Abstract
We report the design and synthesis of small molecules that exhibit enhanced luminescence in the presence of duplex rather than single-stranded DNA. The local environment presented by a well-known [Ru(dipyrido[3,2-a:2′,3′-c]phenazine)L2]2+-based DNA intercalator was modified by functionalizing the bipyridine ligands with esters and carboxylic acids. By systematically varying the number and charge of the pendant groups, it was determined that decreasing the electrostatic interaction between the intercalator and the anionic DNA backbone reduced single-strand interactions and translated to better duplex specificity. In studying this class of complexes, a single RuII complex emerged that selectively luminesces in the presence of duplex DNA with little to no background from interacting with single-stranded DNA. This complex shows promise as a new dye capable of selectively staining double- versus single-stranded DNA in gel electrophoresis, which cannot be done with conventional SYBR dyes. Enhanced luminescence in the presence of duplex rather than single-stranded DNA was observed for a [Ru(dipyrido[3,2-a:2′,3′-c]phenazine)L2]2+-based DNA intercalator that was specifically modified by functionalizing the bipyridine ligands with esters and carboxylic acids.
Original language | English (US) |
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Pages (from-to) | 10983-10987 |
Number of pages | 5 |
Journal | Chemistry - A European Journal |
Volume | 21 |
Issue number | 31 |
DOIs | |
State | Published - Jul 27 2015 |
Externally published | Yes |
Keywords
- DNA
- bioinorganic chemistry
- gels
- luminescence
- ruthenium
ASJC Scopus subject areas
- General Chemistry
- Catalysis
- Organic Chemistry