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

被引:18
作者
Gargallo, R. [1 ]
Avino, A. [2 ]
Eritja, R. [2 ]
Jarosova, P. [3 ]
Mazzini, S. [4 ]
Scaglioni, L. [4 ]
Taborsky, P. [3 ]
机构
[1] Univ Barcelona, Dept Chem Engn & Analyt Chem, Marti & Franques 1, E-08028 Barcelona, Spain
[2] Inst Adv Chem Catalonia IQAC CSIC, CIBER BBN, Jordi Girona 18-26, E-08034 Barcelona, Spain
[3] Masaryk Univ, Dept Chem, Fac Sci, Kamenice 5, Brno 62500, Czech Republic
[4] Univ Milan, Sect Chem & Biomol Sci, Dept Food Environm & Nutr Sci DEFENS, Via Celoria 2, I-20133 Milan, Italy
关键词
Berberine; I-motif; DNA binders; G-quadruplex; G-QUADRUPLEX; PROTOBERBERINE ALKALOIDS; BINDING; ACID; FLUORESCENCE; SEQUENCE; SANGUINARINE; RECOGNITION; STABILITY; MODE;
D O I
10.1016/j.saa.2020.119185
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
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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页数:12
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