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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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Citations
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Journal ArticleDOI

Self-assembly of palmitoyl lipopeptides used in skin care products

TL;DR: The self-assembly of three cosmetically active peptide amphiphiles used in commercial skin care products is examined to probe the secondary structure, aggregate morphology, and the nanostructure to provide important insights relevant to the role of self-assembled aggregates on the reported collagen-stimulating properties of these PAs.
Journal ArticleDOI

One-Dimensional Supramolecular Nanoplatforms for Theranostics Based on Co-Assembly of Peptide Amphiphiles.

TL;DR: The coassembly of PAs with desirable functions may be a useful strategy for the generation of tailor-made biocompatible nanomaterials.
Journal ArticleDOI

Mechanochemical Encapsulation of Fullerenes in Peptidic Containers Prepared by Dynamic Chiral Self-Sorting and Self-Assembly.

TL;DR: The NMR spectra show the influence of the chiral environment on the symmetry of the fullerene molecules, which results in the differentiation of diastereotopic carbon atoms for C70 , and the X-ray structures provide unique information on the modes of peptide-fullerene interactions.
Journal ArticleDOI

Control of the Handedness of Self-assemblies of Dipeptides by the Chirality of Phenylalanine and Steric Hindrance of Phenylglycine.

TL;DR: Eight dipeptides, composed of phenylalanine and phenylglycine, that are able to self-assemble into twisted nanoribbons in deionized water are synthesized.
Journal ArticleDOI

Peptide Amphiphile Nanostructures for Targeting of Atherosclerotic Plaque and Drug Delivery

TL;DR: Results show that nanofibers functionalized with apolipoprotein‐mimetic peptides may be effective vehicles for intravascular targeted drug delivery to treat atherosclerosis.
References
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Cell attachment activity of fibronectin can be duplicated by small synthetic fragments of the molecule

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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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