2'-modified nucleosides for site-specific labeling of oligonucleotides. 2002

Elizabeth S Krider, and Jeremiah E Miller, and Thomas J Meade
Division of Biology and the Beckman Institute, California Institute of Technology, Pasadena, California 91125, USA.

We report the synthesis of 2'-modified nucleosides designed specifically for incorporating labels into oligonucleotides. Conversion of these nucleosides to phosphoramidite and solid support-bound derivatives proceeds in good yield. Large-scale synthesis of 11-mer oligonucleotides possessing the 2'-modified nucleosides is achieved using these derivatives. Thermal denaturation studies indicate that the presence of 2'-modified nucleosides in 11-mer duplexes has minimal destabilizing effects on the duplex structure when the nucleosides are placed at the duplex termini. The powerful combination of phosphoramidite and support-bound derivatives of 2'-modified nucleosides affords the large-scale preparation of an entirely new class of oligonucleotides. The ability to synthesize oligonucleotides containing label attachment sites at 3', intervening, and 5' locations of a duplex is a significant advance in the development of oligonucleotide conjugates.

UI MeSH Term Description Entries
D009691 Nucleic Acid Denaturation Disruption of the secondary structure of nucleic acids by heat, extreme pH or chemical treatment. Double strand DNA is "melted" by dissociation of the non-covalent hydrogen bonds and hydrophobic interactions. Denatured DNA appears to be a single-stranded flexible structure. The effects of denaturation on RNA are similar though less pronounced and largely reversible. DNA Denaturation,DNA Melting,RNA Denaturation,Acid Denaturation, Nucleic,Denaturation, DNA,Denaturation, Nucleic Acid,Denaturation, RNA,Nucleic Acid Denaturations
D009705 Nucleosides Purine or pyrimidine bases attached to a ribose or deoxyribose. (From King & Stansfield, A Dictionary of Genetics, 4th ed) Nucleoside,Nucleoside Analog,Nucleoside Analogs,Analog, Nucleoside,Analogs, Nucleoside
D009841 Oligonucleotides Polymers made up of a few (2-20) nucleotides. In molecular genetics, they refer to a short sequence synthesized to match a region where a mutation is known to occur, and then used as a probe (OLIGONUCLEOTIDE PROBES). (Dorland, 28th ed) Oligonucleotide
D002851 Chromatography, High Pressure Liquid Liquid chromatographic techniques which feature high inlet pressures, high sensitivity, and high speed. Chromatography, High Performance Liquid,Chromatography, High Speed Liquid,Chromatography, Liquid, High Pressure,HPLC,High Performance Liquid Chromatography,High-Performance Liquid Chromatography,UPLC,Ultra Performance Liquid Chromatography,Chromatography, High-Performance Liquid,High-Performance Liquid Chromatographies,Liquid Chromatography, High-Performance
D006358 Hot Temperature Presence of warmth or heat or a temperature notably higher than an accustomed norm. Heat,Hot Temperatures,Temperature, Hot,Temperatures, Hot
D006868 Hydrolysis The process of cleaving a chemical compound by the addition of a molecule of water.
D000345 Affinity Labels Analogs of those substrates or compounds which bind naturally at the active sites of proteins, enzymes, antibodies, steroids, or physiological receptors. These analogs form a stable covalent bond at the binding site, thereby acting as inhibitors of the proteins or steroids. Affinity Labeling Reagents,Labeling Reagents, Affinity,Labels, Affinity,Reagents, Affinity Labeling
D013056 Spectrophotometry, Ultraviolet Determination of the spectra of ultraviolet absorption by specific molecules in gases or liquids, for example Cl2, SO2, NO2, CS2, ozone, mercury vapor, and various unsaturated compounds. (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed) Ultraviolet Spectrophotometry
D013696 Temperature The property of objects that determines the direction of heat flow when they are placed in direct thermal contact. The temperature is the energy of microscopic motions (vibrational and translational) of the particles of atoms. Temperatures

Related Publications

Elizabeth S Krider, and Jeremiah E Miller, and Thomas J Meade
January 2007, Nucleosides, nucleotides & nucleic acids,
Elizabeth S Krider, and Jeremiah E Miller, and Thomas J Meade
January 2007, Chemical communications (Cambridge, England),
Elizabeth S Krider, and Jeremiah E Miller, and Thomas J Meade
August 1987, Bioorganicheskaia khimiia,
Elizabeth S Krider, and Jeremiah E Miller, and Thomas J Meade
January 2002, The Journal of organic chemistry,
Elizabeth S Krider, and Jeremiah E Miller, and Thomas J Meade
March 2012, Chembiochem : a European journal of chemical biology,
Elizabeth S Krider, and Jeremiah E Miller, and Thomas J Meade
January 2007, Nucleosides, nucleotides & nucleic acids,
Elizabeth S Krider, and Jeremiah E Miller, and Thomas J Meade
October 2018, Tetrahedron letters,
Elizabeth S Krider, and Jeremiah E Miller, and Thomas J Meade
January 2007, Current topics in medicinal chemistry,
Elizabeth S Krider, and Jeremiah E Miller, and Thomas J Meade
May 2022, Chemical record (New York, N.Y.),
Copied contents to your clipboard!