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 / L., Cerofolini; Amato, Jussara; V., Borsi; Pagano, Bruno; Randazzo, Antonio; M., Fragai. - In: JOURNAL OF MOLECULAR RECOGNITION. - ISSN 0952-3499. - 28:6(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
AMATO, JUSSARA;PAGANO, BRUNO;RANDAZZO, ANTONIO;
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.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.