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Genome-wide assessment of the carriers involved in the cellular uptake of drugs: a model system in yeast

机译:全基因组评估与细胞吸收药物有关的载体:酵母中的模型系统

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Background 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. Results 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. Conclusions 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.
机译:背景技术传统上认为药物吸收进入细胞主要是通过穿过细胞膜双层部分的被动扩散。最近对药物吸收主要是由载体介导的认识引起了以下问题:哪种药物使用哪种载体。结果为了解决这个问题,我们利用酵母发酵基因缺失集合构建了一个化学基因组学平台,利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。结论除了提供有用的平台技术外,这些结果进一步证实了以下观点:药物的细胞摄取通常是通过载体介导的运输发生的,并且表明建立此类载体的身份和组织分布应该是设计中的主要考虑因素。安全有效的药物。

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