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pubmed-article:11888315pubmed:dateCreated2002-3-12lld:pubmed
pubmed-article:11888315pubmed:abstractTextPoly(OrnGlyGlyOrnGly) was synthesized by classical procedures in solution. The monomeric sequence -OrnGlyGlyOrnGly- was chosen as a modification of -ValGlyGlyValGly-, typical of elastin, to impart primary amine functionality, susceptible to cross-linking with appropriate bifunctional reagents. Herein we focus on the cross-linking of poly(OrnGlyGlyOrnGly) with glutaraldehyde. The polymers, both linear and cross-linked, were characterized and investigated for their molecular and supramolecular properties. Circular dichroism studies performed on linear poly(OrnGlyGlyOrnGly) revealed a variety of conformations similar to elastin. At a supramolecular level, different kinds of aggregates were found such as the elastin-like twisted-rope pattern of filaments and fibrils, together with other specific morphologies, similar to those recently identified in some elastin-mimetic polypeptides.lld:pubmed
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pubmed-article:11888315pubmed:statusMEDLINElld:pubmed
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pubmed-article:11888315pubmed:authorpubmed-author:TamburroA MAMlld:pubmed
pubmed-article:11888315pubmed:authorpubmed-author:MartinyGGlld:pubmed
pubmed-article:11888315pubmed:authorpubmed-author:PerraLLlld:pubmed
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pubmed-article:11888315pubmed:pagination297-304lld:pubmed
pubmed-article:11888315pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:11888315pubmed:articleTitleElastin-based biopolymers: chemical synthesis and structural characterization of linear and cross-linked poly(OrnGlyGlyOrnGly).lld:pubmed
pubmed-article:11888315pubmed:affiliationDepartment of Chemistry, University of Basilicata,Via N. Sauro 85, 85100 Potenza, Italy.lld:pubmed
pubmed-article:11888315pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11888315pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed