Duplex recognition by oligonucleotides containing 2 '-deoxy-2 '-fluoro-D-arabinose and 2 '-deoxy-2 '-fluoro-D-ribose. Intermolecular 2 '-OH-phosphatecontacts versus sugar puckering in the stabilization of triple-helical complexes
Cj. Wilds et Mj. Damha, Duplex recognition by oligonucleotides containing 2 '-deoxy-2 '-fluoro-D-arabinose and 2 '-deoxy-2 '-fluoro-D-ribose. Intermolecular 2 '-OH-phosphatecontacts versus sugar puckering in the stabilization of triple-helical complexes, BIOCONJ CHE, 10(2), 1999, pp. 299-305
To gain insight into the origins of the large binding affinity of RNA towar
d target duplexes, 2'-deoxy-2'-fluororibonucleic acid (2'F-RNA) and 2'-deox
y-2'-fluoroarabinonucleic acid (2'F-ANA) were tested for their ability to r
ecognize duplex DNA, duplex RNA, and RNA-DNA hybrids. 2'F-RNA, 2'F-ANA, and
the corresponding control single-stranded (ss) DNA strands were shown to f
orm triple-helical complexes only with duplex DNA and hybrid DNA (Pu)-RNA (
Py), but not with duplex RNA and hybrid RNA (Pu)-DNA (Py). In contrast, an
RNA third strand recognized all four possible duplexes (DD, DR, RD, and RR)
as previously demonstrated by Roberts and Crothers [(1992) Science 258, 14
63-1466]. The 2'F-RNA (C3'-endo) strand exhibited significantly reduced aff
inity for duplexes compared to an unmodified RNA (C3'-endo) strand. These f
indings are consistent with the intermolecular 2'-OH-phosphate contact mech
anism proposed by Escude et al. [(1993) Nucleic Acids Res. 24, 5547-5553],
as a ribo 2'-F atom should not interact with a negatively charged phosphate
. In addition, they emphasize the role of the 2'-OH ribose as a general rec
ognition and binding determinant of RNA. The 2'-F arabino modification (2'F
-ANA, C2'-endo) led to a considerable increase in the binding affinity for
duplex DNA, as compared to those of DNA and 2'F-RNA third strands. This is
likely to be the result of a greater population of C2'-endo pucker of the 2
'F-ANA compared to DNA. The enhancement observed for 2'F-ANA strands toward
duplex DNA is comparable to that observed with 2'-OMe RNA. Since 2'F-ANA h
as been shown to be more resistant to nuclease degradation than DNA, these
results are likely to stimulate experimental work on arabinose derivatives
in laboratories concerned with targeting DNA sequences in vivo ("antigene"
strategy).