Non-covalent Metallo-Drugs: Using Shape to Target DNA and RNA Junctions and Other Nucleic Acid Structures.

Lucia Cardo, Michael J Hannon
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引用次数: 5

Abstract

The most effective class of anticancer drugs in clinical use are the platins which act by binding to duplex B-DNA. Yet duplex DNA is not DNA in its active form, and many other structures are formed in cells; for example, Y-shaped fork structures are involved in DNA replication and transcription and 4-way junctions with DNA repair. In this chapter we explore how large, cationic metallo-supramolecular structures can be used to bind to these less common, yet active, nucleic acid structures.

非共价金属药物:利用形状靶向DNA和RNA连接及其他核酸结构。
临床使用的最有效的一类抗癌药物是通过与双链B-DNA结合而起作用的铂。然而,双链DNA并不是活性形式的DNA,细胞中形成了许多其他结构;例如,y形叉结构参与DNA复制和转录,以及DNA修复的四向连接。在本章中,我们将探讨如何使用大型的阳离子金属超分子结构来结合这些不太常见但具有活性的核酸结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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