Biophysical and pharmacological characterization of a full-length synthetic analog of the antitumor polypeptide crotamine

Detalhes bibliográficos
Autor(a) principal: de Carvalho Porta, Lucas
Data de Publicação: 2020
Outros Autores: Fadel, Valmir [UNESP], D’Arc Campeiro, Joana, Oliveira, Eduardo Brandt, Godinho, Rosely Oliveira, Hayashi, Mirian Akemi Furuie
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1007/s00109-020-01975-y
http://hdl.handle.net/11449/201162
Resumo: Abstract: Crotamine is a polypeptide isolated from the venom of a South American rattlesnake. Among the properties and biological activities of crotamine, the most extraordinary is its ability to enter cells with unique selective affinity and cytotoxic activity against actively proliferating cells, such as tumor cells. This peptide is also a cargo carrier, and anticipating commercial application of this native polypeptide as a potential theranostic compound against cancer, we performed here a side-by-side characterization of a chemically synthesized full-length crotamine compared with its native counterpart. The structural, biophysical, and pharmacological properties were evaluated. Comparative NMR studies showed structural conservation of synthetic crotamine. Moreover, similarly to native crotamine, the synthetic polypeptide was also capable of inhibiting tumor growth in vivo, increasing the survival of mice bearing subcutaneous tumor. We also confirmed the ability of synthetic crotamine to transfect and transport DNA into eukaryotic cells, in addition to the importance of proteoglycans on cell surface for its internalization. This work opens new opportunities for future evaluation of chimeric and/or point-mutated analogs of this snake polypeptide, aiming for improving crotamine properties and applications, as well as possibly diminishing its potential toxic effects. Key messages: • Synthetic crotamine showed ex vivo and in vivo activities similar to native peptide. • Synthetic crotamine structure conservation was demonstrated by NMR analysis. • Synthetic crotamine is able to transfect and transport DNA into eukaryotic cells. • Synthetic crotamine shows tumor growth inhibition in vivo. • Synthetic crotamine increases survival of mice bearing tumor.
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spelling Biophysical and pharmacological characterization of a full-length synthetic analog of the antitumor polypeptide crotamineCPPCrotamineHind limb paralysisMelanoma tumorProteoglycansSkeletal muscle contractionStructural NMRAbstract: Crotamine is a polypeptide isolated from the venom of a South American rattlesnake. Among the properties and biological activities of crotamine, the most extraordinary is its ability to enter cells with unique selective affinity and cytotoxic activity against actively proliferating cells, such as tumor cells. This peptide is also a cargo carrier, and anticipating commercial application of this native polypeptide as a potential theranostic compound against cancer, we performed here a side-by-side characterization of a chemically synthesized full-length crotamine compared with its native counterpart. The structural, biophysical, and pharmacological properties were evaluated. Comparative NMR studies showed structural conservation of synthetic crotamine. Moreover, similarly to native crotamine, the synthetic polypeptide was also capable of inhibiting tumor growth in vivo, increasing the survival of mice bearing subcutaneous tumor. We also confirmed the ability of synthetic crotamine to transfect and transport DNA into eukaryotic cells, in addition to the importance of proteoglycans on cell surface for its internalization. This work opens new opportunities for future evaluation of chimeric and/or point-mutated analogs of this snake polypeptide, aiming for improving crotamine properties and applications, as well as possibly diminishing its potential toxic effects. Key messages: • Synthetic crotamine showed ex vivo and in vivo activities similar to native peptide. • Synthetic crotamine structure conservation was demonstrated by NMR analysis. • Synthetic crotamine is able to transfect and transport DNA into eukaryotic cells. • Synthetic crotamine shows tumor growth inhibition in vivo. • Synthetic crotamine increases survival of mice bearing tumor.Departamento de Farmacologia Escola Paulista de Medicina (EPM) Universidade Federal de São Paulo (UNIFESP), Rua 3 de maio 100, Ed. INFAR, 3rd floorUniversidade Estadual de São Paulo (UNESP)Departamento de Bioquímica e Imunologia Universidade de São Paulo (USP-FMRP)Universidade Estadual de São Paulo (UNESP)Universidade Federal de São Paulo (UNIFESP)Universidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)de Carvalho Porta, LucasFadel, Valmir [UNESP]D’Arc Campeiro, JoanaOliveira, Eduardo BrandtGodinho, Rosely OliveiraHayashi, Mirian Akemi Furuie2020-12-12T02:25:37Z2020-12-12T02:25:37Z2020-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1007/s00109-020-01975-yJournal of Molecular Medicine.1432-14400946-2716http://hdl.handle.net/11449/20116210.1007/s00109-020-01975-y2-s2.0-85090310439Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Molecular Medicineinfo:eu-repo/semantics/openAccess2021-10-22T12:11:02Zoai:repositorio.unesp.br:11449/201162Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:05:10.874360Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Biophysical and pharmacological characterization of a full-length synthetic analog of the antitumor polypeptide crotamine
title Biophysical and pharmacological characterization of a full-length synthetic analog of the antitumor polypeptide crotamine
spellingShingle Biophysical and pharmacological characterization of a full-length synthetic analog of the antitumor polypeptide crotamine
de Carvalho Porta, Lucas
CPP
Crotamine
Hind limb paralysis
Melanoma tumor
Proteoglycans
Skeletal muscle contraction
Structural NMR
title_short Biophysical and pharmacological characterization of a full-length synthetic analog of the antitumor polypeptide crotamine
title_full Biophysical and pharmacological characterization of a full-length synthetic analog of the antitumor polypeptide crotamine
title_fullStr Biophysical and pharmacological characterization of a full-length synthetic analog of the antitumor polypeptide crotamine
title_full_unstemmed Biophysical and pharmacological characterization of a full-length synthetic analog of the antitumor polypeptide crotamine
title_sort Biophysical and pharmacological characterization of a full-length synthetic analog of the antitumor polypeptide crotamine
author de Carvalho Porta, Lucas
author_facet de Carvalho Porta, Lucas
Fadel, Valmir [UNESP]
D’Arc Campeiro, Joana
Oliveira, Eduardo Brandt
Godinho, Rosely Oliveira
Hayashi, Mirian Akemi Furuie
author_role author
author2 Fadel, Valmir [UNESP]
D’Arc Campeiro, Joana
Oliveira, Eduardo Brandt
Godinho, Rosely Oliveira
Hayashi, Mirian Akemi Furuie
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Universidade Estadual Paulista (Unesp)
Universidade de São Paulo (USP)
dc.contributor.author.fl_str_mv de Carvalho Porta, Lucas
Fadel, Valmir [UNESP]
D’Arc Campeiro, Joana
Oliveira, Eduardo Brandt
Godinho, Rosely Oliveira
Hayashi, Mirian Akemi Furuie
dc.subject.por.fl_str_mv CPP
Crotamine
Hind limb paralysis
Melanoma tumor
Proteoglycans
Skeletal muscle contraction
Structural NMR
topic CPP
Crotamine
Hind limb paralysis
Melanoma tumor
Proteoglycans
Skeletal muscle contraction
Structural NMR
description Abstract: Crotamine is a polypeptide isolated from the venom of a South American rattlesnake. Among the properties and biological activities of crotamine, the most extraordinary is its ability to enter cells with unique selective affinity and cytotoxic activity against actively proliferating cells, such as tumor cells. This peptide is also a cargo carrier, and anticipating commercial application of this native polypeptide as a potential theranostic compound against cancer, we performed here a side-by-side characterization of a chemically synthesized full-length crotamine compared with its native counterpart. The structural, biophysical, and pharmacological properties were evaluated. Comparative NMR studies showed structural conservation of synthetic crotamine. Moreover, similarly to native crotamine, the synthetic polypeptide was also capable of inhibiting tumor growth in vivo, increasing the survival of mice bearing subcutaneous tumor. We also confirmed the ability of synthetic crotamine to transfect and transport DNA into eukaryotic cells, in addition to the importance of proteoglycans on cell surface for its internalization. This work opens new opportunities for future evaluation of chimeric and/or point-mutated analogs of this snake polypeptide, aiming for improving crotamine properties and applications, as well as possibly diminishing its potential toxic effects. Key messages: • Synthetic crotamine showed ex vivo and in vivo activities similar to native peptide. • Synthetic crotamine structure conservation was demonstrated by NMR analysis. • Synthetic crotamine is able to transfect and transport DNA into eukaryotic cells. • Synthetic crotamine shows tumor growth inhibition in vivo. • Synthetic crotamine increases survival of mice bearing tumor.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-12T02:25:37Z
2020-12-12T02:25:37Z
2020-01-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1007/s00109-020-01975-y
Journal of Molecular Medicine.
1432-1440
0946-2716
http://hdl.handle.net/11449/201162
10.1007/s00109-020-01975-y
2-s2.0-85090310439
url http://dx.doi.org/10.1007/s00109-020-01975-y
http://hdl.handle.net/11449/201162
identifier_str_mv Journal of Molecular Medicine.
1432-1440
0946-2716
10.1007/s00109-020-01975-y
2-s2.0-85090310439
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Molecular Medicine
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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