| Literature DB >> 27505707 |
Takenori Dairaku1,2, Kyoko Furuita3, Hajime Sato4, Jakub Šebera5, Katsuyuki Nakashima6, Jiro Kondo7, Daichi Yamanaka8, Yoshinori Kondo8, Itaru Okamoto9, Akira Ono9, Vladimír Sychrovský10,11, Chojiro Kojima12, Yoshiyuki Tanaka13,14.
Abstract
The structure of an Ag(I) -mediated cytosine-cytosine base pair, C-Ag(I) -C, was determined with NMR spectroscopy in solution. The observation of 1-bond (15) N-(109) Ag J-coupling ((1) J((15) N,(109) Ag): 83 and 84 Hz) recorded within the C-Ag(I) -C base pair evidenced the N3-Ag(I) -N3 linkage in C-Ag(I) -C. The triplet resonances of the N4 atoms in C-Ag(I) -C demonstrated that each exocyclic N4 atom exists as an amino group (-NH2 ), and any isomerization and/or N4-Ag(I) bonding can be excluded. The 3D structure of Ag(I) -DNA complex determined with NOEs was classified as a B-form conformation with a notable propeller twist of C-Ag(I) -C (-18.3±3.0°). The (109) Ag NMR chemical shift of C-Ag(I) -C was recorded for cytidine/Ag(I) complex (δ((109) Ag): 442 ppm) to completed full NMR characterization of the metal linkage. The structural interpretation of NMR data with quantum mechanical calculations corroborated the structure of the C-Ag(I) -C base pair.Entities:
Keywords: DNA; NMR spectroscopy; bioinorganic chemistry; metallo-base-pair; silver
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Year: 2016 PMID: 27505707 DOI: 10.1002/chem.201603048
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236