Potential use of 13-mer peptides based on phospholipase and oligoarginine as leishmanicidal agents

Phospholipase A2 toxins present in snake venoms interact with biological membranes and serve as structural models for the design of small peptides with anticancer, antibacterial and antiparasitic properties. Oligoarginine peptides are capable of increasing cell membrane permeability (cell penetratin...

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主要作者: Mendes, Bruno (author)
其他作者: de Almeida, José R. (author), Nuno Valec, Nuno (author), Gomese, Paula (author), Gadelhaf, Fernanda R. (author), da Silva, Saulo L. (author), Miguel, Danilo C. (author)
格式: article
出版: 2019
主題:
在線閱讀:http://repositorio.ikiam.edu.ec/jspui/handle/RD_IKIAM/316
https://doi.org/10.1016/j.cbpc.2019.108612
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author Mendes, Bruno
author2 de Almeida, José R.
Nuno Valec, Nuno
Gomese, Paula
Gadelhaf, Fernanda R.
da Silva, Saulo L.
Miguel, Danilo C.
author2_role author
author
author
author
author
author
author_facet Mendes, Bruno
de Almeida, José R.
Nuno Valec, Nuno
Gomese, Paula
Gadelhaf, Fernanda R.
da Silva, Saulo L.
Miguel, Danilo C.
author_role author
collection Repositorio Universidad Regional Amazónica
dc.creator.none.fl_str_mv Mendes, Bruno
de Almeida, José R.
Nuno Valec, Nuno
Gomese, Paula
Gadelhaf, Fernanda R.
da Silva, Saulo L.
Miguel, Danilo C.
dc.date.none.fl_str_mv 2019-10-15T14:05:43Z
2019-10-15T14:05:43Z
2019
dc.format.none.fl_str_mv application/pdf
dc.identifier.none.fl_str_mv Mendes, B., Almeida, J. R., Vale, N., Gomes, P., Gadelha, F. R., Da Silva, S. L., & Miguel, D. C. (2019). Potential use of 13-mer peptides based on phospholipase and oligoarginine as leishmanicidal agents. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology, 226(July), 108612. doi.org/10.1016/j.cbpc.2019.108612
http://repositorio.ikiam.edu.ec/jspui/handle/RD_IKIAM/316
https://doi.org/10.1016/j.cbpc.2019.108612
dc.language.none.fl_str_mv en
dc.publisher.none.fl_str_mv Elsevier
dc.rights.none.fl_str_mv Atribución-NoComercial-SinDerivadas 3.0 Estados Unidos de América
http://creativecommons.org/licenses/by-nc-nd/3.0/us/
info:eu-repo/semantics/openAccess
dc.source.none.fl_str_mv reponame:Repositorio Universidad Regional Amazónica
instname:Universidad Regional Amazónica
instacron:IKIAM
dc.subject.none.fl_str_mv Leishmanicidal activity
Oligoarginine
Peptide
Phospholipase
dc.title.none.fl_str_mv Potential use of 13-mer peptides based on phospholipase and oligoarginine as leishmanicidal agents
dc.type.none.fl_str_mv info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
description Phospholipase A2 toxins present in snake venoms interact with biological membranes and serve as structural models for the design of small peptides with anticancer, antibacterial and antiparasitic properties. Oligoarginine peptides are capable of increasing cell membrane permeability (cell penetrating peptides), and for this reason are interesting delivery systems for compounds of pharmacological interest. Inspired by these two families of bioactive molecules, we have synthesized two 13-mer peptides as potential antileishmanial leads gaining insights into structural features useful for the future design of more potent peptides. The peptides included p-Acl, reproducing a natural segment of a Lys49 PLA2 from Agkistrodon contortrix laticinctus snake venom, and its p-AclR7 analogue where all seven lysine residues were replaced by arginines. Both peptides were active against promastigote and amastigote forms of Leishmania (L.) amazonensis and L. (L.) infantum, while displaying low cytotoxicity for primary murine macrophages. Spectrofluorimetric studies suggest that permeabilization of the parasite's cell membrane is the probable mechanism of action of these biomolecules. Relevantly, the engineered peptide p-AclR7 was more active in both life stages of Leishmania and induced higher rates of ethidium bromide incorporation than its native template p-Acl. Taken together, the results suggest that short peptides based on phospholipase toxins are potential scaffolds for development of antileishmanial candidates. Moreover, specific amino acid substitutions, such those herein employed, may enhance the antiparasitic action of these cationic peptides, encouraging their future biomedical applications.
eu_rights_str_mv openAccess
format article
id IKIAM_4973ff2bddbaa3121a33972532c093bb
identifier_str_mv Mendes, B., Almeida, J. R., Vale, N., Gomes, P., Gadelha, F. R., Da Silva, S. L., & Miguel, D. C. (2019). Potential use of 13-mer peptides based on phospholipase and oligoarginine as leishmanicidal agents. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology, 226(July), 108612. doi.org/10.1016/j.cbpc.2019.108612
instacron_str IKIAM
institution IKIAM
instname_str Universidad Regional Amazónica
language_invalid_str_mv en
network_acronym_str IKIAM
network_name_str Repositorio Universidad Regional Amazónica
oai_identifier_str oai:repositorio.ikiam.edu.ec:RD_IKIAM/316
publishDate 2019
publisher.none.fl_str_mv Elsevier
reponame_str Repositorio Universidad Regional Amazónica
repository.mail.fl_str_mv .
repository.name.fl_str_mv Repositorio Universidad Regional Amazónica - Universidad Regional Amazónica
repository_id_str 0
rights_invalid_str_mv Atribución-NoComercial-SinDerivadas 3.0 Estados Unidos de América
http://creativecommons.org/licenses/by-nc-nd/3.0/us/
spelling Potential use of 13-mer peptides based on phospholipase and oligoarginine as leishmanicidal agentsMendes, Brunode Almeida, José R.Nuno Valec, NunoGomese, PaulaGadelhaf, Fernanda R.da Silva, Saulo L.Miguel, Danilo C.Leishmanicidal activityOligoargininePeptidePhospholipasePhospholipase A2 toxins present in snake venoms interact with biological membranes and serve as structural models for the design of small peptides with anticancer, antibacterial and antiparasitic properties. Oligoarginine peptides are capable of increasing cell membrane permeability (cell penetrating peptides), and for this reason are interesting delivery systems for compounds of pharmacological interest. Inspired by these two families of bioactive molecules, we have synthesized two 13-mer peptides as potential antileishmanial leads gaining insights into structural features useful for the future design of more potent peptides. The peptides included p-Acl, reproducing a natural segment of a Lys49 PLA2 from Agkistrodon contortrix laticinctus snake venom, and its p-AclR7 analogue where all seven lysine residues were replaced by arginines. Both peptides were active against promastigote and amastigote forms of Leishmania (L.) amazonensis and L. (L.) infantum, while displaying low cytotoxicity for primary murine macrophages. Spectrofluorimetric studies suggest that permeabilization of the parasite's cell membrane is the probable mechanism of action of these biomolecules. Relevantly, the engineered peptide p-AclR7 was more active in both life stages of Leishmania and induced higher rates of ethidium bromide incorporation than its native template p-Acl. Taken together, the results suggest that short peptides based on phospholipase toxins are potential scaffolds for development of antileishmanial candidates. Moreover, specific amino acid substitutions, such those herein employed, may enhance the antiparasitic action of these cationic peptides, encouraging their future biomedical applications.Elsevier2019-10-15T14:05:43Z2019-10-15T14:05:43Z2019info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfMendes, B., Almeida, J. R., Vale, N., Gomes, P., Gadelha, F. R., Da Silva, S. L., & Miguel, D. C. (2019). Potential use of 13-mer peptides based on phospholipase and oligoarginine as leishmanicidal agents. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology, 226(July), 108612. doi.org/10.1016/j.cbpc.2019.108612http://repositorio.ikiam.edu.ec/jspui/handle/RD_IKIAM/316https://doi.org/10.1016/j.cbpc.2019.108612enAtribución-NoComercial-SinDerivadas 3.0 Estados Unidos de Américahttp://creativecommons.org/licenses/by-nc-nd/3.0/us/info:eu-repo/semantics/openAccessreponame:Repositorio Universidad Regional Amazónicainstname:Universidad Regional Amazónicainstacron:IKIAM2022-06-04T08:04:38Zoai:repositorio.ikiam.edu.ec:RD_IKIAM/316Institucionalhttps://repositorio.ikiam.edu.ec/Universidad públicahttps://www.ikiam.edu.ec/https://repositorio.ikiam.edu.ec/oaiEcuador...opendoar:02022-06-04T08:04:38falseInstitucionalhttps://repositorio.ikiam.edu.ec/Universidad públicahttps://www.ikiam.edu.ec/https://repositorio.ikiam.edu.ec/oai.Ecuador...opendoar:02022-06-04T08:04:38Repositorio Universidad Regional Amazónica - Universidad Regional Amazónicafalse
spellingShingle Potential use of 13-mer peptides based on phospholipase and oligoarginine as leishmanicidal agents
Mendes, Bruno
Leishmanicidal activity
Oligoarginine
Peptide
Phospholipase
status_str publishedVersion
title Potential use of 13-mer peptides based on phospholipase and oligoarginine as leishmanicidal agents
title_full Potential use of 13-mer peptides based on phospholipase and oligoarginine as leishmanicidal agents
title_fullStr Potential use of 13-mer peptides based on phospholipase and oligoarginine as leishmanicidal agents
title_full_unstemmed Potential use of 13-mer peptides based on phospholipase and oligoarginine as leishmanicidal agents
title_short Potential use of 13-mer peptides based on phospholipase and oligoarginine as leishmanicidal agents
title_sort Potential use of 13-mer peptides based on phospholipase and oligoarginine as leishmanicidal agents
topic Leishmanicidal activity
Oligoarginine
Peptide
Phospholipase
url http://repositorio.ikiam.edu.ec/jspui/handle/RD_IKIAM/316
https://doi.org/10.1016/j.cbpc.2019.108612