Hybridization of complementary and homologous peptide nucleic acid oligomers to a guanine quadruplex-forming RNA.
Ontology highlight
ABSTRACT: Peptide nucleic acid (PNA) oligomers targeted to guanine quadruplex-forming RNAs can be designed in two different ways. First, complementary cytosine-rich PNAs can hybridize by the formation of Watson-Crick base pairs, resulting in hybrid PNA-RNA duplexes. Second, guanine-rich homologous PNAs can hybridize by the formation of G tetrads, resulting in hybrid PNA-RNA quadruplexes. UV thermal denaturation, circular dichroism, and fluorescence spectroscopy experiments were used to compare these two recognition modes and revealed 1:1 duplex formation for the complementary PNA and 2:1 (PNA2-RNA) quadruplex formation for the homologous PNA. Both hybrids were very stable, and hybridization was observed at low nanomolar concentrations. Hybrid quadruplex formation was equally efficient regardless of
SUBMITTER: Marin VL
PROVIDER: S-EPMC2518313 | biostudies-literature | 2006 Feb
REPOSITORIES: biostudies-literature
ACCESS DATA