Issue 18, 2015

Cyclodextrin–peptide conjugates for sequence specific DNA binding

Abstract

Synthetic models of bZIP transcription factors have been developed with the capability of specific DNA recognition. Our design is based on the CuAAC mediated conjugation of basic region Leucine Zipper peptides to different derivatives of α, β and γ-cyclodextrins equipped with azide functionalities. Thorough optimization of reaction conditions allowed convergent and simultaneous conjugation of two long unprotected cationic peptides to cyclodextrin-bis azide derivatives. The resulting constructs were shown to specifically recognize their cognate DNA sequence with nM affinities. In comparison with previously developed TF models, the derivatives described here combine the enhanced DNA binding capabilities with an easy and convergent synthetic route.

Graphical abstract: Cyclodextrin–peptide conjugates for sequence specific DNA binding

Supplementary files

Article information

Article type
Paper
Submitted
27 Mar 2015
Accepted
31 Mar 2015
First published
01 Apr 2015

Org. Biomol. Chem., 2015,13, 5273-5278

Author version available

Cyclodextrin–peptide conjugates for sequence specific DNA binding

Y. Ruiz García, J. Zelenka, Y. V. Pabon, A. Iyer, M. Buděšínský, T. Kraus, C. I. Edvard Smith and A. Madder, Org. Biomol. Chem., 2015, 13, 5273 DOI: 10.1039/C5OB00609K

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