7OTB

Ruthenium polypridyl complex bound to a unimolecular chair-form G-quadruplex

7OTB の概要

• エントリーDOI: 10.2210/pdb7otb/pdb
• 分子名称: DNA (5'-D(*GP*GP*GP*TP*TP*AP*GP*GP*GP*TP*TP*AP*GP*GP*GP*TP*TP*TP*GP*GP*G)-3'), POTASSIUM ION, BARIUM ION, ... (5 entities in total)
• 機能のキーワード: ruthenium, g-quadruplex, chair, telomeric, dna
• 由来する生物種: synthetic construct
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 7828.88

構造登録者

McQuaid, K.T.,Cardin, C.J.,Hall, J.P.,Paterson, N.G.,Baumgaertner, L. (登録日: 2021-06-09, 公開日: 2022-04-06, 最終更新日: 2024-06-19)

主引用文献

McQuaid, K.T.,Takahashi, S.,Baumgaertner, L.,Cardin, D.J.,Paterson, N.G.,Hall, J.P.,Sugimoto, N.,Cardin, C.J.
Ruthenium Polypyridyl Complex Bound to a Unimolecular Chair-Form G-Quadruplex.
J.Am.Chem.Soc., 144:5956-5964, 2022

PubMed Abstract: The DNA G-quadruplex is known for forming a range of topologies and for the observed lability of the assembly, consistent with its transient formation in live cells. The stabilization of a particular topology by a small molecule is of great importance for therapeutic applications. Here, we show that the ruthenium complex Λ-[Ru(phen)(qdppz)] displays enantiospecific G-quadruplex binding. It crystallized in 1:1 stoichiometry with a modified human telomeric G-quadruplex sequence, GGGTTAGGGTTAGGGTTTGGG (T), in an antiparallel chair topology, the first structurally characterized example of ligand binding to this topology. The lambda complex is bound in an intercalation cavity created by a terminal G-quartet and the central narrow lateral loop formed by T-T-A. The two remaining wide lateral loops are linked through a third K ion at the other end of the G-quartet stack, which also coordinates three thymine residues. In a comparative ligand-binding study, we showed, using a Klenow fragment assay, that this complex is the strongest observed inhibitor of replication, both using the native human telomeric sequence and the modified sequence used in this work.

PubMed: 35324198
DOI: 10.1021/jacs.2c00178

実験手法

X-RAY DIFFRACTION (1.6 Å)