Phage Display Identified Peptide with Selectivity for Human Osteoarthritic Chondrocytes

Author:

Martins Ivone M.1234,Canadas Raphaël F.1256,Pereira Hélder127,Azeredo Joana34,Reis Rui L.12,Oliveira Joaquim M.12,Azevedo Helena S.1289ORCID

Affiliation:

1. 3B's Research Group I3Bs—Research Institute on Biomaterials Biodegradables and Biomimetics University of Minho Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine AvePark Parque de Ciência e Tecnologia Zona Industrial da Gandra Barco Guimarães 4805‐017 Portugal

2. ICVS/3B's—PT Government Associate Laboratory Guimarães Braga 4710‐057 Portugal

3. CEB—Centre of Biological Engineering University of Minho Braga 4710‐057 Portugal

4. LABBELS—Associate Laboratory Guimarães Braga Portugal

5. Tech4MED™ R. 25 de Abril, Ronfe Guimarães Braga 4805‐369 Portugal

6. FMUP–Faculdade de Medicina Universidade do Porto Alameda Prof. Hernâni Monteiro Porto 4200‐319 Portugal

7. Orthopedic Department Centro Hospitalar Póvoa de Varzim‐Vila do Conde Largo da Misericórdia Póvoa de Varzim 4490‐421 Portugal

8. i3S—Instituto de Investigação e Inovação em Saúde Universidade do Porto Porto 4200‐135 Portugal

9. INEB—Instituto de Engenharia Biomédica Universidade do Porto Rua Alfredo Allen, 208 Porto 4200‐135 Portugal

Abstract

AbstractOsteoarthritis (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 cartilage function and enhance patient's quality of life. Through phage display technology, biopanning on a population of heterogenous chondrocyte cells isolated from six different OA donors, and using a random 12‐amino acid peptide phage library, a peptide selective for human OA chondrocytes (GFQMISNNVYMR) is identified. A twofold increase in fluorescence intensity is observed for OA chondrocytes, compared to normal chondrocytes, when cells are 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.

Funder

Comissão de Coordenação e Desenvolvimento Regional do Norte

H2020 Spreading Excellence and Widening Participation

Publisher

Wiley

Subject

Pharmacology (medical),Biochemistry (medical),Genetics (clinical),Pharmaceutical Science,Pharmacology,Medicine (miscellaneous)

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