6GLD

Intercalation of [Ru(TAP)2(11-Br-dppz)]2+ bound to d(TCGGCGCCGA)2

6GLD の概要

• エントリーDOI: 10.2210/pdb6gld/pdb
• 分子名称: d(TCGGCGCCGA)2, BARIUM ION, Ruthenium (bis-(tetraazaphenanthrene)) (11-bromo-dipyridophenazine), ... (4 entities in total)
• 機能のキーワード: ruthenium, intercalation, dna, asymmetric
• 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: 4009.95

構造登録者

McQuaid, K.T.,Hall, J.P.,Cardin, C.J. (登録日: 2018-05-23, 公開日: 2019-06-19, 最終更新日: 2024-05-15)

主引用文献

McQuaid, K.,Hall, J.P.,Brazier, J.A.,Cardin, D.J.,Cardin, C.J.
X-ray Crystal Structures Show DNA Stacking Advantage of Terminal Nitrile Substitution in Ru-dppz Complexes.
Chemistry, 24:15859-15867, 2018

PubMed Abstract: The new complexes [Ru(TAP) (11-CN-dppz)] , [Ru(TAP) (11-Br-dppz)] and [Ru(TAP) (11,12-diCN-dppz)] are reported. The addition of nitrile substituents to the dppz ligand of the DNA photo-oxidising complex [Ru(TAP) (dppz)] promote π-stacking interactions and ordered binding to DNA, as shown by X-ray crystallography. The structure of Λ-[Ru(TAP) (11-CN-dppz)] with the DNA duplex d(TCGGCGCCGA) shows, for the first time with this class of complex, a closed intercalation cavity with an AT base pair at the terminus. The structure obtained is compared to that formed with the 11-Br and 11,12-dinitrile derivatives, highlighting the stabilization of syn guanine by this enantiomer when the terminal base pair is GC. In contrast the AT base pair has the normal Watson-Crick orientation, highlighting the difference in charge distribution between the two purine bases and the complementarity of the dppz-purine interaction. The asymmetry of the cavity highlights the importance of the purine-dppz-purine stacking interaction.

PubMed: 30063271
DOI: 10.1002/chem.201803021

実験手法

X-RAY DIFFRACTION (1.061 Å)