16 research outputs found
Histidine-Based Lipopeptides Enhance Cleavage of Nucleic Acids: Interactions with DNA and Hydrolytic Properties
Interaction studies and cleavage
activity experiments were carried
out between plasmid DNA and a series of histidine-based lipopeptides.
Specific fluorescent probes (ethidium bromide, Hoechst 33342, and
pyrene) were used to monitor intercalation, minor groove binding,
and self-assembly of lipopeptides, respectively. Association between
DNA and lipopeptides was thus evidenced, highlighting the importance of both histidine and
hydrophobic tail in the interaction process. DNA cleavage in the presence
of lipopeptides was then detected by gel electrophoresis and quantified,
showing the importance of histidine and the involvement of its side-chain
imidazole in the hydrolysis mechanism. These systems could then be
developed as synthetic nucleases while raising concern of introducing
histidine in the design of lipopeptide-based transfection vectors
EPR spectroelectrochemical investigation of guanine radical formation and environment effects
Guanine radical detection was carried out by a new convenient and efficient method coupling electron paramagnetic resonance spectroscopy and indirect electro-oxidation of guanine in different biological environments, from the free nucleotide to several types of DNA substrates. Compared to the widely used photoirradiation method, this method appeared more selective in the choice of the electrochemical mediator. Carried out in presence of a ruthenium mediator and PBN as spin trap, this method revealed two types of EPR spectra depending of the environment of the guanine radical. Both EPR spectra show the trapping of the neutral guanine radical G(-H)(center dot) obtained after fast deprotonation of the radical cation G(center dot+). However, they differ by the atom where the trapped radical is centered. This difference highlights the structural dependency of the environment on the nature of the radical formed. This work gave the evidence of an innovative method to detect in situ the guanine radical