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Phage Display to Augment Biomaterial Function

Biomaterial design relies on controlling interactions between materials and their biological environments to modulate the functions of proteins, cells, and tissues. Phage display is a powerful tool that can be used to discover peptide sequences with high affinity for a desired target. When incorpora...

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Detalles Bibliográficos
Autores principales: Davidson, Thomas A., McGoldrick, Samantha J., Kohn, David H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7504225/
https://www.ncbi.nlm.nih.gov/pubmed/32825391
http://dx.doi.org/10.3390/ijms21175994
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author Davidson, Thomas A.
McGoldrick, Samantha J.
Kohn, David H.
author_facet Davidson, Thomas A.
McGoldrick, Samantha J.
Kohn, David H.
author_sort Davidson, Thomas A.
collection PubMed
description Biomaterial design relies on controlling interactions between materials and their biological environments to modulate the functions of proteins, cells, and tissues. Phage display is a powerful tool that can be used to discover peptide sequences with high affinity for a desired target. When incorporated into biomaterial design, peptides identified via phage display can functionalize material surfaces to control the interaction between a biomaterial and its local microenvironment. A targeting peptide has high specificity for a given target, allowing for homing a specific protein, cell, tissue, or other material to a biomaterial. A functional peptide has an affinity for a given protein, cell, or tissue, but also modulates its target’s activity upon binding. Biomaterials can be further enhanced using a combination of targeting and/or functional peptides to create dual-functional peptides for bridging two targets or modulating the behavior of a specific protein or cell. This review will examine current and future applications of phage display for the augmentation of biomaterials.
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spelling pubmed-75042252020-09-24 Phage Display to Augment Biomaterial Function Davidson, Thomas A. McGoldrick, Samantha J. Kohn, David H. Int J Mol Sci Review Biomaterial design relies on controlling interactions between materials and their biological environments to modulate the functions of proteins, cells, and tissues. Phage display is a powerful tool that can be used to discover peptide sequences with high affinity for a desired target. When incorporated into biomaterial design, peptides identified via phage display can functionalize material surfaces to control the interaction between a biomaterial and its local microenvironment. A targeting peptide has high specificity for a given target, allowing for homing a specific protein, cell, tissue, or other material to a biomaterial. A functional peptide has an affinity for a given protein, cell, or tissue, but also modulates its target’s activity upon binding. Biomaterials can be further enhanced using a combination of targeting and/or functional peptides to create dual-functional peptides for bridging two targets or modulating the behavior of a specific protein or cell. This review will examine current and future applications of phage display for the augmentation of biomaterials. MDPI 2020-08-20 /pmc/articles/PMC7504225/ /pubmed/32825391 http://dx.doi.org/10.3390/ijms21175994 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Davidson, Thomas A.
McGoldrick, Samantha J.
Kohn, David H.
Phage Display to Augment Biomaterial Function
title Phage Display to Augment Biomaterial Function
title_full Phage Display to Augment Biomaterial Function
title_fullStr Phage Display to Augment Biomaterial Function
title_full_unstemmed Phage Display to Augment Biomaterial Function
title_short Phage Display to Augment Biomaterial Function
title_sort phage display to augment biomaterial function
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7504225/
https://www.ncbi.nlm.nih.gov/pubmed/32825391
http://dx.doi.org/10.3390/ijms21175994
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