Substrate specificity of kallikrein-related peptidase 13 activated by salts or glycosaminoglycans and a search for natural substrate candidates
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , , , , , |
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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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 |
_version_ |
1814268429055557632 |