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ISBN: 978-83-60043-10-3 - eurobic9

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Eurobic9, 2-6 September, 2008, Wrocław, Poland<br />

P2<strong>10</strong>. Interaction of Cap43 Protein Fragment with Ni(II) and Cu(II) Ions<br />

M.A. Zoroddu a , M. Peana a , and S. Medici a , T. Kowalik-Jankowska b , H. Kozłowski b<br />

a<br />

Department of Chemistry, University of Sassari, Via Vienna 2, 07<strong>10</strong>0, Sassari, Italy<br />

e-mail: zoroddu@uniss.it<br />

b<br />

Faculty of Chemistry, University of Wrocław, 14 Joliot-Curie, 50-3<strong>83</strong> Wrocław, Poland<br />

One of the research topics in our group is protein Cap 43, which seems directly related to the cellular response<br />

after nickel exposure, [1, 2] as well as to a number of cancers.[1, 3] The studies we carried out for several years<br />

started from a small peptide model of Cap 43 and were successively expanded to include a two-<br />

(TRSRSHTSEG-TRSRSHTSEG) and a three-repeated (TRSRSHTSEG-TRSRSHTSEG-TRSRSHTSEG)<br />

monohistidinic decapeptide fragment in its C-terminus.[4-6] Such 20- and 30-amino acid sequences were tested<br />

for Ni(II)- and Cu(II)- coordination at different pH values, by both potentiometry and spectroscopic techniques<br />

(NMR, EPR, UV-Vis, CD). The two metals showed a slightly different behaviour towards coordination, and the<br />

interaction of Cu(II) ions with the two peptides started at pH values lower than those for Ni(II). What appeared<br />

clear was that in both cases each <strong>10</strong>-amino acid fragment TRSRSHTSEG was able to coordinate a single metal<br />

ion to form a square planar 4N {4N} chromophore. The coordination mode involved an imidazole nitrogen from<br />

the His residue, and the amidic nitrogens from His, Ser, and Arg. At high pH values, further deprotonations were<br />

observed for the Cu(II) species.<br />

References:<br />

[1] D. Zhou, K. Salnikow, M. Costa; Cancer Res., 58, 2182 (1998)<br />

[2] K. Salnikow, D. Zhou, T. Kluz, C. Wang, M. Costa, in: Metal and Genetics, (Sarkar Bed), New York, 131<br />

(1999)<br />

[3] K. Salnikow, T. Kluz, M. Costa, Toxicol. Appl. Pharmacol., 160, 127 (1999)<br />

[4] M.A. Zoroddu, T. Kowalik-Jankowska, H. Kozlowski, K. Salnikow, M. Costa, J. Inorg. Biochem., 84, 47<br />

(2001)<br />

[5] M.A. Zoroddu, M. Peana, T. Kowalik-Jankowska, H. Kozlowski, M. Costa, J. Chem. Soc. Dalton Trans., 458<br />

(2002)<br />

[6] M.A. Zoroddu, M. Peana, T. Kowalik-Jankowska, H. Kozlowski, M. Costa, J. Inorg Biochem., 98, 931<br />

(2004)<br />

_____________________________________________________________________<br />

329

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