Importance of hydrophobic interactions in the single-chained cationic surfactant-DNA complexation.

Manuel López-López, Pilar López-Cornejo, Victoria Isabel Martín, Francisco José Ostos, Cintia Checa-Rodríguez, Rosario Prados-Carvajal, José Antonio Lebrón, Pablo Huertas, María Luisa Moyá

Journal: Journal of colloid and interface science 2018;521():197-205

PMID: 29571101

Abstract

The goal of this work was to understand the key factors determining the DNA compacting capacity of single-chained cationic surfactants. Fluorescence, zeta potential, circular dichroism, gel electrophoresis and AFM measurements were carried out in order to study the condensation of the nucleic acid resulting from the formation of the surfactant-DNA complexes. The apparent equilibrium binding constant of the surfactants to the nucleic acid, K, estimated from the experimental results obtained in the ethidium bromide competitive binding experiments, can be considered directly related to the ability of a given surfactant as a DNA compacting agent. The plot of ln(K) vs. ln(cmc), cmc being the critical micelle concentration, for all the bromide and chloride surfactants studied, was found to be a reasonably good linear correlation. This result shows that hydrophobic interactions mainly control the surfactant DNA compaction efficiency.

Copyright © 2018 Elsevier Inc. All rights reserved.

Address: Department of Chemical Engineering, Physical Chemistry and Materials Science, Faculty of Experimental Sciences, Campus de El Carmen, Avda. de las Fuerzas Armadas s/n, 21071 Huelva, Spain.; Department of Physical Chemistry, University of Seville, C/ Profesor García González 1, 41012 Seville, Spain.; Department of Genetics, University of Seville and Andalusian Center for Molecular Biology and Regenerative Medicine-CABIMER, University of Seville-CSIC-University Pablo de Olavide, 41092, Spain.; Department of Physical Chemistry, University of Seville, C/ Profesor García González 1, 41012 Seville, Spain. Electronic address: [email protected].

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