Selective recognition of A/T-rich DNA 3-way junctions with a three-fold symmetric tripeptide
Jacobo Gómez-González1, Laura Martínez-Castro2, Juan Tolosa-Barrilero3,4
1Centro Singular de Investigación en Química Biolóxica e Materiais Moleculares (CiQUS), Departamento de Química Orgánica, Universidade de Santiago de Compostela, Spain. eugenio.vazquez@usc.es.
Abstract:
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 core.
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