Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, MC9743, 9500 Gilman Drive, La Jolla, CA 92093, USA.
Curr Opin Struct Biol. 2011 Apr;21(2):189-99. doi: 10.1016/j.sbi.2011.01.004. Epub 2011 Feb 1.
Here off-target binding implies the binding of a small molecule of therapeutic interest to a protein target other than the primary target for which it was intended. Increasingly such off-targeting appears to be the norm rather than the exception, rational drug design notwithstanding, and can lead to detrimental side-effects, or opportunities to reposition a therapeutic agent to treat a different condition. Not surprisingly, there is significant interest in determining a priori what off-targets exist on a proteome-wide scale. Beyond determining putative off-targets is the need to understand the impact of such binding on the complete biological system, with the ultimate goal of being able to predict the phenotypic outcome. While a very ambitious goal, some progress is being made.
这里的脱靶结合是指治疗性小分子与主要靶点以外的蛋白质靶标结合,而不是针对主要靶点。尽管进行了合理的药物设计,但这种脱靶结合的情况似乎越来越普遍,而不是例外,并且可能导致有害的副作用,或者有机会重新定位治疗剂来治疗不同的疾病。毫不奇怪,人们非常有兴趣在事先确定蛋白质组范围内存在哪些脱靶。除了确定可能的脱靶外,还需要了解这种结合对整个生物系统的影响,最终目标是能够预测表型结果。虽然这是一个非常有野心的目标,但已经取得了一些进展。