Bioconjugate Chemistry · 2014 · 30 citations · 56 references
Life SciencesBiochemistryMolecular BiologyNucleic Acid BiochemistryNucleic Acid ChemistrySupramolecular ChemistryBase PairingBase StackingDna AssemblyDna ChemistryDna StructureMacromolecular AssemblyAggregationDna Double HelixDna Duplex StabilityDuplex StabilityFluorescence QuenchingMolecular HybridsOligonucleotide AssemblyOligonucleotide Hybridization
Double stranded DNA hybrids containing up to four consecutive, face-to-face stacked porphyrins are described. Non-nucleosidic, 5,15-bisphenyl-substituted porphyrin building blocks were incorporated into complementary oligonucleotide strands. Upon hybridization multiple porphyrins are well accommodated inside the DNA scaffold without disturbing the overall B-DNA structure. The formation of double strands containing up to four free base porphyrins is enabled without compromising duplex stability. UV/vis, fluorescence, and CD spectroscopy demonstrate the formation of porphyrins H-aggregates inside the DNA double helix and provide evidence for the existence of strong excitonic coupling between interstrand stacked porphyrins. H-aggregation results in considerable fluorescence quenching. Most intense CD effects are observed in stacks containing four porphyrins. The findings demonstrate the value of DNA for the controlled formation of molecularly defined porphyrin aggregates.
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The native architecture of a photosynthetic membrane
S. Bahatyrova, Raoul N. Frese, C. Alistair Siebert et al. · Nature · 2004 · 453 citations
Fluorescent H‐Aggregates of Merocyanine Dyes
Ulrich Rösch, Sheng Yao, Rüdiger Wortmann et al. · Angewandte Chemie International Edition · 2006 · 400 citations
Natural Sciences, Chemistry, Physics +17