Issue 29, 2012

Bioorthogonal metal-free click-ligation of cRGD-pentapeptide to alginate

Abstract

“Click” reactions have become very common and powerful ligation techniques, of which 1,3-dipolar cycloadditions have most frequently been employed. Since metal-mediated cycloadditions are incompatible in biomedical applications due to toxicity issues associated with transition metals like copper, metal-free variants provide important alternatives. The metal-free conjugation process is studied in detail with special emphasis put on the reaction progress. This report unfolds the first aqueous metal-free “click” conjugation of a cyclic RGD-pentapeptide with the biomacromolecule alginate, creating a “smart” bioactive polymer with potential applications in biomedicine.

Graphical abstract: Bioorthogonal metal-free click-ligation of cRGD-pentapeptide to alginate

Supplementary files

Article information

Article type
Paper
Submitted
22 Mar 2012
Accepted
01 Jun 2012
First published
13 Jun 2012

Org. Biomol. Chem., 2012,10, 5547-5553

Bioorthogonal metal-free click-ligation of cRGD-pentapeptide to alginate

A. Krause, A. Kirschning and G. Dräger, Org. Biomol. Chem., 2012, 10, 5547 DOI: 10.1039/C2OB25604E

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