School of Chemistry, University of Manchester, Manchester, UK.
BMC Biol. 2011 Oct 24;9:70. doi: 10.1186/1741-7007-9-70.
The uptake of drugs into cells has traditionally been considered to be predominantly via passive diffusion through the bilayer portion of the cell membrane. The recent recognition that drug uptake is mostly carrier-mediated raises the question of which drugs use which carriers.
To answer this, we have constructed a chemical genomics platform built upon the yeast gene deletion collection, using competition experiments in batch fermenters and robotic automation of cytotoxicity screens, including protection by 'natural' substrates. Using these, we tested 26 different drugs and identified the carriers required for 18 of the drugs to gain entry into yeast cells.
As well as providing a useful platform technology, these results further substantiate the notion that the cellular uptake of pharmaceutical drugs normally occurs via carrier-mediated transport and indicates that establishing the identity and tissue distribution of such carriers should be a major consideration in the design of safe and effective drugs.
传统上,细胞内药物摄取被认为主要是通过细胞膜双层部分的被动扩散。最近人们认识到,药物摄取主要是通过载体介导的,这就提出了一个问题,即哪些药物使用哪些载体。
为了回答这个问题,我们构建了一个基于酵母基因缺失文库的化学基因组学平台,使用分批发酵罐中的竞争实验和细胞毒性筛选的机器人自动化,包括“天然”底物的保护。使用这些,我们测试了 26 种不同的药物,并确定了 18 种药物进入酵母细胞所需的载体。
除了提供一个有用的平台技术外,这些结果进一步证实了这样一种观点,即药物的细胞摄取通常是通过载体介导的运输发生的,并表明确定此类载体的身份和组织分布应该是安全有效药物设计的一个主要考虑因素。