Anti-Protozoan Activities of Polar Fish-Derived Polyalanine Synthetic Peptides

Author:

Nunes Ellynes Amancio Correia1ORCID,da Silva Maria Cláudia234,Cardoso Marlon Henrique25ORCID,Preza Sergio Leandro Espíndola2ORCID,de Oliveira Lucas Silva678,Frihling Breno Emanuel Farias2,Charneau Sébastien Olivier68ORCID,Grellier Philippe7,Franco Octávio Luiz25ORCID,Migliolo Ludovico129ORCID

Affiliation:

1. Postgraduate Program in Biochemistry, Federal University of Rio Grande do Norte, Natal 59078-900, Brazil

2. S-Inova Biotech, Graduate Program in Biotechnology, Dom Bosco Catholic University, Campo Grande 79117-900, Brazil

3. Department of Biochemistry and Immunology, Faculty of Medicine of Ribeirão Preto, University of São Paulo, Sao Paulo 14040-900, Brazil

4. Laboratory of Research in Virology and Immunology, Institute of Biological and Health Sciences, Federal University of Alagoas, Maceio 57020-600, Brazil

5. Center for Proteomics and Biochemical Analysis, Catholic University of Brasília, Brasilia 71966-700, Brazil

6. Laboratory of Biochemistry and Protein Chemistry, Department of Cell Biology, Institute of Biological Sciences, University of Brasília, Brasilia 73345-010, Brazil

7. UMR 7245 Molécules de Communication et Adaptation des Micro-Organismes, Muséum National d’Histoire Naturelle, CNRS, 75005 Paris, France

8. Graduate Program in Molecular Pathology, University of Brasilia, Brasilia 73345-010, Brazil

9. Postgraduate Program in Cellular and Molecular Biology, Federal University of Paraíba, João Pessoa 58051-900, Brazil

Abstract

Chagas disease, sleeping sickness and malaria are infectious diseases caused by protozoan parasites that kill millions of people worldwide. Here, we performed in vitro assays of Pa-MAP, Pa-MAP1.9, and Pa-MAP2 synthetic polyalanine peptides derived from the polar fish Pleuronectes americanus toward Trypanosoma cruzi, T. brucei gambiense and Plasmodium falciparum activities. We demonstrated that the peptides Pa-MAP1.9 and Pa-MAP2 were effective to inhibit T. brucei growth. In addition, structural analyses using molecular dynamics (MD) studies showed that Pa-MAP2 penetrates deeper into the membrane and interacts more with phospholipids than Pa-MAP1.9, corroborating the previous in vitro results showing that Pa-MAP1.9 acts within the cell, while Pa-MAP2 acts via membrane lysis. In conclusion, polyalanine Pa-MAP1.9 and Pa-MAP2 presented activity against bloodstream forms of T. b. gambiense, thus encouraging further studies on the application of these peptides as a treatment for sleeping sickness.

Funder

CAPES/COFECUB program

FAPDF

CNPq

CAPES/Proex

ProgramaCentelha 2 MS

Publisher

MDPI AG

Subject

Drug Discovery,Pharmacology, Toxicology and Pharmaceutics (miscellaneous),Pharmaceutical Science

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