Issue 2, 2018

N-Gemini peptides: cytosolic protease resistance via N-terminal dimerization of unstructured peptides

Abstract

Herein we describe a synthetically simple strategy for increasing the lifetime of unstructured peptides in cytosolic environment via dimerization at the N-terminus to block threading into the catalytic cleft of cytosolic proteases. We establish this approach with kinase substrates, allowing for phosphorylation in cells as a demonstration of protease resistance.

Graphical abstract: N-Gemini peptides: cytosolic protease resistance via N-terminal dimerization of unstructured peptides

Supplementary files

Article information

Article type
Communication
Submitted
30 Aug 2017
Accepted
03 Dec 2017
First published
12 Dec 2017

Chem. Commun., 2018,54, 204-207

N-Gemini peptides: cytosolic protease resistance via N-terminal dimerization of unstructured peptides

E. L. Fayer, W. M. Gilliland, J. M. Ramsey, N. L. Allbritton and M. L. Waters, Chem. Commun., 2018, 54, 204 DOI: 10.1039/C7CC06819K

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