DNA-minor-groove-binding ligands are potent antineoplastic molecules. The antibiotic distamycin A is the prototype of one class of these DNA-interfering molecules that have been largely used in vitro. The affinity of distamycin A for DNA is well known, and the structural details of the complexes with some B-DNA and G-quadruplex-forming DNA sequences have been already elucidated. Here, we show that distamycin A binds S100β, a protein involved in the regulation of several cellular processes. The reported affinity of distamycin A for the calcium(II)-loaded S100β reinforces the idea that some biological activities of the DNA-minor-groove-binding ligands arise from the binding to cellular proteins. Copyright © 2015 John Wiley & Sons, Ltd.
Probing the interaction of distamycin A with S100β: the "unexpected" ability of S100β to bind to DNA-binding ligands / Cerofolini, Linda; Amato, Jussara; Borsi, Valentina; Pagano, Bruno; Randazzo, Antonio; Fragai, Marco. - In: JOURNAL OF MOLECULAR RECOGNITION. - ISSN 0952-3499. - STAMPA. - 28:(2015), pp. 376-384. [10.1002/jmr.2452]
Probing the interaction of distamycin A with S100β: the "unexpected" ability of S100β to bind to DNA-binding ligands
CEROFOLINI, LINDA;BORSI, VALENTINA;FRAGAI, MARCO
2015
Abstract
DNA-minor-groove-binding ligands are potent antineoplastic molecules. The antibiotic distamycin A is the prototype of one class of these DNA-interfering molecules that have been largely used in vitro. The affinity of distamycin A for DNA is well known, and the structural details of the complexes with some B-DNA and G-quadruplex-forming DNA sequences have been already elucidated. Here, we show that distamycin A binds S100β, a protein involved in the regulation of several cellular processes. The reported affinity of distamycin A for the calcium(II)-loaded S100β reinforces the idea that some biological activities of the DNA-minor-groove-binding ligands arise from the binding to cellular proteins. Copyright © 2015 John Wiley & Sons, Ltd.File | Dimensione | Formato | |
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