| Literature DB >> 29741793 |
Wojciech Drożdż1,2, Anna Walczak1,2, Yannick Bessin3, Virginie Gervais4, Xiao-Yu Cao5, Jean-Marie Lehn5, Sébastien Ulrich3, Artur R Stefankiewicz1,2.
Abstract
We report the implementation of coordination chemistry onto the generation of new types of metallosupramolecular complexes with laterally appended cationic moieties for DNA binding in buffered aqueous media. Utilization of an N,N,O-type coordination pocket along with an octahedral zinc(II) metal ion allowed us to obtain mono- and tetranuclear complexes in both solution and solid state, as confirmed by NMR spectroscopy and single-crystal X-ray diffraction, respectively. By using isothermal titration calorimetry and gel electrophoresis, multiply charged cationic assemblies were observed to effectively bind to DNA through multivalent electrostatic interactions. Furthermore, we observed a correlation between the multivalency of the compounds employed and the effectiveness of DNA binding.Entities:
Keywords: DNA recognition; coordination chemistry; multivalency; self-assembly; zinc
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Year: 2018 PMID: 29741793 DOI: 10.1002/chem.201801552
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236