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Synthetic Mimics of Antimicrobial Peptides—A Versatile Ring‐Opening Metathesis Polymerization Based Platform for the Synthesis of Selective Antibacterial and Cell‐Penetrating Polymers

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Synthetic Mimics of Antimicrobial Peptides—A Versatile Ring‐Opening Metathesis Polymerization Based Platform for the Synthesis of Selective Antibacterial and Cell‐Penetrating Polymers

Auteurs : Karen Lienkamp [États-Unis] ; Gregory Tew [États-Unis]

Source :

RBID : ISTEX:D423D76F99F9713051C0607D4E10544EBCB4BBAC

Abstract

Natural macromolecules exhibit an extensive arsenal of properties, many of which have proven difficult to recapitulate in simpler synthetic systems. Over the last couple of years, foldamers have emerged as one important step toward increased functionality in synthetic systems. While the great majority of work in this area has focused on folded structures, hence the name, more recent progress has centered on polymers that mimic protein function. These efforts have resulted in the design of relatively simple macromolecules; one example are the synthetic mimics of antimicrobial peptides (SMAMPs) that capture the central physicochemical features of their natural archetypes irrespective of the specific folded form. Here we present our recent efforts to create polymers which display biological activity similar to natural proteins, including antimicrobial and cell‐penetrating peptides.
From antimicrobial peptides to biologically active polymers: The design of synthetic mimics of antimicrobial peptides (SMAMPs) that capture the central physicochemical features of their natural archetypes irrespective of the specific folded form is described (see picture). A discussion on recent efforts to create polymers that display biological activity similar to natural proteins, including antimicrobial and cell‐penetrating peptides, is presented

Url:
DOI: 10.1002/chem.200900049

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ISTEX:D423D76F99F9713051C0607D4E10544EBCB4BBAC

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