
Inhibition of DDAH activity causes methylarginines to accumulate, blocking nitric oxide(NO) synthesis and causing vasoconstriction.[4] An impairment of DDAH activity appears to be involved in the elevation of plasma ADMA, and impairment of vascular relaxation observed in humans with cardiovascular disease or risk factors (such as hypercholesterolemia, diabetes mellitus, and insulin resistance). The activity of DDAH is impaired by oxidative stress, permitting ADMA to accumulate. A wide range of pathologic stimuli induce endothelial oxidative stress such as oxidized LDL-cholesterol, inflammatory cytokines, hyperhomocysteinemia, hyperglycemia and infectious agents. Each of these insults attenuates DDAH activity in vitro and in vivo.[5][6][7][8] The attenuation of DDAH allows ADMA to accumulate, and to block NO synthesis. The adverse effect of these stimuli can be reversed in vitro by antioxidants, which preserve the activity of DDAH.
The sensitivity of DDAH to oxidative stress is conferred by a critical sulfhydryl in the active site of the enzyme that is required for the metabolism of ADMA. This sulfhydryl can also be reversibly inhibited by NO in an elegant form of negative feedback.[9] Homocysteine (a putative cardiovascular risk factor) mounts an oxidative attack on DDAH to form a mixed disulfide, inactivating the enzyme.[6] By oxidizing a sulfhydryl moiety critical for DDAH activity, homocysteine and other risk factors cause ADMA to accumulate and to suppress nitric oxide synthase (NOS) activity.
The critical role of DDAH activity in regulating NO synthesis in vivo was demonstrated using a transgenic DDAH mouse.[10] In this animal, the activity of DDAH is increased, and plasma ADMA levels are reduced by 50%. The reduction in plasma ADMA is associated with a significant increase in NOS activity, as plasma and urinary nitrate levels are doubled. The increase in NOS activity translates into a 15mmHg reduction in systolic blood pressure in the transgenic mouse. This study provides evidence for the importance of DDAH activity and plasma ADMA levels in the regulation of NO synthesis. Subsequent studies have shown that DDAH transgenic animals also manifest improvements in endothelial regeneration and angiogenesis, and reduced vascular obstructive disease, in association with the reduced plasma levels of ADMA.[11][12] These findings are consistent with evidence from a number of groups that nitric oxide plays a critical role in vascular regeneration. By contrast, elevations in ADMA impair angiogenesis. These insights into the role of DDAH in degrading endogenous inhibitors of NOS, and thereby maintaining vascular NO production, may have important implications in vascular health and therapy for cardiovascular disease.
See also
- Protein detoxification
References
- ↑ PDB: 3I2E; "Developing Dual and Specific Inhibitors of Dimethylarginine Dimethylaminohydrolase-1 and Nitric Oxide Synthase: Toward a Targeted Polypharmacology To Control Nitric Oxide". Biochemistry 48 (36): 8624–8635. 2009. doi:10.1021/bi9007098. PMID 19663506.; rendered via PyMOL.
- ↑ Leiper JM, Santa Maria J, Chubb A et al. Identification of two human dimethylarginine dimethylaminohydrolases with distinct tissue distributions and homology with microbial arginine deiminases. Biochem J. 1999; 343: 209-214.
- ↑ Cooke JP (April 2004). "Asymmetrical dimethylarginine: the Uber marker?". Circulation 109 (15): 1813–1818. doi:10.1161/01.CIR.0000126823.07732.D5. PMID 15096461.
- ↑ "Regulation of nitric oxide synthesis by dimethylarginine dimethylaminohydrolase". Br. J. Pharmacol. 119 (8): 1533–40. December 1996. doi:10.1111/j.1476-5381.1996.tb16069.x. PMID 8982498.
- ↑ "Novel mechanism for endothelial dysfunction: dysregulation of dimethylarginine dimethylaminohydrolase". Circulation 99 (24): 3092–5. June 1999. doi:10.1161/01.cir.99.24.3092. PMID 10377069.
- ↑ 6.0 6.1 "Homocysteine impairs the nitric oxide synthase pathway: role of asymmetric dimethylarginine". Circulation 104 (21): 2569–2575. November 2001. doi:10.1161/hc4601.098514. PMID 11714652.
- ↑ "Impaired nitric oxide synthase pathway in diabetes mellitus: role of asymmetric dimethylarginine and dimethylarginine dimethylaminohydrolase". Circulation 106 (8): 987–992. August 2002. doi:10.1161/01.CIR.0000027109.14149.67. PMID 12186805.
- ↑ "Cytomegalovirus infection impairs the nitric oxide synthase pathway: role of asymmetric dimethylarginine in transplant arteriosclerosis". Circulation 109 (4): 500–505. February 2004. doi:10.1161/01.CIR.0000109692.16004.AF. PMID 14732750.
- ↑ "S-nitrosylation of dimethylarginine dimethylaminohydrolase regulates enzyme activity: further interactions between nitric oxide synthase and dimethylarginine dimethylaminohydrolase". Proc. Natl. Acad. Sci. U.S.A. 99 (21): 13527–13532. October 2002. doi:10.1073/pnas.212269799. PMID 12370443. Bibcode: 2002PNAS...9913527L.
- ↑ "Dimethylarginine dimethylaminohydrolase regulates nitric oxide synthesis: genetic and physiological evidence". Circulation 108 (24): 3042–3047. December 2003. doi:10.1161/01.CIR.0000101924.04515.2E. PMID 14638548.
- ↑ "Overexpression of dimethylarginine dimethylaminohydrolase reduces tissue asymmetric dimethylarginine levels and enhances angiogenesis". Circulation 111 (11): 1431–1438. March 2005. doi:10.1161/01.CIR.0000158487.80483.09. PMID 15781754.
- ↑ "Dimethylarginine dimethylaminohydrolase overexpression suppresses graft coronary artery disease". Circulation 112 (11): 1549–1556. September 2005. doi:10.1161/CIRCULATIONAHA.105.537670. PMID 16144995.
Further reading
- "Purification and properties of a new enzyme, NG,NG-dimethylarginine dimethylaminohydrolase, from rat kidney". J. Biol. Chem. 264 (17): 10205–9. 1989. doi:10.1016/S0021-9258(18)81786-0. PMID 2722865.
External links
- dimethylarginine+dimethylaminohydrolase at the US National Library of Medicine Medical Subject Headings (MeSH)
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