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Séminaire Prof. Liliya A. Yatsunyk

Le 30 avril 2019
À 16h30
Salle des Séminaires

16h30, Salle des Séminaires
Mardi 30 Avril

You are cordially invited to the seminar given by:

Prof. Liliya A. Yatsunyk
(Swarthmore College, USA)

"Interactions between G-quadruplex DNA and porphyrin ligands"

 

Homepage: https://www.swarthmore.edu/liliya-yatsunyk

 

Abstract:

Interactions between G-quadruplex DNA and porphyrin ligands

Liliya A. Yatsunyk, Linda Lin

Swarthmore College, 500 College Ave, Swarthmore, PA 19081

 

Non-canonical DNA structures, notably quadruplexes, are gaining popularity because biological evidence suggests that they play their crucial roles in a variety of disease-related biological processes. G-quadruplex DNA structures are composed of planar guanine tetrads which are engaged in effective p-p stacking and are further stabilized by monovalent central cation (e.g. K+ or Na+), Figure 1A. Sequences with G-quadruplex forming potential are present in telomeres and in oncogene promoters, according to bioinformatics studies.

 

 

Figure 1. G-quadruplex DNA and its complex with NMM. (A) The structure of G-tetrad. (B) Crystals of NMM in complex with Tel22. (C) Electron density and the model for Tel22-NMM complex.

 

Here I will discuss our structural and biophysical characterization of a variety of telomeric and oncogene promoter DNA sequences (e.g. human telomeric DNA (Tel22); telomeric DNA from Tetrahymena thermofila (THM); human c-Myc oncogene promoter) in complex with N-methylmesoporphyrin IX (NMM), derivatives of 5,10,15,20-tetra-N-methylpyridyl porphyrin (TMPyP4), and other porphyrins. Due to the excellent optical properties of porphyrins, we investigated their binding to G-quadruplex DNA using UV-vis and fluorescence titrations. We determined stoichiometries for binding events independently via the Job plot method. We obtained thermodynamic parameters via ITC titrations. We crystallized NMM in complex with Tel22 and THM (Figure 1B, C). Our findings are of great importance for the development of new and efficient anticancer.