Structure of Cytochrome P450 2C9*2 in Complex with Losartan: Insights into the Effect of Genetic Polymorphism.

dc.contributor.authorParikh, Sonia J
dc.contributor.authorEvans, Chiara M*
dc.contributor.authorObi, Juliet O*
dc.contributor.authorZhang, Qinghai
dc.contributor.authorMaekawa, Keiko
dc.contributor.authorGlass, Karen C
dc.contributor.authorShah, Manish B
dc.date.accessioned2023-11-22T14:43:17Z
dc.date.available2023-11-22T14:43:17Z
dc.date.issued2020-11
dc.description.abstractThe human CYP2C9 plays a crucial role in the metabolic clearance of a wide range of clinical therapeutics. The *2 allele is a prevalent genetic variation in CYP2C9 that is found in various populations. A marked reduction of catalytic activity toward many important drug substrates has been demonstrated by CYP2C9*2, which represents an amino acid variation at position 144 from arginine to cysteine. The crystal structure of CYP2C9*2 in complex with an antihypertensive drug losartan was solved using X-ray crystallography at 3.1-Å resolution. The Arg144Cys variation in the *2 complex disrupts the hydrogen-bonding interactions that were observed between the side chain of arginine and neighboring residues in the losartan complex of CYP2C9 and the wild-type (WT) ligand-free structure. The conformation of several secondary structural elements is affected, thereby altering the binding and orientation of drug and important amino acid side chains in the distal active site cavity. The new structure revealed distinct interactions of losartan in the compact active site of CYP2C9*2 and differed in occupancy at the other binding sites previously identified in the WT-losartan complex. Furthermore, the binding studies in solution using losartan illustrated lower activity of the CYP2C9*2 compared with the WT. Together, the findings yield valuable insights into the decreased hydroxylation activity of losartan in patients carrying CYP2C9*2 allele and provide a useful framework to investigate the effect of a single-nucleotide polymorphism that leads to altered metabolism of diverse drug substrates. SIGNIFICANCE STATEMENT: The *2 allele of the human drug-metabolizing enzyme CYP2C9 is found in different populations and results in significantly reduced activity toward various drug substrates. How the CYP2C9*2 variant induces altered drug metabolism is poorly understood given that the Arg144Cys variation is located far away from the active site. This work yield insight into the effect of distal variation using multitude of techniques that include X-ray crystallography, isothermal titration calorimetry, enzymatic characterization, and computational studies.
dc.description.grantGrant Funded
dc.description.sponsorshipP41 GM103393/GM/NIGMS NIH HHS/United States
dc.description.urihttps://doi.org/10.1124/molpharm.120.000042
dc.description.urihttp://www.ncbi.nlm.nih.gov/pmc/articles/pmc7569312
dc.identifier.citationParikh SJ, Evans CM, Obi JO, Zhang Q, Maekawa K, Glass KC, Shah MB. Structure of Cytochrome P450 2C9*2 in Complex with Losartan: Insights into the Effect of Genetic Polymorphism. Mol Pharmacol. 2020 Nov;98(5):529-539. doi: 10.1124/molpharm.120.000042. Epub 2020 Sep 16. PMID: 32938720; PMCID: PMC7569312.
dc.identifier.issn0026-895X
dc.identifier.other32938720
dc.identifier.urihttps://hdl.handle.net/20.500.14303/416
dc.language.isoen
dc.publisherAmerican Society for Pharmacology and Experimental Therapeutics
dc.relation.ispartofMolecular Pharmacology
dc.rightsThis Item is protected by copyright and/or related rights. You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s). http://rightsstatements.org/vocab/InC/1.0/
dc.subjectCytochrome P-450 CYP2C9 / genetics
dc.subjectLosartan / chemistry
dc.subjectPolymorphism, Single Nucleotide / genetics
dc.subjectAntihypertensive Agents / chemistry
dc.titleStructure of Cytochrome P450 2C9*2 in Complex with Losartan: Insights into the Effect of Genetic Polymorphism.
dc.typeArticle
local.departmentprogramDepartment of Pharmaceutical Sciences
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