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Open AccessJournal ArticleDOI

Self‐assembly of peptide amphiphiles: From molecules to nanostructures to biomaterials

Honggang Cui, +2 more
- 01 Jan 2010 - 
- Vol. 94, Iss: 1, pp 1-18
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TLDR
The strategies for using molecular self‐assembly as a toolbox to produce peptide amphiphile nanostructures and materials are highlighted and efforts to translate this technology into applications as therapeutics are reviewed.
Abstract
Peptide amphiphiles are a class of molecules that combine the structural features of amphiphilic surfactants with the functions of bioactive peptides and are known to assemble into a variety of nanostructures. A specific type of peptide amphiphiles are known to self-assemble into one-dimensional nanostructures under physiological conditions, predominantly nanofibers with a cylindrical geometry. The resultant nanostructures could be highly bioactive and are of great interest in many biomedical applications, including tissue engineering, regenerative medicine, and drug delivery. In this context, we highlight our strategies for using molecular self-assembly as a toolbox to produce peptide amphiphile nanostructures and materials and efforts to translate this technology into applications as therapeutics. We also review our recent progress in using these materials for treating spinal cord injury, inducing angiogenesis, and for hard tissue regeneration and replacement.

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Formation and Controlled Drug Release Using a Three-Component Supramolecular Hydrogel for Anti- Schistosoma Japonicum Cercariae.

TL;DR: Experimental results indicated that the drug-loaded hydrogels show large drug loadings, long-term release time and relatively higher efficiency to anti-cercariae in the water environment.
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Phosphobisaromatic motifs enable rapid enzymatic self-assembly and hydrogelation of short peptides.

TL;DR: In this article, the first example of phosphonaphthyl (pNP) motifs acting as faster enzymatic triggers than phosphotyrosine for EISA and hydrogelation was presented.
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Self-assembly of model short triblock amphiphiles in dilute solution

TL;DR: A molecular theory is used to study the self-assembly of short diblock and triblock amphiphiles, with head-tail and head-linker-tail structures, to predict the occurrence of a transition from micelle to fiber to lamella when increasing the length of the tail or the linker blocks.
Journal ArticleDOI

The impact of metal coordination on the assembly of bis(indolyl)methane-naphthalene-diimide amphiphiles.

TL;DR: The self-assembly and coordination of amphiphiles comprised of naphthalenediimide and bis(indolyl)methane (BIM) chromophores were investigated as a function of pH and metal and a reorganization from nanotubes to vesicular structures was observed.
References
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Cell attachment activity of fibronectin can be duplicated by small synthetic fragments of the molecule

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PatentDOI

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TL;DR: In this paper, pH-induced self-assembly of a peptide-amphiphile was used to make a nanostructured fibrous scaffold reminiscent of extracellular matrix.
Journal ArticleDOI

Regeneration beyond the glial scar

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Journal ArticleDOI

Selective Differentiation of Neural Progenitor Cells by High-Epitope Density Nanofibers

TL;DR: The artificial nanofiber scaffold induced very rapid differentiation of cells into neurons, while discouraging the development of astrocytes, linked to the amplification of bioactive epitope presentation to cells by the nanofibers.
Journal ArticleDOI

Peptide-amphiphile nanofibers: A versatile scaffold for the preparation of self-assembling materials

TL;DR: The scope of amino acid selection and alkyl tail modification in the peptide-amphiphile molecules are investigated, yielding nanofibers varying in morphology, surface chemistry, and potential bioactivity, demonstrating the chemically versatile nature of this supramolecular system.
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