寡核苷酸
点击化学
DNA
铂金
组合化学
化学
计算生物学
分子生物学
生物化学
生物
催化作用
作者
Joseph Hennessy,Bríonna McGorman,Zara Molphy,Nicholas P. Farrell,Daniel Singleton,Tom Brown,Andrew Kellett
出处
期刊:Angewandte Chemie
[Wiley]
日期:2021-10-15
卷期号:61 (3): e202110455-e202110455
被引量:36
标识
DOI:10.1002/anie.202110455
摘要
Abstract Limitations of clinical platinum(II) therapeutics include systemic toxicity and inherent resistance. Modern approaches, therefore, seek new ways to deliver active platinum(II) to discrete nucleic acid targets. In the field of antigene therapy, triplex‐forming oligonucleotides (TFOs) have attracted interest for their ability to specifically recognise extended duplex DNA targets. Here, we report a click chemistry based approach that combines alkyne‐modified TFOs with azide‐bearing cis ‐platinum(II) complexes—based on cisplatin, oxaliplatin, and carboplatin motifs—to generate a library of Pt II ‐TFO hybrids. These constructs can be assembled modularly and enable directed platinum(II) crosslinking to purine nucleobases on the target sequence under the guidance of the TFO. By covalently incorporating modifications of thiazole orange—a known DNA‐intercalating fluorophore—into Pt II ‐TFOs constructs, enhanced target binding and discrimination between target and off‐target sequences was achieved.
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