Oligonucleotides 5'-d(CT)(5)-L-d(AG)(5)-L-d(GA)(5)-3' and 5'-d(GA)(5)L
-d(TC)(5)L-d(GA)(5)-3' [L = pO(CH2CH2O)(3)p] were studied by thermal d
enaturation, chemical modification and binding of fluorescent dyes. Bo
th oligonucleotides are shown to fold back on itself twice forming at
pH 7 a sufficiently stable tripler ether with antiparallel-oriented ol
igopurine strands (the first compound) or parallel-oriented oligopurin
e strands (the second compounds). The parallel tripler is significantl
y less stable than the antiparallel one. On the basis of conformationa
l modeling, possible types of base tripling in the triplets are propos
ed. Thus our data provide the first convincingly evidence for the exis
tence of a purine-pyrimidine-purine tripler with parallel orientation
of identical strands.