A DNA-binding copper(I) metallosupramolecular cylinder that acts as an artificial nuclease

被引:52
作者
Childs, Laura J.
Malina, Jaroslav
Rolfsnes, Britt Elin
Pascu, Mirela
Prieto, Maria L.
Broome, Mark L.
Rodger, P. Mark
Sletten, Einar
Moreno, Virtudes [1 ]
Rodger, Alison
Hannon, Michael J.
机构
[1] Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England
[2] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
[3] Dept Quim Inorgan, Barcelona 08028, Spain
[4] Univ Bergen, Dept Chem, N-5007 Bergen, Norway
关键词
artificial nucleases; bioinorganic chemistry; copper; DNA cleavage; supramolecular chemistry;
D O I
10.1002/chem.200600060
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The DNA binding of a dicationic pyridylimine-based dicopper(i) metallosupramolecular cylinder is reported together with its ability to act as an artificial nuclease. The cylinder binds strongly to DNA; more strongly than the spherical dication [Ru(phen)(3)](2+) (phen = 1,10-phenanthroline), but more weakly than the corresponding tetracationic cylinders. DNA coiling effects are not observed with this dication, in contrast to the situation with the previously reported tetracationic cylinder involving a similar ligand. Linear dichroism (LD) data suggests that the dicopper cylinder binds in a different orientation from that of the tetracationic iron cylinder. Furthermore, the dicopper cylinder shows DNA-cleavage activity in the presence of peroxide. Of particular note is that the cylinder displays a marked and unusual ability to cleave both DNA strands at the same site, probably reflecting its dinuclear nature and possibly its mode of binding to the DNA.
引用
收藏
页码:4919 / 4927
页数:9
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