Genomics Institute of the Novartis Research Foundation, 10675 John Jay Hopkins Drive, San Diego, CA 92121, USA.
Future Microbiol. 2011 Jun;6(6):693-704. doi: 10.2217/fmb.11.45.
It has been recognized that new antimalarials with a novel mode of action are critical to combat the continued emergence and dissemination of drug-resistant parasites that threaten the efficacy of current malaria treatments. Thus, recent high-throughput screening campaigns have been initiated using asexual intraerythrocytic stage cell-based assays of Plasmodium falciparum. These have led to the unprecedented identification of over 10,000 new antimalarial compounds. Inherently, novel compounds identified by cell-based assays will have poorly defined modes of action. While some of these compounds may have recognizable targets, the majority of cell-based hits are comprised of unique chemical scaffolds usually lacking cross-resistance with known drugs. It is likely that these novel antimalarial scaffolds will reveal new targets. A challenge for the community will be to assign these small molecules to their targets. In this article, we review methodologies to assist in the determination of a compound's mode of action.
人们已经认识到,具有新作用模式的新型抗疟药物对于对抗不断出现和传播的耐药寄生虫至关重要,这些寄生虫威胁着当前疟疾治疗的疗效。因此,最近已经启动了使用基于疟原虫无性红内期细胞的高通量筛选活动。这导致了超过 10000 种新型抗疟化合物的空前鉴定。从本质上讲,基于细胞的测定方法所鉴定的新型化合物的作用模式将定义不佳。虽然其中一些化合物可能具有可识别的靶标,但大多数基于细胞的命中化合物由独特的化学结构组成,通常与已知药物没有交叉耐药性。这些新型抗疟药物结构很可能会揭示新的靶标。对于该领域来说,一个挑战将是将这些小分子分配到它们的靶标上。在本文中,我们综述了有助于确定化合物作用模式的方法学。