Bioorthogonal “Click” Cycloadditions: A Toolkit for Modulating Polymers and Nanostructures in Living Systems

Author:

Lepori Irene1,Oz Yavuz2ORCID,Im Jungkyun34ORCID,Ghosh Nandan3ORCID,Paul Mohuya3ORCID,Schubert Ulrich S.56,Fedeli Stefano56ORCID

Affiliation:

1. Department of Microbiology, University of Massachusetts Amherst, 639 North Pleasant Street, Amherst, MA 01003, USA

2. Department of Chemical and Biomolecular Engineering, University of California Los Angeles, Los Angeles, CA 90095, USA

3. Department of Electronic Materials, Devices, and Equipment Engineering, Soonchunhyang University, Asan 31538, Republic of Korea

4. Department of Chemical Engineering, Soonchunhyang University, Asan 31538, Republic of Korea

5. Laboratory of Organic and Macromolecular Chemistry (IOMC), Friedrich Schiller University Jena, Humboldtstr. 10, 07743 Jena, Germany

6. Jena Center for Soft Matter (JCSM), Friedrich Schiller University Jena, Philosophenweg 7, 07743 Jena, Germany

Abstract

“Click” cycloadditions offer effective pathways for the modifications of supramolecular structures, polymers, and nanomaterials. These reactions include bioorthogonal mechanisms that do not interfere with the biological processes, providing a type of chemistry to operate directly in living environments, such as cells and animals. As a result, the “click” cycloadditions represent highly and selective tools for tailoring the properties of nanomedicine scaffolds, expanding the efficacy of multiple therapeutic strategies. We focused this minireview on the bioorthogonal cycloadditions, presenting an insight into the strategies to modify nanostructured biomedical scaffolds inside living systems. We organized the contributions according to the three main mechanisms of “click” cycloadditions: strain-promoted sydnone-alkyne, tetrazine ligation, and strain-promoted [3+2] azido-alkyne.

Funder

Deutsche Forschungsgemeinschaft

Publisher

MDPI AG

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