The association constants (K) of nucleic acid monomers with a series of wat
er-soluble bis-porphyrins (bisMC1, bisMC3, bisMC5, bisMC7, and bisMC11) in
which two porphyrin units were linked by a methylene chain of various lengt
hs were estimated spectrophotometrically. Among the bis-porphyrins. the K v
alues are similar for each nucleic acid monomer, indicating that the bridgi
ng chain length does not affect the association of the bis-porphyrins with
the nucleic acid monomers. The melting curves of poly(dA)-poly(dT) in the p
resence of bisMC3 or bisMC5 were found to be biphasic, suggesting that bisM
C3 and bisMC5 are bound to poly(dA)-poly(dT) with a binding mode different
from the groove binding exhibited by the corresponding porphyrin monomers.
A negative-induced CD peak in the Soret region of bisMC3 and bisMC5 with po
ly(dA)-poly(dT) is observed and the visible spectral changes of bisMC3 and
bisMC5 upon addition of poly(dA)-poly(dT) are accompanied by a large red sh
ift of the Soret band (bisMC3: 21 nm, bisMC5: 23 nm) with substantial hypoc
hromicity (bisMC3: 49%. bisMC5: 40%). Therefore, it is reasonable to conclu
de that both of the porphyrin units of bisMC3 and bisMC5 intercalate into p
oly(dA)-poly(dT). In contrast to poly(dA)poly(dT). the melting curves of po
ly(dA . dT)(2) in the presence of the bis-porphyrins did not show such biph
asic behavior. Together with the CD and visible absorption data, it is cert
ain that these bis-porphyrins do not intercalate into poly(dA . dT)(2). (C)
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