Biophysical and pharmacological characterization of a full-length synthetic analog of the antitumor polypeptide crotamine
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , |
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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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 |
|
_version_ |
1808128457097347072 |