Unknown

Dataset Information

0

Spectroscopic Properties of Two 5'-(4-Dimethylamino)Azobenzene Conjugated G-Quadruplex Forming Oligonucleotides.


ABSTRACT: The synthesis of two 5'-end (4-dimethylamino)azobenzene conjugated G-quadruplex forming aptamers, the thrombin binding aptamer (TBA) and the HIV-1 integrase aptamer (T30695), was performed. Their structural behavior was investigated by means of UV, CD, fluorescence spectroscopy, and gel electrophoresis techniques in K+-containing buffers and water-ethanol blends. Particularly, we observed that the presence of the 5'-(4-dimethylamino)azobenzene moiety leads TBA to form multimers instead of the typical monomolecular chair-like G-quadruplex and almost hampers T30695 G-quadruplex monomers to dimerize. Fluorescence studies evidenced that both the conjugated G-quadruplexes possess unique fluorescence features when excited at wavelengths corresponding to the UV absorption of the conjugated moiety. Furthermore, a preliminary investigation of the trans-cis conversion of the dye incorporated at the 5'-end of TBA and T30695 showed that, unlike the free dye, in K+-containing water-ethanol-triethylamine blend the trans-to-cis conversion was almost undetectable by means of a standard UV spectrophotometer.

SUBMITTER: Imperatore C 

PROVIDER: S-EPMC7582650 | biostudies-literature | 2020 Sep

REPOSITORIES: biostudies-literature

altmetric image

Publications

Spectroscopic Properties of Two 5'-(4-Dimethylamino)Azobenzene Conjugated G-Quadruplex Forming Oligonucleotides.

Imperatore Concetta C   Varriale Antonio A   Rivieccio Elisa E   Pennacchio Angela A   Staiano Maria M   D'Auria Sabato S   Casertano Marcello M   Altucci Carlo C   Valadan Mohammadhassan M   Singh Manjot M   Menna Marialuisa M   Varra Michela M  

International journal of molecular sciences 20200926 19


The synthesis of two 5'-end (4-dimethylamino)azobenzene conjugated G-quadruplex forming aptamers, the thrombin binding aptamer (TBA) and the HIV-1 integrase aptamer (T30695), was performed. Their structural behavior was investigated by means of UV, CD, fluorescence spectroscopy, and gel electrophoresis techniques in K<sup>+</sup>-containing buffers and water-ethanol blends. Particularly, we observed that the presence of the 5'-(4-dimethylamino)azobenzene moiety leads TBA to form multimers instea  ...[more]

Similar Datasets

| S-EPMC6332060 | biostudies-literature
2015-02-05 | E-GEOD-56239 | biostudies-arrayexpress
| S-EPMC2662494 | biostudies-literature
| S-EPMC2796241 | biostudies-literature
2015-02-05 | GSE56239 | GEO
| S-EPMC7144390 | biostudies-literature
| S-EPMC549566 | biostudies-literature
| S-EPMC2732903 | biostudies-literature
| S-EPMC10302603 | biostudies-literature
| S-EPMC6332122 | biostudies-literature