Non-canonical DNA structures, particularly 3-way junctions (3WJs) that are transiently formed during DNA replication, have recently emerged as promising chemotherapeutic targets. Here, we describe a new approach to target 3WJs that relies on the cooperative and sequence selective recognition of A/T-rich duplex DNA branches by three AT-Hook peptides attached to a three-fold symmetric and fluorogenic 1,3,5-tristyrylbenzene core2023-07-18S
International audienceThe human genome is replete with repetitive DNA sequences that can fold into t...
Targeting nucleic acids in a structure- or sequence-specific manner with small molecules remains a s...
International audienceTranslocation of DNA and RNA polymerases along their duplex substrates results...
DNA junctions exist at the branch point of three or four DNA duplexes (dsDNA, or B DNA) in hairpin a...
The human genome is replete with repetitive DNA sequences that can fold into thermodynamically stabl...
International audienceThe human genome is replete with repetitive DNA sequences that can fold into t...
International audienceThe human genome is replete with repetitive DNA sequences that can fold into t...
Targeting nucleic acids in a structure- or sequence-specific manner with small molecules remains a s...
International audienceTranslocation of DNA and RNA polymerases along their duplex substrates results...
DNA junctions exist at the branch point of three or four DNA duplexes (dsDNA, or B DNA) in hairpin a...
The human genome is replete with repetitive DNA sequences that can fold into thermodynamically stabl...
International audienceThe human genome is replete with repetitive DNA sequences that can fold into t...
International audienceThe human genome is replete with repetitive DNA sequences that can fold into t...
Targeting nucleic acids in a structure- or sequence-specific manner with small molecules remains a s...
International audienceTranslocation of DNA and RNA polymerases along their duplex substrates results...