4.5 Article

Size matters: DNA binding site kinetics as a function of polyamide size

Journal

BIOCHIMIE
Volume 199, Issue -, Pages 123-129

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biochi.2022.04.010

Keywords

Antiviral; Kinetics; Polyamide; Fluorescence

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This study presents a comparative kinetic analysis of the binding behavior of hairpin polyamides (PAs) with different sizes to DNA. The results reveal complex and distinct association kinetics for PAs of different sizes. The smaller PA6 shows biphasic association kinetics, while the larger PA20 exhibits simpler kinetics. Moreover, as the size of PAs increases, the residence time also increases, which is important for certain biological activities.
Hairpin polyamides (PAs) are remarkable minor groove-binding DNA ligands that demonstrate high affinity and sequence selectivity. Following extensive studies of 6-8 ring hairpin PAs have been more recent descriptions of larger PAs (14 rings or more) and their distinguishing properties and biological activities. However, there are no comparative kinetic studies of PA DNA binding behaviors over a range of PA sizes, making it difficult to understand important structure-activity relationships related to PA size. Described herein is the first comparative kinetic study as a function of hairpin PA size that examines the complexities of PA-DNA binding behaviors with unprecedented detail. DNA binding kinetics of PAs with 6 (PA6) and 20 (PA20) rings are extensively characterized by fluorescence spectroscopy, and the properties compared with those of 8 and 14 ring hairpin PAs. PA6 has a 1:1 binding site stoichiometry but exhibits biphasic association kinetics, consistent with populating more than one binding mode. One decay constant is at the diffusion controlled limit, and the other is 400-fold slower. In contrast, PA20 has high binding site stoichiometry (2.5:1) but displays a much simpler association kinetic trace with a decay constant of 1-6 M(-1)s(-1). Due to the variability and complexity of association kinetics, it is difficult to identify trends in this behavior as a function of PA size. However, even though hairpin PAs of 8 or more rings bind DNA with similar affinities, residence times increase as PA size increases, ranging from 20 s to over 2500 s. Particularly compelling is that the antiviral PA20 shows little to no dissociation from DNA when challenged with competitor DNA, suggesting that high residence times are important for this biological activity. (C) 2022 Elsevier B.V. and Societe Francaise de Biochimie et Biologie Moleculaire (SFBBM). All rights reserved.

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