Triplex formation at single-stranded nucleic acid target sites of unrestricted sequence by two added strands of oligonucleotides: A proposed model
- John Hopkins Univ., Baltimore, MD (United States)
By using the standard purine nucleosides, guanosine and adenosine, and the pyrimidine C-nucleosides, pseudoisocytidine and pseudouridine, as complements on a probe strand, it is possible to construct a regular Watson-Crick helix with a single-stranded target sequence having any arrangement of the four naturally-occurring bases found in nucleic acids. The major groove of this helix will have a unique configuration of hydrogen-bonding sites on the probe strand for each of these four base pairs. By using this duplex as a framework, an ensemble of recognition patterns composed of base triads may be constructed. In these patterns, either a homopyrimidine or homopurine third strand binds in the major groove of the duplex formed by the target and probe strands. Ten distinct geometries, or motifs, are shown, each one consisting of four isomorphic base triads built upon recognition of C, G, A, or U(T) residues in the target strand. In order to maintain specific hydrogen bonding and to construct isomorphous triads, the use of several nonstandard bases is proposed. 33 refs., 9 figs., 3 tabs.
- DOE Contract Number:
- FG02-88ER60636
- OSTI ID:
- 6735921
- Journal Information:
- Journal of the American Chemical Society; (United States), Vol. 116:23; ISSN 0002-7863
- Country of Publication:
- United States
- Language:
- English
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ORGANIC
PHYSICAL AND ANALYTICAL CHEMISTRY
59 BASIC BIOLOGICAL SCIENCES
NUCLEIC ACIDS
MOLECULAR STRUCTURE
ADENOSINE
BASES
CHEMICAL BONDS
GUANOSINE
OLIGONUCLEOTIDES
PURINES
PYRIMIDINES
SIMULATION
AROMATICS
AZAARENES
AZINES
DNA
HETEROCYCLIC COMPOUNDS
NUCLEOSIDES
NUCLEOTIDES
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
RIBOSIDES
400201* - Chemical & Physicochemical Properties
550200 - Biochemistry