K. Rajakumari , K. Aravind , M. Balamugundhan , Manjunathan Jagadeesan , Ambiga Somasundaram , Parthiban Brindha Devi , Pasiyappazham Ramasamy
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引用次数: 0
摘要
DNA 回旋酶是 DNA 拓扑异构酶蛋白家族的成员,能催化 DNA 的不同拓扑形式相互转化。它是导致 DNA 负向超螺旋的唯一酶。该酶由两个 GyrA("A")亚基和两个 GyrB("B")亚基组成四聚体。DNA 回旋酶是理想的药物治疗目标,因为它在细菌细胞中具有基本特性,而在真核生物中则缺乏回旋酶活性。抗菌药物,包括喹诺酮类药物和基于香豆素的衍生物,都是专门针对 DNA 回旋酶的。除了典型的抗生素结合位点(包括新生物素和氟喹诺酮类药物)外,其他几个领域也被用于药物研发。新型细菌 II 型拓扑异构酶抑制剂(NBTIs)包括西莫环酮(Simocyclinone)、噻吩(thiophene)、吉泊他星(gepotidacin)、位于苯基右侧(RHS)分子对位的卤素原子以及耦合细胞分裂 B(CcdB)。这些结合位点具有结构和化学活性,可抑制拓扑异构酶的超卷曲活性。本文概述了利用合成和天然前体抑制 DNA 回旋酶的情况,旨在进行药物开发和发现。
Comprehensive review of DNA gyrase as enzymatic target for drug discovery and development
DNA gyrase is a member of the DNA topoisomerase protein family that catalyzes the conversion of different topological forms of DNA into one another. It is the sole enzyme that causes DNA to negatively supercoil. The enzyme is tetrameric with two GyrA (“A") and two GyrB (“B") subunits. DNA gyrase is an ideal target for medication because of its basic properties in bacterial cells and the lack of gyrase activity in eukaryotes. Antibacterial medications, including quinolones and derivatives based on coumarins that specifically target DNA gyrase, underscore the significance of the enzyme in the fight against bacterial infections. In addition to the typical antibiotic-binding sites, including novobiocin and fluoroquinolones, several other areas are being used in drug discovery. Simocyclinone, thiophene, gepotidacin, halogen atoms in the para position of the phenyl right-hand side (RHS) moiety, and coupled cell division B (CcdB) are examples of novel bacterial type II topoisomerase inhibitors (NBTIs). These binding sites are structurally and chemically active and inhibit the supercoiling activity of topoisomerase. This article provides an overview of DNA gyrase inhibition using synthetic and natural precursors aimed at medication development and discovery.