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Crystal structure of Z-DNA in com­plex with the polyamine putrescine and potassium cations at ultra-high resolution

The X-ray crystal structure of the d(CGCGCG)(2)/putrescine(2+)/K(+) com­plex has been determined at 0.60 Å resolution. Stereochemical restraints were used only for the putrescinium dication, and 23 bonds and 18 angles of the Z-DNA nucleotides with dual conformation. The N atoms of the putrescine(2+)...

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Detalles Bibliográficos
Autores principales: Drozdzal, Pawel, Gilski, Miroslaw, Jaskolski, Mariusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8182800/
https://www.ncbi.nlm.nih.gov/pubmed/34096514
http://dx.doi.org/10.1107/S2052520621002663
Descripción
Sumario:The X-ray crystal structure of the d(CGCGCG)(2)/putrescine(2+)/K(+) com­plex has been determined at 0.60 Å resolution. Stereochemical restraints were used only for the putrescinium dication, and 23 bonds and 18 angles of the Z-DNA nucleotides with dual conformation. The N atoms of the putrescine(2+) dication form three direct hydrogen bonds with the N7_G atoms of three different Z-DNA molecules, plus three water-mediated hydrogen bonds with cytosine, guanine and phosphate acceptors. A unique potassium cation was also unambiguously identified in the structure, albeit at a ∼0.5 occupation site shared with a water molecule, providing the first example of such a com­plex with Z-DNA. The K(+) cation has coordination number of eight and an irregular coordination sphere, formed by four water molecules and four O atoms from two phosphate groups of the Z-DNA, including ligands present at fractional occupancy. The structural disorder of the Z-DNA duplex is manifested by the presence of alternate conformations along the DNA backbone. Comparison of the position and interactions of putrescine(2+) in the present structure with other ultra-high-resolution structures of Z-DNA in com­plexes with Mn(2+) and Zn(2+) ions shows that the dicationic putrescinium moiety can effectively substitute these metal ions for stabilization of Z-type DNA duplexes. Furthermore, this comparison also suggests that the spermine(4+) tetracation has a higher affinity for Z-DNA than K(+).