Alkali metal ion concentrations within cells an regulated during the cell c
ycle and may be significantly altered in cancer cells versus normal cells.
Thus, the selective destruction of cancer cells might be achieved by agents
that marry alkali metal ion recognition elements, such as crown ethers, wi
th DNA-cleaving moieties. We have prepared a series of propargylic sulfone-
armed lariat crown ethers, which bind sodium and potassium ions and exhibit
little affinity for lithium ions, as determined by a picrate extraction as
say. We have investigated the supercoiled DNA cleavage efficiency of these
lariat crown ethers in the presence of various alkali metal ions. Monomeric
propargylic sulfone-armed crown ethers 9b and 10b cleave DNA at physiologi
cally relevant pH and exhibit modest increases in DNA cleavage efficiency i
n the presence of potassium and sodium as compared to lithium. In Tris-cont
aining buffer, the monomeric lariat crown ether 10b cleaves DNA in a sodium
ion-dependent fashion, producing 66% more DNA cleavage in the presence of
5.7 mM sodium than in the absence of added sodium. The dimeric propargylic
sulfone-armed lariat crown ether 11 cleaves DNA over 10-fold better in the
presence of potassium than in the presence of lithium. While the level of m
etal ion discrimination exhibited by these compounds is rather modest, they
do represent the first successful attempt to marry molecular recognition o
f specific alkali metal ion with covalent modification of DNA. (C) 2000 Aca
demic Press.