Enzymatically-stable oxetane-based dipeptide hydrogels

19Citations
Citations of this article
44Readers
Mendeley users who have this article in their library.

Abstract

Low molecular weight gelators that are not easily degraded by enzymes have a range of potential applications. Here, we report new Fmoc-protected dipeptides in which the amide carbonyl group has been replaced by an oxetane ring. Remarkably one of these peptidomimetics, but not the corresponding dipeptide, is an effective gelator, forming hydrogels at a concentration of 3 mg mL-1. On assembly, there is a lack of beta-sheet structure, implying that there is no requirement for this motif in such a gel. Furthermore, the modified dipeptide is also stable to proteolysis compared to the parent dipeptide.

Cite

CITATION STYLE

APA

McDougall, L., Draper, E. R., Beadle, J. D., Shipman, M., Raubo, P., Jamieson, A. G., & Adams, D. J. (2018). Enzymatically-stable oxetane-based dipeptide hydrogels. Chemical Communications, 54(14), 1793–1796. https://doi.org/10.1039/c7cc09701h

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free