CELLULAR UPTAKE OF OLIGONUCLEOTIDE ANALOGUES

寡核苷酸类似物的细胞摄取

基本信息

  • 批准号:
    3804715
  • 负责人:
  • 金额:
    --
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
  • 资助国家:
    美国
  • 起止时间:
  • 项目状态:
    未结题

项目摘要

Improving the cellular uptake of oligonucleotide analogues represents a critical issue with respect to the application of these biomolecules in the targeting of mRNAs or in the formation of triplex structures with genomic DNA as a means to control gene expression. Studies related to improve cellular uptake of oligonucleotide analogues have been scarce and poorly executed as far as refinement of the parameters is concerned. Our approach involves the systematic tailing of an oligonucleoside phosphorothioate of known biological activity against HIV, with monomeric polyethylene glycols at either the 3'-end, 5'-end or both ends and assay for the untailed phosphorothioate oligomer in chronically infected H9 cells. So far we have synthesized four different oligonucleoside phosphorothioates complementary to the mRNA encoded by the rev gene of HIV each of them covalently bound at both ends to 1, 2, 3, or 4 hexaethylene glycol monomer(s). These oligonucleotides have been purified to homogeneity on denaturing polyacrylamide gels and are ready for biological evaluation. All of these oligonucleotide analogues formed stable DNA duplexes with their complementary DNA sequences relative to the untailed oligonucleoside phosphorothioates. (The duplexes have the same Tm at 260 nm). It is to be noted, however, that the hexaethylene glycol monomers were linked together by phosphodiester bridges. To properly study the effect of added charges on the behavior of these biomolecules, oligonucleoside phosphorothioates will also be derivatized at the 3'-end with uncharged polyethylene glycol molecules of varying sizes (M.W. 1,000-8,000). Judith b. Regan has already purified a phosphorothioate oligomer conjugated to a relatively large polyethylene glycol monomer (M.W. 2,500). Tm experiments are currently being conducted., Dr. Mitsuya of the NCI will perform all the biological assays pertaining to these novel biomolecules.
提高细胞对寡核苷酸类似物的摄取代表了一个

项目成果

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S L BEAUCAGE其他文献

S L BEAUCAGE的其他文献

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{{ truncateString('S L BEAUCAGE', 18)}}的其他基金

ADVANCES IN THE SYNTHESIS OF OLIGONUCLEOTIDES VIA THE PHOSPHORAMIDITE APPROACH
通过亚磷酰胺方法合成寡核苷酸的进展
  • 批准号:
    3804713
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
AN IMPROVED SYNTHESIS OF OLIGODEOXYRIBONUCLEOSIDE PHOSPHOROTHIOATES
寡脱氧核糖核苷硫代磷酸酯的改进合成
  • 批准号:
    3792431
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
THE SYNTHESIS OF OLIGONUCLEOTIDES VIA THE PHOSPHORAMIDITE APPROACH
通过亚磷酰胺方法合成寡核苷酸
  • 批准号:
    3792433
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
ALTERNATING ALPHA,BETA-OLIGOTHYMIDYLATES AS MODEL ANTISENSE MOLECULES
交替α,β-寡核苷酸作为模型反义分子
  • 批准号:
    3792434
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
CHEMICAL SYNTHESIS OF OLIGONUCLEOTIDE ANALOGUES
寡核苷酸类似物的化学合成
  • 批准号:
    3748239
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
CHEMICAL SYNTHESIS OF OLIGONUCLEOTIDE ANALOGUES
寡核苷酸类似物的化学合成
  • 批准号:
    5200796
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
CHEMICAL SYNTHESIS OF OLIGONUCLEOTIDE ANALOGUES
寡核苷酸类似物的化学合成
  • 批准号:
    3748240
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
PEG-OLIGODEOXYRIBONUCLEOTIDE CONJUGATES
PEG-寡脱氧核糖核苷酸缀合物
  • 批准号:
    3770389
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
AN IMPROVED SYNTHESIS OF OLIGODEOXYRIBONUCLEOSIDE PHOSPHOROTHIOATES
寡脱氧核糖核苷硫代磷酸酯的改进合成
  • 批准号:
    3804710
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
CELLULAR UPTAKE OF OLIGONUCLEOTIDE ANALOGUES
寡核苷酸类似物的细胞摄取
  • 批准号:
    3792435
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:

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