International audienceQuinoline-based oligoamide foldamers have been identified as a potent class of G-quadruplex DNA ligands. Their helical structure is thought to target G-quadruplex loops or grooves and not G-tetrads. We report the cocrystal structure of anti-parallel hairpin dimeric DNA G-quadruplex (G4T4G4)2 with a helically folded tetra-quinolinecarboxamide bearing cationic side chain consistent with this hypothesis. Multivalent foldamer-DNA interactions are observed that modify the packing of (G4T4G4)2 in the solid state
The helical duplex architecture of DNA was discovered by Francis Crick and James Watson in 1951 and ...
Intramolecular G-quadruplexes formed by the human telomeric G-rich strand are promising anticancer t...
Guanine-rich nucleic acid sequences have a high propensity to adopt non-B DNA secondary structures l...
Quinoline-based oligoamide foldamers have been identified as a potent class of ligands for G-quadrup...
Human DNA sequences consisting of tandem guanine (G) nucleotides can fold into a four-stranded struc...
G-Quadruplexes are noncanonical structures formed by certain guanine-rich sequences of DNA.1 The G-q...
Guanine-rich oligonucleotides have the ability to adopt non-canonical structures, called G-quadruple...
In a previous work we have demonstrated that the DNA sequence CGGTGGT folds into a higher order G-qu...
G-quadruplexes (G4) are now extensively recognised as a peculiar non-canonical DNA geometry that pla...
Background: DNA-intercalating drugs are planar molecules with several fused aromatic rings that form...
Among non-canonical DNA secondary structures, G-quadruplexes are currently widely studied because of...
There is currently significant interest in the development of G-quadruplex-interactive compounds, gi...
G-rich DNA sequences are able to fold into structures called G-quadruplexes. To obtain general trend...
DNA is the chemotherapeutic target for treating diseases of genetic origin. Besides well-known doubl...
G-quadruplexes are believed to be potential targets for therapeutic intervention and this has result...
The helical duplex architecture of DNA was discovered by Francis Crick and James Watson in 1951 and ...
Intramolecular G-quadruplexes formed by the human telomeric G-rich strand are promising anticancer t...
Guanine-rich nucleic acid sequences have a high propensity to adopt non-B DNA secondary structures l...
Quinoline-based oligoamide foldamers have been identified as a potent class of ligands for G-quadrup...
Human DNA sequences consisting of tandem guanine (G) nucleotides can fold into a four-stranded struc...
G-Quadruplexes are noncanonical structures formed by certain guanine-rich sequences of DNA.1 The G-q...
Guanine-rich oligonucleotides have the ability to adopt non-canonical structures, called G-quadruple...
In a previous work we have demonstrated that the DNA sequence CGGTGGT folds into a higher order G-qu...
G-quadruplexes (G4) are now extensively recognised as a peculiar non-canonical DNA geometry that pla...
Background: DNA-intercalating drugs are planar molecules with several fused aromatic rings that form...
Among non-canonical DNA secondary structures, G-quadruplexes are currently widely studied because of...
There is currently significant interest in the development of G-quadruplex-interactive compounds, gi...
G-rich DNA sequences are able to fold into structures called G-quadruplexes. To obtain general trend...
DNA is the chemotherapeutic target for treating diseases of genetic origin. Besides well-known doubl...
G-quadruplexes are believed to be potential targets for therapeutic intervention and this has result...
The helical duplex architecture of DNA was discovered by Francis Crick and James Watson in 1951 and ...
Intramolecular G-quadruplexes formed by the human telomeric G-rich strand are promising anticancer t...
Guanine-rich nucleic acid sequences have a high propensity to adopt non-B DNA secondary structures l...