Literature DB >> 19851839

Influence of telopeptides, fibrils and crosslinking on physicochemical properties of type I collagen films.

Robin S Walton1, David D Brand, Jan T Czernuszka.   

Abstract

Type I collagen is widely used in various different forms for research and commercial applications. Different forms of collagen may be classified according to their source, extraction method, crosslinking and resultant ultrastructure. In this study, afibrillar and reconstituted fibrillar films, derived from acid soluble and pepsin digested Type I collagen, were analysed using Lateral Force Microscopy (LFM), Fourier Transform Infra-Red Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC) and enzymatic stability assays to asses the influence of telopeptides, fibrils and crosslinking. LFM proved to be a useful technique to confirm an afibrillar/fibrillar ultrastructure and to elucidate fibril diameters. FTIR has proved insensitive to ultrastructural differences involving telopeptides and fibrils. DSC results showed a significant increase in T(d) for crosslinked samples (+22-28 degrees C), and demonstrated that the thermal behaviour of hydrated, afibrillar films is more akin to reconstituted fibrillar films than monomeric solutions. The enzymatic stability assay has provided new evidence to show that afibrillar films of Type I collagen can be significantly more resistant to collagenase (by up to 3.5 times), than reconstituted fibrillar films, as a direct consequence of the different spatial arrangement of collagen molecules. A novel mechanism for this phenomenon is proposed and discussed. Additionally, the presence of telopeptide regions in afibrillar tropocollagen samples has been shown to increase resistance to collagenase by greater than 3.5 times compared to counterpart afibrillar atelocollagen samples. One-factor ANOVA analysis, with Fisher's LSD post-hoc test, confirms these key findings to be of statistical significance (P < 0.05). The profound physicochemical effects of collagen ultrastructure demonstrated in this study reiterates the need for comprehensive materials disclosure and classification when using these biomaterials.

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Year:  2009        PMID: 19851839     DOI: 10.1007/s10856-009-3910-2

Source DB:  PubMed          Journal:  J Mater Sci Mater Med        ISSN: 0957-4530            Impact factor:   3.896


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  13 in total

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Authors:  Giuseppe Tronci; Amanda Doyle; Stephen J Russell; David J Wood
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Journal:  J Mater Sci Mater Med       Date:  2013-02-22       Impact factor: 3.896

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Authors:  B D Walters; J P Stegemann
Journal:  Acta Biomater       Date:  2013-09-06       Impact factor: 8.947

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6.  pH-responsive collagen fibrillogenesis in confined droplets induced by vapour diffusion.

Authors:  Gloria Belén Ramírez-Rodríguez; Michele Iafisco; Anna Tampieri; Jaime Gómez-Morales; José Manuel Delgado-López
Journal:  J Mater Sci Mater Med       Date:  2014-03-21       Impact factor: 3.896

7.  Ca2+ -induced orientation of tandem collagen binding domains from clostridial collagenase ColG permits two opposing functions of collagen fibril formation and retardation.

Authors:  Perry Caviness; Ryan Bauer; Keisuke Tanaka; Katarzyna Janowska; Jeffrey Randall Roeser; Dawn Harter; Jes Sanders; Christopher Ruth; Osamu Matsushita; Joshua Sakon
Journal:  FEBS J       Date:  2018-08-20       Impact factor: 5.542

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Journal:  Biomaterials       Date:  2013-01-23       Impact factor: 12.479

10.  Characterisation of freeze-dried type II collagen and chondroitin sulfate scaffolds.

Authors:  M Tamaddon; R S Walton; D D Brand; J T Czernuszka
Journal:  J Mater Sci Mater Med       Date:  2013-02-08       Impact factor: 3.896

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