DNA as Supramolecular Scaffold for Porphyrin Arrays on the Nanometer Scale
Autor: | Imenne Bouamaied, Nicolas Amiot, Eugen Stulz, Leslie-Anne Fendt, Sandra Thöni |
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Rok vydání: | 2007 |
Předmět: |
Models
Molecular Circular dichroism Porphyrins Stereochemistry Circular Dichroism Supramolecular chemistry DNA Single-Stranded General Chemistry Biochemistry Porphyrin Catalysis Nanostructures Nucleobase chemistry.chemical_compound Crystallography Colloid and Surface Chemistry chemistry Duplex (building) Covalent bond Nanotechnology Nucleic Acid Conformation Spectrophotometry Ultraviolet Nanometre DNA |
Zdroj: | Journal of the American Chemical Society. 129:15319-15329 |
ISSN: | 1520-5126 0002-7863 |
DOI: | 10.1021/ja075711c |
Popis: | Tetraphenyl porphyrin substituted deoxyuridine was used as a building block to create discrete multiporphyrin arrays via site specific incorporation into DNA. The successful covalent attachment of up to 11 tetraphenyl porphyrins in a row onto DNA shows that there is virtually no limitation in the amount of substituents, and the porphyrin arrays thus obtained reach the nanometer scale (approximately 10 nm). The porphyrin substituents are located in the major groove of the dsDNA and destabilize the duplex by deltaT(m) 5-7 degrees C per porphyrin modification. Force-field structure minimization shows that the porphyrins are either in-line with the groove in isolated modifications or aligned parallel to the nucleobases in adjacent modifications. The CD signals of the porphyrins are dominated by a negative peak arising from the intrinsic properties of the building block. In the single strands, the porphyrins induce stabilization of a secondary helical structure which is confined to the porphyrin modified part. This arrangement can be reproduced by force-field minimization and reveals an elongated helical arrangement compared to the double helix of the porphyrin-DNA. This secondary structure is disrupted above approximately 55 degrees C (T(p)) which is shown by various melting experiments. Both absorption and emission spectroscopy disclose electronic interactions between the porphyrin units upon stacking along the outer rim of the DNA leading to a broadening of the absorbance and a quenching of the emission. The single-stranded and double-stranded form show different spectroscopic properties due to the different arrangement of the porphyrins. Above T(p) the electronic properties (absorption and emission) of the porphyrins change compared to room temperature measurements due to the disruption of the porphyrin stacking at high temperature. The covalent attachment of porphyrins to DNA is therefore a suitable way of creating helical stacks of porphyrins on the nanometer scale. |
Databáze: | OpenAIRE |
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