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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| 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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| _version_ | 1858435694518599680 |
|---|---|
| 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 |