4.7 Article

Study of alkaloid berberine and its interaction with the human telomeric i-motif DNA structure

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.saa.2020.119185

Keywords

Berberine; I-motif; DNA binders; G-quadruplex

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Funding

  1. Spanish Government [PID2019-107158GB-I00, CTQ2017-84415-R]
  2. Italian Government (PIANO DI SOSTEGNO ALLA RICERCA 2018 Linea 2 azione B (DEFENS))
  3. Autonomous Catalan Government [2017SGR114]

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Berberine interacts weakly with the i-motif formed by the human telomere, mainly through electrostatic interactions. The ligand is not selective for i-motif structures, binding equally to folded and unfolded strands without stabilizing the i-motif structure. The development of analytical methods involving fluorescent ligands should consider thermodynamic aspects and selectivity towards different DNA structures.
The alkaloid berberine presents many biological activities related to its potential to bind DNA structures, such as duplex or G-quadruplex. Recently, it has been proposed that berberine may interact with i-motif structures formed from the folding of cytosine-rich sequences. In the present work, the interaction of this alkaloid with the i-motif formed by the human telomere cytosine-rich sequence, as well as with several positive and negative controls, has been studied. Molecular fluorescence and circular dichroism spectroscopies, as well as nuclear magnetic resonance spectrometry and competitive dialysis, have been used with this purpose. The results shown here reveal that the interaction of berberine with this i-motif is weak, mostly electrostatics in nature and takes place with bases not involved in C.C+ base pairs. Moreover, this ligand is not selective for i-motif structures, as binds equally to both, folded structure, and unfolded strand, without producing any stabilization of the i-motif. As a conclusion, the development of analytical methods based on the interaction of fluorescent ligands, such as berberine, with i-motif structures should consider the thermodynamic aspects related with the interaction, as well as the selectivity of the proposed ligands with different DNA structures, including unfolded strands. (C) 2020 Elsevier B.V. All rights reserved.

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