7NWD
Three-quartet c-kit2 G-quadruplex stabilized by a pyrene conjugate
Summary for 7NWD
Entry DOI | 10.2210/pdb7nwd/pdb |
NMR Information | BMRB: 34611 |
Descriptor | c-kit2_py1, POTASSIUM ION (2 entities in total) |
Functional Keywords | c-kit2, g-quadruplex, pyrene, dna |
Biological source | Homo sapiens |
Total number of polymer chains | 1 |
Total formula weight | 6849.70 |
Authors | Peterkova, K.,Durnik, I.,Marek, R.,Plavec, J.,Podbevsek, P. (deposition date: 2021-03-16, release date: 2021-08-04, Last modification date: 2024-06-19) |
Primary citation | Peterkova, K.,Durnik, I.,Marek, R.,Plavec, J.,Podbevsek, P. c-kit2 G-quadruplex stabilized via a covalent probe: exploring G-quartet asymmetry. Nucleic Acids Res., 49:8947-8960, 2021 Cited by PubMed Abstract: Several sequences forming G-quadruplex are highly conserved in regulatory regions of genomes of different organisms and affect various biological processes like gene expression. Diverse G-quadruplex properties can be modulated via their interaction with small polyaromatic molecules such as pyrene. To investigate how pyrene interacts with G-rich DNAs, we incorporated deoxyuridine nucleotide(s) with a covalently attached pyrene moiety (Upy) into a model system that forms parallel G-quadruplex structures. We individually substituted terminal positions and positions in the pentaloop of the c-kit2 sequence originating from the KIT proto-oncogene with Upy and performed a detailed NMR structural study accompanied with molecular dynamic simulations. Our results showed that incorporation into the pentaloop leads to structural polymorphism and in some cases also thermal destabilization. In contrast, terminal positions were found to cause a substantial thermodynamic stabilization while preserving topology of the parent c-kit2 G-quadruplex. Thermodynamic stabilization results from π-π stacking between the polyaromatic core of the pyrene moiety and guanine nucleotides of outer G-quartets. Thanks to the prevalent overall conformation, our structures mimic the G-quadruplex found in human KIT proto-oncogene and could potentially have antiproliferative effects on cancer cells. PubMed: 34365512DOI: 10.1093/nar/gkab659 PDB entries with the same primary citation |
Experimental method | SOLUTION NMR |
Structure validation
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