Sydney Brenner Institute for Molecular Bioscience, Faculty of Health Sciences, University of the Witwatersrand, 9 Jubilee Road, Parktown, Johannesburg, 2193, South Africa.
Division of Human Genetics, National Health Laboratory Service and School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, 2001, South Africa.
Pharmacogenomics. 2023 Jul;24(10):561-578. doi: 10.2217/pgs-2023-0068. Epub 2023 Jul 28.
Cytochrome P450 (CYP) genetic variation largely impacts drug response. However, many CYP star alleles (haplotypes) lack functional annotation, impeding our understanding of drug metabolism mechanisms. We aimed to investigate the impact of missense variant combinations on CYP protein structures. Normal mode analysis was conducted on 261 missense variants within 91 CYP haplotypes. and were prioritized for molecular dynamics simulation. Normal mode analysis and molecular dynamics highlight the effects of known CYP missense variants on protein stability and conformational dynamics. Missense variants within haplotypes may have intermodulating effects on protein structure and function. This study highlights the utility of multiscale modeling in interpreting CYP missense variants and particularly their combinations within various star alleles.
细胞色素 P450(CYP)遗传变异在很大程度上影响药物反应。然而,许多 CYP 星等位基因(单倍型)缺乏功能注释,阻碍了我们对药物代谢机制的理解。我们旨在研究错义变异组合对 CYP 蛋白结构的影响。对 91 个 CYP 单倍型中的 261 个错义变异进行了正常模式分析,并对和进行了分子动力学模拟的优先级排序。正常模式分析和分子动力学突出了已知 CYP 错义变异对蛋白质稳定性和构象动力学的影响。单倍型内的错义变异可能对蛋白质结构和功能具有相互调节作用。本研究强调了多尺度建模在解释 CYP 错义变异及其在各种星等位基因中的组合方面的效用。