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Issue 28, 2017
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Exploring the impact of the side-chain length on peptide/RNA binding events

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Abstract

The impact of the amino-acid side-chain length on peptide–RNA binding events has been investigated using HIV-1 Tat derived peptides as ligands and the HIV-1 TAR RNA element as an RNA model. Our studies demonstrate that increasing the length of all peptide side-chains improves unexpectedly the binding affinity (KD) but reduces the degree of compactness of the peptide–RNA complex. Overall, the side-chain length appears to modulate in an unpredictable way the ability of the peptide to compete with the cognate TAR RNA partner. Beyond the establishment of non-intuitive fundamental relationships, our results open up new perspectives in the design of effective RNA ligand competitors, since a large number of them have already been identified but few studies report on the modulation of the biological activity by modifying in the same way the length of all chains connecting RNA recognition motives to the central scaffold of a ligand.

Graphical abstract: Exploring the impact of the side-chain length on peptide/RNA binding events

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Publication details

The article was received on 02 Jun 2017, accepted on 21 Jun 2017 and first published on 21 Jun 2017


Article type: Paper
DOI: 10.1039/C7CP03726K
Citation: Phys. Chem. Chem. Phys., 2017,19, 18452-18460
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    Exploring the impact of the side-chain length on peptide/RNA binding events

    L. Sbicca, A. L. González, A. Gresika, A. Di Giorgio, J. T. Closa, R. E. Tejedor, M. Andréola, S. Azoulay and N. Patino, Phys. Chem. Chem. Phys., 2017, 19, 18452
    DOI: 10.1039/C7CP03726K

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