Literature DB >> 1772569

Phosphorothioate oligonucleotides: chemistry, purification, analysis, scale-up and future directions.

G Zon1, T G Geiser.   

Abstract

There is widespread and growing interest in the use of phosphorothioate-modified oligonucleotides as sequence-specific agents to control transcription, splicing, translation and other regulated processes in vitro and in vivo, as pharmaceuticals. These exciting applications are predicated on the resistance of phosphorothioate oligonucleotides to degradation by nucleases, a property that results simply from incorporation of sulfur into the phosphate backbone. The popularity of phosphorothioate oligonucleotide analogs derives from several of their features: relatively easy automated synthesis, uncomplicated purification and handling, plus high solubility in water. Presented here are current preparative and analytical methods, together with a comprehensive comparative analysis of solid-phase and solution processes for manufacturing phosphorothioate oligonucleotides as bulk pharmaceutical compounds for clinical evaluation. A prospective view of the future is offered with the hope of directing attention to important areas of needed research dealing with phosphorothioate oligonucleotide technology in particular, and manufacturing of nucleic acid pharmaceuticals in general.

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Year:  1991        PMID: 1772569

Source DB:  PubMed          Journal:  Anticancer Drug Des        ISSN: 0266-9536


  14 in total

1.  Construction and selection of bead-bound combinatorial oligonucleoside phosphorothioate and phosphorodithioate aptamer libraries designed for rapid PCR-based sequencing.

Authors:  Xianbin Yang; Suzanne E Bassett; Xin Li; Bruce A Luxon; Norbert K Herzog; Robert E Shope; Judy Aronson; Tarl W Prow; James F Leary; Romy Kirby; Andrew D Ellington; David G Gorenstein
Journal:  Nucleic Acids Res       Date:  2002-12-01       Impact factor: 16.971

Review 2.  In vitro selection using modified or unnatural nucleotides.

Authors:  Scott M Knudsen; Michael P Robertson; Andrew D Ellington
Journal:  Curr Protoc Nucleic Acid Chem       Date:  2002-02

Review 3.  Application of antisense DNA method for the study of molecular bases of brain function and behavior.

Authors:  S Ogawa; D W Pfaff
Journal:  Behav Genet       Date:  1996-05       Impact factor: 2.805

4.  Mechanism of oligonucleotide release from cationic liposomes.

Authors:  O Zelphati; F C Szoka
Journal:  Proc Natl Acad Sci U S A       Date:  1996-10-15       Impact factor: 11.205

5.  Intracellular distribution and mechanism of delivery of oligonucleotides mediated by cationic lipids.

Authors:  O Zelphati; F C Szoka
Journal:  Pharm Res       Date:  1996-09       Impact factor: 4.200

Review 6.  Brief overview of control of genetic expression by antisense oligonucleotides and in vivo applications. Prospects for neurobiology.

Authors:  G Zon
Journal:  Mol Neurobiol       Date:  1995 Apr-Jun       Impact factor: 5.590

7.  Inhibition of Rev activity and human immunodeficiency virus type 1 replication by antisense oligodeoxynucleotide phosphorothioate analogs directed against the Rev-responsive element.

Authors:  G Li; J Lisziewicz; D Sun; G Zon; S Daefler; F Wong-Staal; R C Gallo; M E Klotman
Journal:  J Virol       Date:  1993-11       Impact factor: 5.103

8.  Intracellular oligonucleotide hybridization detected by fluorescence resonance energy transfer (FRET).

Authors:  S Sixou; F C Szoka; G A Green; B Giusti; G Zon; D J Chin
Journal:  Nucleic Acids Res       Date:  1994-02-25       Impact factor: 16.971

9.  Apoptosis of human BEL-7402 hepatocellular carcinoma cells released by antisense H-ras DNA--in vitro and in vivo studies.

Authors:  Y Liao; Z Y Tang; K D Liu; S L Ye; Z Huang
Journal:  J Cancer Res Clin Oncol       Date:  1997       Impact factor: 4.553

10.  Analysis of oligo(deoxynucleoside phosphorothioate)s and their diastereomeric composition.

Authors:  A Wilk; W J Stec
Journal:  Nucleic Acids Res       Date:  1995-02-11       Impact factor: 16.971

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