Substrate specificity of kallikrein-related peptidase 13 activated by salts or glycosaminoglycans and a search for natural substrate candidates

Detalhes bibliográficos
Autor(a) principal: Andrade, Douglas [UNIFESP]
Data de Publicação: 2011
Outros Autores: Assis, Diego Magno [UNIFESP], Santos, Jorge Alexandre Nogueira [UNIFESP], Alves, Fabiana Madureira [UNIFESP], Hirata, Izaura Yoshico [UNIFESP], Araujo, Mariana da Silva [UNIFESP], Blaber, Sachiko I., Blaber, Michael, Juliano, Maria Aparecida [UNIFESP], Juliano, Luiz [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1016/j.biochi.2011.05.037
http://repositorio.unifesp.br/handle/11600/34066
Resumo: KLK13 is a kallikrein-related peptidase preferentially expressed in tonsils, esophagus, testis, salivary glands and cervix. We report the activation of KLK13 by kosmotropic salts and glycosaminoglycans and its substrate specificity by employing a series of five substrates derived from the fluorescence resonance energy transfer (FRET) peptide Abz-KLRSSKQ-EDDnp. KLK13 hydrolyzed all these peptides only at basic residues with highest efficiency for R; furthermore, the S(3) to S(2)' subsites accepted most of the natural amino acids with preference also for basic residues. Using a support-bound FRET peptide library eight peptide substrates were identified containing sequences of proteins found in testis and one with myelin basic protein sequence, each of which was well hydrolyzed by KLK13. Histatins are salivary peptides present in higher primates with broad antifungal and mucosal healing activities that are generated from the hydrolysis from large precursor peptides. KLK13 efficiently hydrolyzed synthetic histatin 3 exclusively at R(25) (DSHAKRHHGYKRKFHEKHHSHRGYR(25)down arrow SNYLYDN) that is the first cleavage observed inside the salivary gland.In conclusion, the observed hydrolytic activities of KLK13 and its co-localization with its activators, glycosaminoglycans in the salivary gland and high concentration of sodium citrate in male reproductive tissues, indicates that KLK13 may play a role in the defense of the upper digestive apparatus and in male reproductive organs. (C) 2011 Elsevier Masson SAS. All rights reserved.
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spelling Substrate specificity of kallikrein-related peptidase 13 activated by salts or glycosaminoglycans and a search for natural substrate candidatesKininProteaseHistatinsKosmotropic saltsMyelin basic proteinKLK13 is a kallikrein-related peptidase preferentially expressed in tonsils, esophagus, testis, salivary glands and cervix. We report the activation of KLK13 by kosmotropic salts and glycosaminoglycans and its substrate specificity by employing a series of five substrates derived from the fluorescence resonance energy transfer (FRET) peptide Abz-KLRSSKQ-EDDnp. KLK13 hydrolyzed all these peptides only at basic residues with highest efficiency for R; furthermore, the S(3) to S(2)' subsites accepted most of the natural amino acids with preference also for basic residues. Using a support-bound FRET peptide library eight peptide substrates were identified containing sequences of proteins found in testis and one with myelin basic protein sequence, each of which was well hydrolyzed by KLK13. Histatins are salivary peptides present in higher primates with broad antifungal and mucosal healing activities that are generated from the hydrolysis from large precursor peptides. KLK13 efficiently hydrolyzed synthetic histatin 3 exclusively at R(25) (DSHAKRHHGYKRKFHEKHHSHRGYR(25)down arrow SNYLYDN) that is the first cleavage observed inside the salivary gland.In conclusion, the observed hydrolytic activities of KLK13 and its co-localization with its activators, glycosaminoglycans in the salivary gland and high concentration of sodium citrate in male reproductive tissues, indicates that KLK13 may play a role in the defense of the upper digestive apparatus and in male reproductive organs. (C) 2011 Elsevier Masson SAS. All rights reserved.Universidade Federal de São Paulo, Escola Paulista Med, Dept Biophys, BR-04044020 São Paulo, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, Dept Biochem, BR-0404420 São Paulo, BrazilFlorida State Univ, Coll Med, Dept Biomed Sci, Tallahassee, FL 32306 USAUniversidade Federal de São Paulo, Escola Paulista Med, Dept Biophys, BR-04044020 São Paulo, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, Dept Biochem, BR-0404420 São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)USPHS/NIHUSPHS/NIH: 1R15NS057771-01Elsevier B.V.Universidade Federal de São Paulo (UNIFESP)Florida State UnivAndrade, Douglas [UNIFESP]Assis, Diego Magno [UNIFESP]Santos, Jorge Alexandre Nogueira [UNIFESP]Alves, Fabiana Madureira [UNIFESP]Hirata, Izaura Yoshico [UNIFESP]Araujo, Mariana da Silva [UNIFESP]Blaber, Sachiko I.Blaber, MichaelJuliano, Maria Aparecida [UNIFESP]Juliano, Luiz [UNIFESP]2016-01-24T14:17:14Z2016-01-24T14:17:14Z2011-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion1701-1709application/pdfhttp://dx.doi.org/10.1016/j.biochi.2011.05.037Biochimie. Paris: Elsevier France-editions Scientifiques Medicales Elsevier, v. 93, n. 10, p. 1701-1709, 2011.10.1016/j.biochi.2011.05.037WOS000295107700009.pdf0300-9084http://repositorio.unifesp.br/handle/11600/34066WOS:000295107700009engBiochimieinfo:eu-repo/semantics/openAccesshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policyreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-31T21:21:17Zoai:repositorio.unifesp.br/:11600/34066Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-31T21:21:17Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Substrate specificity of kallikrein-related peptidase 13 activated by salts or glycosaminoglycans and a search for natural substrate candidates
title Substrate specificity of kallikrein-related peptidase 13 activated by salts or glycosaminoglycans and a search for natural substrate candidates
spellingShingle Substrate specificity of kallikrein-related peptidase 13 activated by salts or glycosaminoglycans and a search for natural substrate candidates
Andrade, Douglas [UNIFESP]
Kinin
Protease
Histatins
Kosmotropic salts
Myelin basic protein
title_short Substrate specificity of kallikrein-related peptidase 13 activated by salts or glycosaminoglycans and a search for natural substrate candidates
title_full Substrate specificity of kallikrein-related peptidase 13 activated by salts or glycosaminoglycans and a search for natural substrate candidates
title_fullStr Substrate specificity of kallikrein-related peptidase 13 activated by salts or glycosaminoglycans and a search for natural substrate candidates
title_full_unstemmed Substrate specificity of kallikrein-related peptidase 13 activated by salts or glycosaminoglycans and a search for natural substrate candidates
title_sort Substrate specificity of kallikrein-related peptidase 13 activated by salts or glycosaminoglycans and a search for natural substrate candidates
author Andrade, Douglas [UNIFESP]
author_facet Andrade, Douglas [UNIFESP]
Assis, Diego Magno [UNIFESP]
Santos, Jorge Alexandre Nogueira [UNIFESP]
Alves, Fabiana Madureira [UNIFESP]
Hirata, Izaura Yoshico [UNIFESP]
Araujo, Mariana da Silva [UNIFESP]
Blaber, Sachiko I.
Blaber, Michael
Juliano, Maria Aparecida [UNIFESP]
Juliano, Luiz [UNIFESP]
author_role author
author2 Assis, Diego Magno [UNIFESP]
Santos, Jorge Alexandre Nogueira [UNIFESP]
Alves, Fabiana Madureira [UNIFESP]
Hirata, Izaura Yoshico [UNIFESP]
Araujo, Mariana da Silva [UNIFESP]
Blaber, Sachiko I.
Blaber, Michael
Juliano, Maria Aparecida [UNIFESP]
Juliano, Luiz [UNIFESP]
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Florida State Univ
dc.contributor.author.fl_str_mv Andrade, Douglas [UNIFESP]
Assis, Diego Magno [UNIFESP]
Santos, Jorge Alexandre Nogueira [UNIFESP]
Alves, Fabiana Madureira [UNIFESP]
Hirata, Izaura Yoshico [UNIFESP]
Araujo, Mariana da Silva [UNIFESP]
Blaber, Sachiko I.
Blaber, Michael
Juliano, Maria Aparecida [UNIFESP]
Juliano, Luiz [UNIFESP]
dc.subject.por.fl_str_mv Kinin
Protease
Histatins
Kosmotropic salts
Myelin basic protein
topic Kinin
Protease
Histatins
Kosmotropic salts
Myelin basic protein
description KLK13 is a kallikrein-related peptidase preferentially expressed in tonsils, esophagus, testis, salivary glands and cervix. We report the activation of KLK13 by kosmotropic salts and glycosaminoglycans and its substrate specificity by employing a series of five substrates derived from the fluorescence resonance energy transfer (FRET) peptide Abz-KLRSSKQ-EDDnp. KLK13 hydrolyzed all these peptides only at basic residues with highest efficiency for R; furthermore, the S(3) to S(2)' subsites accepted most of the natural amino acids with preference also for basic residues. Using a support-bound FRET peptide library eight peptide substrates were identified containing sequences of proteins found in testis and one with myelin basic protein sequence, each of which was well hydrolyzed by KLK13. Histatins are salivary peptides present in higher primates with broad antifungal and mucosal healing activities that are generated from the hydrolysis from large precursor peptides. KLK13 efficiently hydrolyzed synthetic histatin 3 exclusively at R(25) (DSHAKRHHGYKRKFHEKHHSHRGYR(25)down arrow SNYLYDN) that is the first cleavage observed inside the salivary gland.In conclusion, the observed hydrolytic activities of KLK13 and its co-localization with its activators, glycosaminoglycans in the salivary gland and high concentration of sodium citrate in male reproductive tissues, indicates that KLK13 may play a role in the defense of the upper digestive apparatus and in male reproductive organs. (C) 2011 Elsevier Masson SAS. All rights reserved.
publishDate 2011
dc.date.none.fl_str_mv 2011-10-01
2016-01-24T14:17:14Z
2016-01-24T14:17:14Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.biochi.2011.05.037
Biochimie. Paris: Elsevier France-editions Scientifiques Medicales Elsevier, v. 93, n. 10, p. 1701-1709, 2011.
10.1016/j.biochi.2011.05.037
WOS000295107700009.pdf
0300-9084
http://repositorio.unifesp.br/handle/11600/34066
WOS:000295107700009
url http://dx.doi.org/10.1016/j.biochi.2011.05.037
http://repositorio.unifesp.br/handle/11600/34066
identifier_str_mv Biochimie. Paris: Elsevier France-editions Scientifiques Medicales Elsevier, v. 93, n. 10, p. 1701-1709, 2011.
10.1016/j.biochi.2011.05.037
WOS000295107700009.pdf
0300-9084
WOS:000295107700009
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Biochimie
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
eu_rights_str_mv openAccess
rights_invalid_str_mv http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.format.none.fl_str_mv 1701-1709
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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