Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543, Singapore.
Nat Prod Rep. 2016 May 4;33(5):612-20. doi: 10.1039/c5np00101c.
Covering: 2010 to 2014.Advances in isolation, synthesis and screening strategies have made many bioactive substances available. However, in most cases their putative biological targets remain unknown. Herein, we highlight recent advances in target identification of natural products and bioactive compounds by using affinity-based probes. Aided by photoaffinity labelling, this strategy can capture potential cellular targets (on and off) of a natural product or bioactive compound in live cells directly, even when the compound-target interaction is reversible with moderate affinity. The knowledge of these targets may help uncover molecular pathways and new therapeutics for currently untreatable diseases. In this highlight, we will introduce the development of various photoactivatable groups, their synthesis and applications in target identification of natural products and bioactive compounds, with a focus on work done in recent years and from our laboratory. We will further discuss the strengths and weaknesses of each group and the outlooks for this novel proteome-wide profiling strategy.
2010 年至 2014 年。通过分离、合成和筛选策略的进步,许多具有生物活性的物质已经可以获得。然而,在大多数情况下,它们假定的生物靶标仍然未知。在此,我们通过利用基于亲和性的探针强调了天然产物和生物活性化合物的靶标鉴定的最新进展。在光亲和标记的辅助下,该策略可以直接在活细胞中捕获天然产物或生物活性化合物的潜在细胞靶标(开和关),即使化合物-靶标相互作用具有中等亲和力的可逆性。这些靶标的知识可能有助于揭示目前无法治疗的疾病的分子途径和新的治疗方法。在这个亮点中,我们将介绍各种光活化基团的发展、它们的合成以及在天然产物和生物活性化合物靶标鉴定中的应用,重点介绍近年来我们实验室的工作。我们将进一步讨论每个基团的优缺点以及这种新型蛋白质组范围分析策略的前景。