Department of Pharmaceutical Microbiology, Faculty of Life Sciences, Kumamoto University, 5-1 Oe-honmachi, Chuo-ku, Kumamoto 862-0973, Japan; Department of Pharmaceutical Microbiology, School of Pharmacy, Kumamoto University, 5-1 Oe-honmachi, Chuo-ku, Kumamoto 862-0973, Japan.
Department of Pharmaceutical Microbiology, School of Pharmacy, Kumamoto University, 5-1 Oe-honmachi, Chuo-ku, Kumamoto 862-0973, Japan.
Drug Metab Pharmacokinet. 2021 Feb;36:100361. doi: 10.1016/j.dmpk.2020.09.006. Epub 2020 Sep 30.
Proteomics refers to the large-scale study of proteins, providing comprehensive and quantitative information on proteins in tissue, blood, and cell samples. In many studies, proteomics utilizes liquid chromatography-mass spectrometry. Proteomics has developed from a qualitative methodology of protein identification to a quantitative methodology for comparing protein expression, and it is currently classified into two distinct methodologies: quantitative and targeted proteomics. Quantitative proteomics comprehensively identifies proteins in samples, providing quantitative information on large-scale comparative profiles of protein expression. Targeted proteomics simultaneously quantifies only target proteins with high sensitivity and specificity. Therefore, in biomarker research, quantitative proteomics is used for the identification of biomarker candidates, and targeted proteomics is used for the validation of biomarkers. Understanding the specific characteristics of each method is important for conducting appropriate proteomics studies. In this review, we introduced the different characteristics and applications of quantitative and targeted proteomics, and then discussed the results of our recent proteomics studies that focused on the identification and validation of biomarkers of drug efficacy. These findings may enable us to predict the outcomes of cancer therapy and drug-drug interactions with antibiotics through changes in the intestinal microbiome.
蛋白质组学是指对蛋白质进行大规模研究,提供组织、血液和细胞样本中蛋白质的全面和定量信息。在许多研究中,蛋白质组学利用液相色谱-质谱联用技术。蛋白质组学已经从蛋白质鉴定的定性方法发展为比较蛋白质表达的定量方法,目前分为两种截然不同的方法:定量蛋白质组学和靶向蛋白质组学。定量蛋白质组学全面鉴定样本中的蛋白质,提供大规模比较蛋白质表达的定量信息。靶向蛋白质组学则具有高灵敏度和特异性,同时定量仅针对目标蛋白质。因此,在生物标志物研究中,定量蛋白质组学用于鉴定生物标志物候选物,靶向蛋白质组学用于验证生物标志物。了解每种方法的具体特点对于进行适当的蛋白质组学研究非常重要。在这篇综述中,我们介绍了定量和靶向蛋白质组学的不同特点和应用,然后讨论了我们最近的蛋白质组学研究结果,这些研究集中于药物疗效生物标志物的鉴定和验证。这些发现可能使我们能够通过肠道微生物组的变化来预测癌症治疗和抗生素药物相互作用的结果。