| Literature DB >> 29024239 |
Shu Peng1,2, Andrea Barba-Bon1, Yu-Chen Pan1,2, Werner M Nau1, Dong-Sheng Guo2, Andreas Hennig1.
Abstract
Phosphorylation and dephosphorylation of peptides by kinases and phosphatases is essential for signal transduction in biological systems, and many diseases involve abnormal activities of these enzymes. Herein, we introduce amphiphilic calixarenes as key components for supramolecular, phosphorylation-responsive membrane transport systems. Dye-efflux experiments with liposomes demonstrated that calixarenes are highly active counterion activators for established cell-penetrating peptides, with EC50 values in the low nanomolar range. We have now found that they can even activate membrane transport of short peptide substrates for kinases involved in signal transduction, whereas the respective phosphorylated products are much less efficiently transported. This allows regulation of membrane transport activity by protein kinase A (PKA) and protein kinase C (PKC), as well as monitoring of their activity in a label-free kinase assay.Entities:
Keywords: calixarenes; cell-penetrating peptides; kinases; membrane transport; molecular recognition
Mesh:
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Year: 2017 PMID: 29024239 DOI: 10.1002/anie.201707979
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336