Adar-recruiting oligonucleotides

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Interfaculty Institute of Biochemistry, University of Tübingen, Tübingen, Germany Gene and RNA Therapy Center (GRTC), Faculty of Medicine, University of Tübingen, Tübingen, Germany (1)
Interfaculty Institute of Biochemistry, University of Tübingen, Tübingen, Germany Gene and RNA Therapy Center (GRTC), Faculty of Medicine, University of Tübingen, Tübingen, Germany iFIT Cluster of Excellence (EXC2180) "Image-Guided and Functionally Instructed Tumor Therapies, University of Tübingen, Tübingen, Germany (1)

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Stereo-random Oligonucleotides Enable Efficient Recruitment of ADAR in vitro and in vivo

We used our previously published isASO-ID protocol to identify binders for two different adenosine deaminases acting on RNA- (ADAR-) recruiting antisense oligonucleotides (ONs). The ONs differed in their phosphorothioate content and their RNA editing potency and efficiency through the recruitment of...

ORGANISM(S): Homo sapiens (Human)

2025-07-31 | PXD066763 | Pride

Inhibition of the RNA exosome by chemically stabilized long antisense oligonucleotides

The protein interactions of ADAR-recruiting oligonucleotides inside the cellular environment was identified using the isASO-ID protocol and SILAC-MS/MS. We identified two exoribonucleases to bind differently to the oligonucleotides with respect to their 3’-terminal 2’-ribose modifications leading to...

ORGANISM(S): Homo sapiens (Human)

2026-09-30 | PXD079777 | Pride

Antisense oligonucleotide Basu Proximity biotinylation Biotin ligase Silac Rna quality control In situ biotinylation Rna exosome

Programmable RNA editing with endogenous ADAR enzymes - a feasible option for the treatment of inherited retinal disease?

Not available

S-EPMC10244592 | biostudies-literature

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