Abstract
Reaction of a 17-base hairpin-forming oligonucleotide with [N,N′-bis(salicylaldehyde)- meso-1,2-bis(4-trimethylaminophenyl)ethylenediimino]nickel(II) perchlorate, 2, and KHSO 5 produced two types of high molecular weight products, an alkaline-labile species and a nonalkaline-labile species, which co-migrated on gel electrophoresis. Upon treatment with piperidine, the base-labile derivative led to strand scission products only at accessible guanine residues that were not part of a Watson-Crick duplex. The formation of higher molecular weight species is proposed to occur via a highly reactive ligand-centered radical acting as a DNA alkylating agent.
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