Wydział Chemii

Kamila Stokowa-Sołtys

Nicola Gaggelli

Justyna Nagaj

Wojciech Szczepanik

Jerzy Ciesiołka

Jan Wrzesiński

Agnieszka Górska

Elena Gaggelli

Gianni Valensin

Małgorzata Jeżowska-Bojczuk

2013

Journal of Inorganic Biochemistry

124

26-34

10.1016/j.jinorgbio.2013.03.002

Naukowa

Angielski

Artykuł

Three representatives of the distinct antibiotics groups: amoxicillin, apramycin and ristomycin A were studied regarding their impact on hepatitis D virus (HDV) ribozyme both in the metal-free form and complexed with copper(II) ions. Hence the Cu(II)-ristomycin A complex has been characterized by means of NMR, EPR, CD and UV–visible spectroscopic techniques and its binding pattern has been compared with the coordination modes estimated previously for Cu(II)-amoxicillin and Cu(II)-apramycin complexes. It has thus been found that all three antibiotics bind the Cu(II) ion in a very similar manner, engaging two nitrogen and two oxygen donors into coordination with the square planar symmetry in physiological conditions. All three tested antibiotics were able to inhibit the HDV ribozyme catalysis. However, in the presence of the complexes, the catalytic reactions were almost completely inhibited. It was important therefore to check whether the complexes used in lower concentrations could inhibit the HDV ribozyme catalytic activity, thus creating opportunities for their practical application. It turned out that the complexes used in the concentrations of 50 μM influenced the catalysis much less effectively comparing to the 200 micromolar concentration. The k_obs values were lower than those observed in the control reaction, in the absence of potential inhibitors: 2-fold for amoxicillin, ristomycin A and 3.3-fold for apramycin, respectively.

Ristomycin A, Apramycin, Amoxicillin, Copper(II) complexes, HDV ribozyme, Self-cleavage inhibition

http://dx.doi.org/10.1016/j.jinorgbio.2013.03.002

http://www.elsevier.com