Quantitative Targeted Proteomics for Membrane Transporter Proteins: Method and Application

被引:0
|
作者
Xi Qiu
Hui Zhang
Yurong Lai
机构
[1] Pharmaceutical Candidate Optimization,
[2] Bristol-Myers Squibb,undefined
[3] Pharmacokinetics,undefined
[4] Dynamics,undefined
[5] and Metabolism,undefined
[6] Pfizer Global Research and Development,undefined
来源
The AAPS Journal | 2014年 / 16卷
关键词
drug absorption, distribution, metabolism, and excretion (ADME); drug transporters; extrapolations (IVIVE); LC-MS/MS; quantitative targeted proteomics;
D O I
暂无
中图分类号
学科分类号
摘要
Although global proteomics has shown promise for discovery of many new proteins, biomarkers, protein modifications, and polymorphisms, targeted proteomics is emerging in the proteomics research field as a complement to untargeted shotgun proteomics, particularly when a determined set of low-abundance functional proteins need to be measured. The function and expression of proteins related to drug absorption, distribution, metabolism, and excretion (ADME) such as cytochrome P450 enzymes and membrane transporters are of great interest in biopharmaceutical research. Since the variation in ADME-related protein expression is known to be a major complicating factor encountered during in vitro–in vivo and in vivo–in vivo extrapolations (IVIVE), the accurate quantification of the ADME proteins in complex biological systems becomes a fundamental element in establishing IVIVE for pharmacokinetic predictions. In this review, we provide an overview of relevant methodologies followed by a summary of recent applications encompassing mass spectrometry-based targeted quantifications of membrane transporters.
引用
收藏
页码:714 / 726
页数:12
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