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      Synthetic polypeptides: from polymer design to supramolecular assembly and biomedical application

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          Abstract

          This review highlights the recent advances in the chemical design, supramolecular assembly, and biomedical application of synthetic polypeptides from N-carboxyanhydrides.

          Abstract

          Synthetic polypeptides from the ring-opening polymerization of N-carboxyanhydrides (NCAs) are one of the most important biomaterials. The unique features of these synthetic polypeptides, including their chemical diversity of side chains and their ability to form secondary structures, enable their broad applications in the field of gene delivery, drug delivery, bio-imaging, tissue engineering, and antimicrobials. In this review article, we summarize the recent advances in the design of polypeptide-based supramolecular structures, including complexes with nucleic acids, micelles, vesicles, hybrid nanoparticles, and hydrogels. We also highlight the progress in the chemical design of functional polypeptides, which plays a crucial role to manipulate their assembly behaviours and optimize their biomedical performances. Finally, we conclude the review by discussing the future opportunities in this field, including further studies on the secondary structures and cost-effective synthesis of polypeptide materials.

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          Most cited references255

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          Polymer vesicles.

          Vesicles are microscopic sacs that enclose a volume with a molecularly thin membrane. The membranes are generally self-directed assemblies of amphiphilic molecules with a dual hydrophilic-hydrophobic character. Biological amphiphiles form vesicles central to cell function and are principally lipids of molecular weight less than 1 kilodalton. Block copolymers that mimic lipid amphiphilicity can also self-assemble into vesicles in dilute solution, but polymer molecular weights can be orders of magnitude greater than those of lipids. Structural features of vesicles, as well as properties including stability, fluidity, and intermembrane dynamics, are greatly influenced by characteristics of the polymers. Future applications of polymer vesicles will rely on exploiting unique property-performance relations, but results to date already underscore the fact that biologically derived vesicles are but a small subset of what is physically and chemically possible.
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            Design and development of polymers for gene delivery.

            The lack of safe and efficient gene-delivery methods is a limiting obstacle to human gene therapy. Synthetic gene-delivery agents, although safer than recombinant viruses, generally do not possess the required efficacy. In recent years, a variety of effective polymers have been designed specifically for gene delivery, and much has been learned about their structure-function relationships. With the growing understanding of polymer gene-delivery mechanisms and continued efforts of creative polymer chemists, it is likely that polymer-based gene-delivery systems will become an important tool for human gene therapy.
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              Nonviral vectors for gene delivery.

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                Author and article information

                Journal
                CSRVBR
                Chem. Soc. Rev.
                Chem. Soc. Rev.
                Royal Society of Chemistry (RSC)
                0306-0012
                1460-4744
                2017
                2017
                : 46
                : 21
                : 6570-6599
                Affiliations
                [1 ]Department of Materials Science and Engineering
                [2 ]University of Illinois at Urbana-Champaign
                [3 ]Urbana
                [4 ]USA
                [5 ]Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices
                [6 ]School of Materials Science and Chemical Engineering
                [7 ]Department of Chemistry
                [8 ]Institute of Functional Nano & Soft Materials (FUNSOM)
                [9 ]Soochow University
                [10 ]Suzhou 215123
                [11 ]P. R. China
                Article
                10.1039/C7CS00460E
                28944387
                b2358d33-7cd0-4696-8c87-ffbc577b1153
                © 2017
                History

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