| Literature DB >> 30311333 |
Chuanqi Zhao1, Hualong Song2, Peter Scott2, Andong Zhao3, Hisae Tateishi-Karimata4, Naoki Sugimoto4, Jinsong Ren1, Xiaogang Qu1.
Abstract
Natural d-DNA and l-DNA are mirror-image counterparts. However, because of the inherent flexibility and conformation diversity of DNA, it is still not clear how enantiomeric compounds recognize d-DNA and l-DNA. Herein, taking G-quadruplex (G4) DNA as an example that has diverse conformations and distinct biofunctions, the binding of ten pairs of iron triplex metallohelices to d- and l-G4 DNA were evaluated. The Δ-enantiomer binds to d-DNA and the Λ-enantiomer binds to l-DNA, exhibiting almost the same stabilization effect and binding affinity. The binding affinity of the Δ-metallohelix with d-G4 is nearly 70-fold higher than that of Λ-metallohelix binding d-G4. Δ-Metallohelix binding to d-G4 follows a two-step binding process driven by a favorable enthalpy contribution to compensate for the associated unfavorable entropy.Entities:
Keywords: DNA; chirality; helical structures; iron; supramolecular chemistry
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Year: 2018 PMID: 30311333 DOI: 10.1002/anie.201809207
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336