G-Quadruplex Identification in the Genome of Protozoan Parasites Points to Naphthalene Diimide Ligands as New Antiparasitic Agents

  • Efres Belmonte-Reche
  • , Marta Martínez-García
  • , Aurore Guédin
  • , Michela Zuffo
  • , Matilde Arévalo-Ruiz
  • , Filippo Doria
  • , Jenny Campos-Salinas
  • , Marjorie Maynadier
  • , José Juan López-Rubio
  • , Mauro Freccero
  • , Jean Louis Mergny
  • , José María Pérez-Victoria
  • , Juan Carlos Morales

Research output: Contribution to journalArticlepeer-review

Abstract

G-quadruplexes (G4) are DNA secondary structures that take part in the regulation of gene expression. Putative G4 forming sequences (PQS) have been reported in mammals, yeast, bacteria, and viruses. Here, we present PQS searches on the genomes of T. brucei, L. major, and P. falciparum. We found telomeric sequences and new PQS motifs. Biophysical experiments showed that EBR1, a 29 nucleotide long highly repeated PQS in T. brucei, forms a stable G4 structure. G4 ligands based on carbohydrate conjugated naphthalene diimides (carb-NDIs) that bind G4's including hTel could bind EBR1 with selectivity versus dsDNA. These ligands showed important antiparasitic activity. IC 50 values were in the nanomolar range against T. brucei with high selectivity against MRC-5 human cells. Confocal microscopy confirmed these ligands localize in the nucleus and kinetoplast of T. brucei suggesting they can reach their potential G4 targets. Cytotoxicity and zebrafish toxicity studies revealed sugar conjugation reduces intrinsic toxicity of NDIs.

Original languageEnglish
Pages (from-to)1231-1240
Number of pages10
JournalJournal of Medicinal Chemistry
Volume61
Issue number3
DOIs
Publication statusPublished - 8 Feb 2018
Externally publishedYes

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