Biomol Ther.  2019 Nov;27(6):577-583. 10.4062/biomolther.2019.112.

Functional Characterization of Pharmcogenetic Variants of Human Cytochrome P450 2C9 in Korean Populations

• Cho MA
• Yoon JG
• Kim V
• Kim H
• Lee R
• Lee MG
• Kim D

• KMID: 2462885
• DOI: http://doi.org/10.4062/biomolther.2019.112

Abstract

Human cytochrome P450 2C9 is a highly polymorphic enzyme that is required for drug and xenobiotic metabolism. Here, we studied eleven P450 2C9 genetic variants"”including three novel variants F69S, L310V, and Q324X"”that were clinically identified in Korean patients. P450 2C9 variant enzymes were expressed in Escherichia coli and their bicistronic membrane fractions were prepared The CO-binding spectra were obtained for nine enzyme variants, indicating P450 holoenzymes, but not for the M02 (L90P) variant. The M11 (Q324X) variant could not be expressed due to an early nonsense mutation. LC-MS/MS analysis was performed to measure the catalytic activities of the P450 2C9 variants, using diclofenac as a substrate. Steady-state kinetic analysis revealed that the catalytic efficiency of all nine P450 2C9 variants was lower than that of the wild type P450 2C9 enzyme. The M05 (R150L) and M06 (P279T) variants showed high k(cat) values; however, their K(m) values were also high. As the M01 (F69S), M03 (R124Q), M04 (R125H), M08 (I359L), M09 (I359T), and M10 (A477T) variants exhibited higher K(m) and lower k(cat) values than that of the wild type enzyme, their catalytic efficiency decreased by approximately 50-fold compared to the wild type enzyme. Furthermore, the novel variant M07 (L310V) showed lower k(cat) and K(m) values than the wild type enzyme, which resulted in its decreased (80%) catalytic efficiency. The X-ray crystal structure of P450 2C9 revealed the presence of mutations in the residues surrounding the substrate-binding cavity. Functional characterization of these genetic variants can help understand the pharmacogenetic outcomes.

Keyword

Cytochrome P450; P450 2C9; Diclofenac; Polymorphism; Pharmacogenetics

MeSH Terms

Codon, Nonsense
Cytochrome P-450 Enzyme System*
Cytochromes*
Diclofenac
Escherichia coli
Holoenzymes
Humans*
Membranes
Metabolism
Pharmacogenetics
Codon, Nonsense
Cytochrome P-450 Enzyme System
Cytochromes
Diclofenac
Holoenzymes