School of Chemical Sciences, University of Auckland, Private Bag 92019, Auckland 1142, New Zealand.
Metallomics. 2020 Nov 1;12(11):1627-1636. doi: 10.1039/d0mt00196a. Epub 2020 Oct 16.
Proteomics has played an important role in elucidating the fundamental processes occuring in living cells. Translating these methods to metallodrug research ('metalloproteomics') has provided a means for molecular target identification of metal-based anticancer agents which should signifcantly advance the research field. In combination with biological assays, these techniques have enabled the mechanisms of action of metallodrugs to be linked to their interactions with molecular targets and aid understanding of their biological properties. Such investigations have profoundly increased our knowledge of the complex and dynamic nature of metallodrug-biomolecule interactions and have provided, at least for some compound types, a more detailed picture on their specific protein-binding patterns. This perspective highlights the progression of metallodrug proteomics research for the identification of non-DNA targets from standard analytical techniques to powerful metallodrug pull-down methods.
蛋白质组学在阐明活细胞中发生的基本过程方面发挥了重要作用。将这些方法转化为金属药物研究(“金属蛋白质组学”)为确定基于金属的抗癌剂的分子靶标提供了一种手段,这将极大地推动该研究领域的发展。这些技术与生物测定法结合使用,使金属药物的作用机制与其与分子靶标的相互作用相关联,并有助于了解其生物学特性。此类研究极大地增加了我们对金属药物-生物分子相互作用的复杂和动态性质的了解,并为某些化合物类型至少提供了更详细的关于其特定蛋白质结合模式的信息。本综述重点介绍了金属药物蛋白质组学研究的进展,从标准分析技术到强大的金属药物下拉方法,以鉴定非 DNA 靶标。