4.6 Article

Crossing of the Cystic Barriers of Toxoplasma gondii by the Fluorescent Coumarin Tetra-Cyclopeptide

期刊

MOLECULES
卷 26, 期 24, 页码 -

出版社

MDPI
DOI: 10.3390/molecules26247506

关键词

cyclopeptides; histone deacetylase; Toxoplasma gondii; bradyzoite; cell-permeable agent; molecular dynamics

资金

  1. Agence Nationale de la Recherche (ANR) [ANR-17-EURE-003]
  2. fondation pour le developpement de la chimie des substances naturelles et ses applications Institut de France/Academie des Sciences
  3. CNRS
  4. Rhone-Alpes region [CPER07_13]
  5. Equip@Meso project [ANR-10-EQPX-29-01]
  6. Ceciccluster platform of the PCECIC infrastructure - ICMG
  7. Labex Arcane [ANR-17-EURE-0003]
  8. CBH-EUR-GS [ANR-17-EURE-0003]
  9. Le vivier de la recherche from the Grenoble-Alpes Teaching Hospital
  10. Brazilian agency FAPEMIG
  11. Brazilian agency CNPq
  12. Brazilian agency CAPES

向作者/读者索取更多资源

FR235222 is a natural tetra-cyclopeptide that inhibits histone deacetylases and is effective on mammalian cells and intracellular apicomplexan parasites. It is characterized by a zinc-binding group for binding to histone deacetylases and a cyclic tetrapeptide moiety crucial for cell permeability. The molecule has shown promise for cell penetration and inhibition of histone deacetylases, even in parasite cells.
FR235222 is a natural tetra-cyclopeptide with a strong inhibition effect on histone deacetylases, effective on mammalian cells as well as on intracellular apicomplexan parasites, such as Toxoplasma gondii, in the tachyzoite and bradyzoite stages. This molecule is characterized by two parts: the zinc-binding group, responsible for the binding to the histone deacetylase, and the cyclic tetrapeptide moiety, which plays a crucial role in cell permeability. Recently, we have shown that the cyclic tetrapeptide coupled with a fluorescent diethyl-amino-coumarin was able to maintain properties of cellular penetration on human cells. Here, we show that this property can be extended to the crossing of the Toxoplasma gondii cystic cell wall and the cell membrane of the parasite in its bradyzoite form, while maintaining a high efficacy as a histone deacetylase inhibitor. The investigation by molecular modeling allows a better understanding of the penetration mechanism.

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