Metal-Based Drug-DNA Interactions and Analytical Determination Methods.

Molecules

Department of Pharmaceutical Biochemistry and Clinical Laboratory, Faculty of Pharmacy, "Iuliu-Hațieganu" University of Medicine and Pharmacy, 400012 Cluj-Napoca, Romania.

Published: September 2024

AI Article Synopsis

  • * Binding mechanisms consist of covalent interactions (irreversible) like cross-linking, and non-covalent interactions (reversible) such as intercalation and groove binding.
  • * The review emphasizes DNA-metal complex interactions and outlines methods currently used to study these interactions.

Article Abstract

DNA structure has many potential places where endogenous compounds and xenobiotics can bind. Therefore, xenobiotics bind along the sites of the nucleic acid with the aim of changing its structure, its genetic message, and, implicitly, its functions. Currently, there are several mechanisms known to be involved in DNA binding. These mechanisms are covalent and non-covalent interactions. The covalent interaction or metal base coordination is an irreversible binding and it is represented by an intra-/interstrand cross-link. The non-covalent interaction is generally a reversible binding and it is represented by intercalation between DNA base pairs, insertion, major and/or minor groove binding, and electrostatic interactions with the sugar phosphate DNA backbone. In the present review, we focus on the types of DNA-metal complex interactions (including some representative examples) and on presenting the methods currently used to study them.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11434005PMC
http://dx.doi.org/10.3390/molecules29184361DOI Listing

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September 2024

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Article Synopsis
  • * Binding mechanisms consist of covalent interactions (irreversible) like cross-linking, and non-covalent interactions (reversible) such as intercalation and groove binding.
  • * The review emphasizes DNA-metal complex interactions and outlines methods currently used to study these interactions.
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