Publication details

Study of interaction of benzo[c]phenanthridine alkaloids with DNA

Authors

PAROULEK Petr RÁJECKÝ Michal PĚNČÍKOVÁ Kristýna TÁBORSKÝ Petr

Year of publication 2014
Type Conference abstract
Citation
Description G-quadruplex (GQ) is one of non-canonical structures of nucleic acids (NA). Structures of intramolecular GQs (formed by only one strand of NA) can be distinguished into two groups according to sequence orientation: parallel and anti-parallel GQs [1]. The effect of selected benzo[c]phenanthridine and protoberberine alkaloids from plants of Papaveraceae family [2] on stability of parallel (sequence from c- kit oncogene promoter) and anti-parallel (human telomeric sequence) GQ was studied. Stabilization (in terms of melting point shifts) of GQs by interaction with macarpine, sanguilutine, sanguinarubine, sanguinarine, chelerythrine and corysamine was followed by UV-vis and CD spectrometry. Results showed that all tested alkaloids except macarpine have a stabilizing effect on human telomeric sequence (?T m = 3-17 °C). Parallel sequence from c-kit oncogene promoter was stabilized by all alkaloids.
Related projects:

You are running an old browser version. We recommend updating your browser to its latest version.

More info

By clicking “Accept Cookies”, you agree to the storing of cookies on your device to enhance site navigation, analyze site usage, and assist in our marketing efforts. Cookie Settings

Necessary Only Accept Cookies