Aldehyde oxidase

Aldehyde oxidase (AO) is a metabolizing enzyme, located in the cytosolic compartment of tissues in many organisms. AO catalyzes the oxidation of aldehydes into carboxylic acid, and in addition, catalyzes the hydroxylation of some heterocycles.[1] It can also catalyze the oxidation of both cytochrome P450 (CYP450) and monoamine oxidase (MAO) intermediate products. AO plays an important role in the metabolism of several drugs.

Not to be confused with aldehyde dehydrogenase.
Aldehyde oxidase
Model of human aldehyde oxidase after PDB: 4UHW​.
Identifiers
EC number1.2.3.1
CAS number9029-07-6
Databases
IntEnzIntEnz view
BRENDABRENDA entry
ExPASyNiceZyme view
KEGGKEGG entry
MetaCycmetabolic pathway
PRIAMprofile
PDB structuresRCSB PDB PDBe PDBsum
Gene OntologyAmiGO / QuickGO
aldehyde oxidase 1
Identifiers
SymbolAOX1
NCBI gene316
HGNC553
OMIM602841
RefSeqNM_001159
UniProtQ06278
Other data
EC number1.2.3.1
LocusChr. 2 q33

Reaction

AO catalyzes the conversion of an aldehyde in the presence of oxygen and water to an acid and hydrogen peroxide.

  • an aldehyde + H2O + O2 ⇌ a carboxylate + H2O2 + H+

Though the enzyme uses molecular oxygen as an electron acceptor, the oxygen atom that is incorporated into the carboxylate product is from water; however, the exact mechanism of reduction is still not known for AO.

The AO also catalyzes the oxidation of heterocycles, which involves a nucleophilic attack located at the carbon atom beside the heteroatom. This means that susceptibility to nucleophilic attack of a heterocycle determines if that heterocycle is a suitable substrate for AO.

Species distribution

Aldehyde oxidase is a member of the molybd-flavo protein family[1] and has a very complex evolutionary profile—as the genes of AO varies according to animal species.[2] Higher primates, such as humans, have a single functioning AO gene (AOX1), whereas rodents have four separate AOX genes. The human population has both functionally inactive hAOX1 allelic variants and encoding enzyme variants with different catalytic activities. AO activity has been found to be much more active in higher primates (compared to rodents), though many factors may affect this activity, such as gender, age, cigarette smoking, drug usage, and disease states.

Tissue distribution

Aldehyde oxidase is very concentrated in the liver, where it oxidizes multiple aldehydes and nitrogenous heterocyclic compounds, such as anti-cancer and immunosuppressive drugs.[1] Some AO activity has been located in other parts of the body—including the lungs (epithelial cells and alveolar cells), the kidneys, and the gastrointestinal tract (small and large intestines).

Regulation

The regulation of expression of AO is still not completely known, though some studies have shown that the AOX1 gene is regulated by the Nrf2 pathway.[3] Some known inhibitors of AO are sterol and phenol compounds, like estradiol. Others include amsacrine, 6,6'-azopurine, chlorpromazine, cimetidine, cyanide, diethylstilbestrol, genestein, isovanillin, and methadone.

Structure

AO is very similar in amino acid sequence to xanthine oxidase (XO). The active sites of AO has been found to have a superimposed structure to that of XO, in studies involving mouse liver. AO is a homodimer, and requires FAD, molybdenum (MoCo) and two 2Fe-2S clusters as cofactors. These two 2Fe-2S cofactors each bind to the two distinct 150-kDa monomers of AO. Three separate domains harbor these three requirements. There is a 20 kDa N-terminal which binds to the two 2Fe-2S cofactors, a 40 kDa domain which provides a means of binding to the FAD, and a C-terminal which houses the molybdenum.[4]

Role in drug metabolism

Aldehyde oxidase is thought to have a significant impact on pharmacokinetics. AO is capable of oxidizing many drugs in the liver (such as N-1-methylnicotinamide, N-methylphthalazinium, benzaldehyde, retinal, and vanillin), because of its broad substrate specificity.[5] AO greatly contributes to the hepatic clearance of drugs and other compounds.[6] For example, cytoplasmic AOX1 a key enzyme in the hepatic phase I metabolism of several xenobiotics.[2] For this reason, AOX genes are becoming increasingly important to both understand and control in the therapeutic drug industry.[2] Pfizer TLR7 agonist program has found several techniques to switch the AO metabolism off.[7]

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gollark: Oh no. My Raspberry Pi and/or its power supply are undergoing apiosis.
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See also

References
  1. Gordon AH, Green DE, Subrahmanyan V (May 1940). "Liver aldehyde oxidase". The Biochemical Journal. 34 (5): 764–74. doi:10.1042/bj0340764. PMC 1265340. PMID 16747217.
  2. Garattini E, Terao M (Apr 2012). "The role of aldehyde oxidase in drug metabolism". Expert Opinion on Drug Metabolism & Toxicology. 8 (4): 487–503. doi:10.1517/17425255.2012.663352. PMID 22335465.
  3. Maeda K, Ohno T, Igarashi S, Yoshimura T, Yamashiro K, Sakai M (Sep 2012). "Aldehyde oxidase 1 gene is regulated by Nrf2 pathway". Gene. 505 (2): 374–8. doi:10.1016/j.gene.2012.06.010. hdl:2115/50082. PMID 22705828.
  4. Pryde DC, Dalvie D, Hu Q, Jones P, Obach RS, Tran TD (Dec 2010). "Aldehyde oxidase: an enzyme of emerging importance in drug discovery". Journal of Medicinal Chemistry. 53 (24): 8441–60. doi:10.1021/jm100888d. PMID 20853847.
  5. Strelevitz TJ, Orozco CC, Obach RS (Jul 2012). "Hydralazine as a selective probe inactivator of aldehyde oxidase in human hepatocytes: estimation of the contribution of aldehyde oxidase to metabolic clearance". Drug Metabolism and Disposition. 40 (7): 1441–8. doi:10.1124/dmd.112.045195. PMID 22522748.
  6. Hartmann T, Terao M, Garattini E, Teutloff C, Alfaro JF, Jones JP, Leimkühler S (May 2012). "The impact of single nucleotide polymorphisms on human aldehyde oxidase". Drug Metabolism and Disposition. 40 (5): 856–64. doi:10.1124/dmd.111.043828. PMC 4738704. PMID 22279051.
  7. Pryde DC, Tran TD, Jones P, Duckworth J, Howard M, Gardner I, Hyland R, Webster R, Wenham T, Bagal S, Omoto K, Schneider RP, Lin J (Apr 2012). "Medicinal chemistry approaches to avoid aldehyde oxidase metabolism". Bioorganic & Medicinal Chemistry Letters. 22 (8): 2856–60. doi:10.1016/j.bmcl.2012.02.069. PMID 22429467.
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