Advanced search×

Understanding the DNA binding of novel non-symmetrical guanidinium/2-aminoimidazolinium derivatives.

Org Biomol Chem 8(24):5558-67 (2010) PMID 20949223

Biophysical studies have been carried out on a family of asymmetric guanidinium-based diaromatic derivatives to assess their potential as DNA minor groove binding agents. To experimentally assess the binding of these compounds to DNA, solution phase biophysical studies have been performed. Thus, surface plasmon resonance, UV-visible spectroscopy and circular and linear dichroism have been utilized to evaluate binding constants, stoichiometry and mode of binding. In addition, the thermodynamics of the binding process have been determined by using isothermal titration calorimetry. These results show significant DNA binding affinity that correlates with the expected 1 : 1 binding ratio usually observed for minor groove binders. Moreover, a simple computational approach has been devised to assess the potential as DNA binders of this family of compounds.

DOI: 10.1039/c0ob00428f
Version: za2963e q8zae q8zb3 q8zc4 q8zd0 q8ze5 q8zf6 q8zg6

Similar articles you may find interesting…

  1. Asymmetrical diaromatic guanidinium/2-aminoimidazolinium derivatives: synthesis and DNA affinity.

    J Med Chem 52(22):7113-21 (2009) PMID 19873979

    We report the synthesis of three families of new amidine-based aromatic derivatives as potential DNA minor groove binding agents for the treatment of cancer. The preparation of monoguanidine, mono-2-aminoimidazoline, and asymmetric diphenylguanidine/2-aminoimidazoline derivatives (compounds 1a-c to...
  2. Application of MDGRAPE-3, a special purpose board for molecular dynamics simulations, to periodic biomolecular systems.

    J Comput Chem 30(1):110-8 (2009) PMID 18524021

    We describe the application of a special purpose board for molecular dynamics simulations, named MDGRAPE-3, to the problem of simulating periodic bio-molecular systems. MDGRAPE-3 is the latest board in a series of hardware accelerators designed to calculate the nonbonding long-range interactions muc...
  3. Using zeta-potential measurements to quantify peptide partition to lipid membranes.

    Eur Biophys J 40(4):481-7 (2011) PMID 21229352

    We derived and tested a mathematical model to determine the K ( p ) from ζ-potential data. The values obtained with this method were compared with those obtained by fluorescence spectroscopy, which is a regular technique used to quantify the interaction of intrinsically fluorescent peptides with se...