Progress Toward the Clinical Translation of Bioinspired Peptide and Protein Assemblies
Identifieur interne : 000A73 ( Main/Exploration ); précédent : 000A72; suivant : 000A74Progress Toward the Clinical Translation of Bioinspired Peptide and Protein Assemblies
Auteurs : Kelly M. Hainline ; Chelsea N. Fries ; Joel H. CollierSource :
- Advanced Healthcare Materials [ 2192-2640 ] ; 2017.
Abstract
Supramolecular materials composed of proteins and peptides have been receiving considerable attention toward a range of diseases and conditions from vaccines to drug delivery. Owing to the relative newness of this class of materials, the bulk of work to date has been preclinical. However, examples of approved treatments particularly in vaccines, dentistry, and hemostasis demonstrate the translational potential of supramolecular polypeptides. Critical milestones in the clinical development of this class of materials and currently approved supramolecular polypeptide therapies are described in this study. Additional examples of not‐yet‐approved materials that are steadily advancing toward clinical use are also featured. Spherical assemblies such as virus‐like particles, designed protein nanoparticles, and spherical peptide amphiphiles are highlighted, followed by fiber‐forming systems such as fibrillizing peptides, fiber‐forming peptide‐amphiphiles, and filamentous bacteriophages.
Url:
DOI: 10.1002/adhm.201700930
PubMed: 29115746
PubMed Central: 5858183
Affiliations:
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Le document en format XML
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<p>Supramolecular materials composed of proteins and peptides have been receiving considerable attention toward a range of diseases and conditions from vaccines to drug delivery. Owing to the relative newness of this class of materials, the bulk of work to date has been preclinical. However, examples of approved treatments particularly in vaccines, dentistry, and hemostasis demonstrate the translational potential of supramolecular polypeptides. Critical milestones in the clinical development of this class of materials and currently approved supramolecular polypeptide therapies are described in this study. Additional examples of not‐yet‐approved materials that are steadily advancing toward clinical use are also featured. Spherical assemblies such as virus‐like particles, designed protein nanoparticles, and spherical peptide amphiphiles are highlighted, followed by fiber‐forming systems such as fibrillizing peptides, fiber‐forming peptide‐amphiphiles, and filamentous bacteriophages.</p>
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