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Facile coupling of synthetic peptides and peptide–polymer conjugates to cartilage via transglutaminase enzyme

Paper ID Volume ID Publish Year Pages File Format Full-Text
10465 686 2007 10 PDF Available
Title
Facile coupling of synthetic peptides and peptide–polymer conjugates to cartilage via transglutaminase enzyme
Abstract

Covalent attachment of synthetic and biological molecules to tissue surfaces can be used to enhance local drug delivery, reduce adhesions after surgery, and attach reconstructive biomaterials and tissue-engineered matrices to tissues. We present here a mild approach to coupling polymers to tissue surfaces through an enzyme catalyzed reaction between peptide modified polymer and native protein components of the tissue extracellular matrix (ECM). Tissue transglutaminase (tTG), a Ca2+-dependent enzyme that catalyzes the reaction between lysine and glutamine residues to form a ε(γ-glutaminyl) lysine isopeptide bond, was incubated with cartilage in the presence of lysine (FKG-NH2) and glutamine (GQQQLG-NH2) peptides as well as peptide functionalized poly(ethylene glycol) (PEG). Immunohistochemistry was used to detect the presence of covalently bound PEG polymer at the tissue surface as well as to a depth of as much as 10 μm below the surface. Collagen II, fibronectin, osteopontin and osteonectin were found to react with the peptides and peptide modified PEG in the presence of tTG in solution, suggesting these cartilage ECM components as being substrates in the tissue reaction. The results illustrate the use of tTG as a simple, effective and biologically compatible method of coupling synthetic and biological molecules to cartilage and other tissues containing ECM proteins that are substrates of tTG.

Keywords
Transglutaminase; Cartilage; Peptide; Polymer; Conjugation; Surface
First Page Preview
Facile coupling of synthetic peptides and peptide–polymer conjugates to cartilage via transglutaminase enzyme
Publisher
Database: Elsevier - ScienceDirect
Journal: Biomaterials - Volume 28, Issue 35, December 2007, Pages 5215–5224
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Bioengineering