首页> 美国卫生研究院文献>Frontiers in Chemistry >Common G-Quadruplex Binding Agents Found to Interact With i-Motif-Forming DNA: Unexpected Multi-Target-Directed Compounds
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Common G-Quadruplex Binding Agents Found to Interact With i-Motif-Forming DNA: Unexpected Multi-Target-Directed Compounds

机译:发现与形成i-基序的DNA相互作用的常见G四联体结合剂:意外的多目标定向化合物。

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摘要

G-quadruplex (G4) and i-motif (iM) are four-stranded non-canonical nucleic acid structural arrangements. Recent evidences suggest that these DNA structures exist in living cells and could be involved in several cancer-related processes, thus representing an attractive target for anticancer drug discovery. Efforts toward the development of G4 targeting compounds have led to a number of effective bioactive ligands. Herein, employing several biophysical methodologies, we studied the ability of some well-known G4 ligands to interact with iM-forming DNA. The data showed that the investigated compounds are actually able to interact with both DNA in vitro, thus acting de facto as multi-target-directed agents. Interestingly, while all the compounds stabilize the G4, some of them significantly reduce the stability of the iM. The present study highlights the importance, when studying G4-targeting compounds, of evaluating also their behavior toward the i-motif counterpart.
机译:G-四链体(G4)和i-基序(iM)是四链的非规范核酸结构安排。最近的证据表明,这些DNA结构存在于活细胞中,并且可能参与了几种与癌症相关的过程,因此代表了抗癌药物发现的诱人靶标。致力于开发G4靶向化合物的努力已经导致了许多有效的生物活性配体。在这里,我们采用几种生物物理方法,研究了一些著名的G4配体与形成iM的DNA相互作用的能力。数据表明,所研究的化合物实际上能够在体外与两种DNA相互作用,因此实际上充当了多靶标定向剂。有趣的是,尽管所有化合物都能稳定G4,但其中一些化合物会显着降低iM的稳定性。本研究强调了在研究靶向G4的化合物时,还必须评估其对i-基序对应物的行为的重要性。

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