Phage Display Identified Peptide with Selectivity for Human Osteoarthritic Chondrocytes

Detalhes bibliográficos
Autor(a) principal: Martins, IM
Data de Publicação: 2023
Outros Autores: Canadas, RF, Pereira, H, Azeredo, J, Reis, RL, Oliveira, JM, Azevedo, HS
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/10216/153470
Resumo: Osteoarthritis (OA) is one of the most common joint disorders in western populations, affecting millions of people worldwide and with a rising incidence as life expectancy continues to increase. Current therapies for OA management fail to halt the progressive degradation of articular cartilage, urging the need for more effective therapies to improve function and enhance quality of life. Through phage display technology, biopanning on a heterogenous chondrocyte population isolated from six different OA donors, and using a random 12-amino acid peptide phage library, a cell-binding peptide selective for human OA chondrocytes (GFQMISNNVYMR) is identified. A two-fold increase in fluorescence intensity is observed for OA chondrocytes, compared to normal chondrocytes, when cells were incubated with the identified peptide conjugated to a fluorescent label, being selectively internalized by OA cells. The identified peptide can be further modified and exploited for developing early diagnostic of OA and/or improve drug delivery to target cells through peptide-drug conjugates.
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spelling Phage Display Identified Peptide with Selectivity for Human Osteoarthritic ChondrocytesOsteoarthritisHuman chondrocytesPhage displayPeptidesTargeted therapyDiagnosticOsteoarthritis (OA) is one of the most common joint disorders in western populations, affecting millions of people worldwide and with a rising incidence as life expectancy continues to increase. Current therapies for OA management fail to halt the progressive degradation of articular cartilage, urging the need for more effective therapies to improve function and enhance quality of life. Through phage display technology, biopanning on a heterogenous chondrocyte population isolated from six different OA donors, and using a random 12-amino acid peptide phage library, a cell-binding peptide selective for human OA chondrocytes (GFQMISNNVYMR) is identified. A two-fold increase in fluorescence intensity is observed for OA chondrocytes, compared to normal chondrocytes, when cells were incubated with the identified peptide conjugated to a fluorescent label, being selectively internalized by OA cells. The identified peptide can be further modified and exploited for developing early diagnostic of OA and/or improve drug delivery to target cells through peptide-drug conjugates.Wiley2023-10-122023-10-12T00:00:00Z2023-10-12T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10216/153470eng2366-398710.1002/adtp.202300263Martins, IMCanadas, RFPereira, HAzeredo, JReis, RLOliveira, JMAzevedo, HSinfo:eu-repo/semantics/embargoedAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-29T15:36:09Zoai:repositorio-aberto.up.pt:10216/153470Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T00:27:34.472247Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Phage Display Identified Peptide with Selectivity for Human Osteoarthritic Chondrocytes
title Phage Display Identified Peptide with Selectivity for Human Osteoarthritic Chondrocytes
spellingShingle Phage Display Identified Peptide with Selectivity for Human Osteoarthritic Chondrocytes
Martins, IM
Osteoarthritis
Human chondrocytes
Phage display
Peptides
Targeted therapy
Diagnostic
title_short Phage Display Identified Peptide with Selectivity for Human Osteoarthritic Chondrocytes
title_full Phage Display Identified Peptide with Selectivity for Human Osteoarthritic Chondrocytes
title_fullStr Phage Display Identified Peptide with Selectivity for Human Osteoarthritic Chondrocytes
title_full_unstemmed Phage Display Identified Peptide with Selectivity for Human Osteoarthritic Chondrocytes
title_sort Phage Display Identified Peptide with Selectivity for Human Osteoarthritic Chondrocytes
author Martins, IM
author_facet Martins, IM
Canadas, RF
Pereira, H
Azeredo, J
Reis, RL
Oliveira, JM
Azevedo, HS
author_role author
author2 Canadas, RF
Pereira, H
Azeredo, J
Reis, RL
Oliveira, JM
Azevedo, HS
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Martins, IM
Canadas, RF
Pereira, H
Azeredo, J
Reis, RL
Oliveira, JM
Azevedo, HS
dc.subject.por.fl_str_mv Osteoarthritis
Human chondrocytes
Phage display
Peptides
Targeted therapy
Diagnostic
topic Osteoarthritis
Human chondrocytes
Phage display
Peptides
Targeted therapy
Diagnostic
description Osteoarthritis (OA) is one of the most common joint disorders in western populations, affecting millions of people worldwide and with a rising incidence as life expectancy continues to increase. Current therapies for OA management fail to halt the progressive degradation of articular cartilage, urging the need for more effective therapies to improve function and enhance quality of life. Through phage display technology, biopanning on a heterogenous chondrocyte population isolated from six different OA donors, and using a random 12-amino acid peptide phage library, a cell-binding peptide selective for human OA chondrocytes (GFQMISNNVYMR) is identified. A two-fold increase in fluorescence intensity is observed for OA chondrocytes, compared to normal chondrocytes, when cells were incubated with the identified peptide conjugated to a fluorescent label, being selectively internalized by OA cells. The identified peptide can be further modified and exploited for developing early diagnostic of OA and/or improve drug delivery to target cells through peptide-drug conjugates.
publishDate 2023
dc.date.none.fl_str_mv 2023-10-12
2023-10-12T00:00:00Z
2023-10-12T00:00:00Z
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dc.identifier.uri.fl_str_mv https://hdl.handle.net/10216/153470
url https://hdl.handle.net/10216/153470
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 2366-3987
10.1002/adtp.202300263
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dc.publisher.none.fl_str_mv Wiley
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