In vitro response to functionalized self-assembled peptide scaffolds for three-dimensional cell culture

ABSTRACT Nanomaterials are rich in potential, particularly for the formation of scaffolds that mimic the landscape of the host environment of the cell. This niche arises from the spatial organization of a series of biochemical and biomechanical signals. Self‐assembling peptides have emerged as an im...

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Published in:Biopolymers Vol. 102; no. 2; pp. 197 - 205
Main Authors: Modepalli, Vengama N., Rodriguez, Alexandra L., Li, Rui, Pavuluri, Sivapriya, Nicholas, Kevin R., Barrow, Colin J., Nisbet, David R., Williams, Richard J.
Format: Journal Article
Language:English
Published: United States Blackwell Publishing Ltd 01-03-2014
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Summary:ABSTRACT Nanomaterials are rich in potential, particularly for the formation of scaffolds that mimic the landscape of the host environment of the cell. This niche arises from the spatial organization of a series of biochemical and biomechanical signals. Self‐assembling peptides have emerged as an important tool in the development of functional (bio‐)nanomaterials; these simple, easily synthesized subunits form structures which present the properties of these larger, more complex systems. Scaffolds based upon these nanofibrous matrices are promising materials for regenerative medicine as part of a new methodology in scaffold design where a “bottom‐up” approach is used in order to simulate the native cellular milieu. Importantly, SAPs hold the potential to be bioactive through the presentation of biochemical and biomechanical signals in a context similar to the natural extracellular matrix, making them ideal targets for providing structural and chemical support in a cellular context. Here, we discuss a new methodology for the presentation of biologically relevant epitopes through their effective presentation on the surface of the nanofibers. Here, we demonstrate that these signals have a direct effect on the viability of cells within a three‐dimensional matrix as compared with an unfunctionalized, yet mechanically and morphologically similar system. © 2014 Wiley Periodicals, Inc. Biopolymers (Pept Sci) 102: 197–205, 2014.
Bibliography:istex:24438996452C3A3BE97A5EA3CAB7CE2289C4DCD6
ark:/67375/WNG-R2G592LD-G
ArticleID:BIP22469
Australian Research Council Australian Postdoctoral Fellowship (APD; to DRN)
Alfred Deakin Research Fellowship Scheme
Australian Postgraduate Award (to ALR)
NHMRC Career Development Fellowship - No. APP1050684
Alfred Deakin Research Fellowship (to RJW)
Australian Research Council Discovery Project Scheme - No. DP130103131
Australian Microscopy and Microanalysis Research Facility (AMMRF); access to the facilities of the Centre for Advanced Microscopy (CAM)
This article was originally published online as an accepted preprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office at
biopolymers@wiley.com
ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:0006-3525
2475-8817
1097-0282
2475-8817
DOI:10.1002/bip.22469