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Quantitative Measurement of Cytosolic and Nuclear Penetration of Oligonucleotide Therapeutics
A major obstacle in the development of effective oligonucleotide therapeutics is a lack of understanding about their cytosolic and nuclear penetration. To address this problem, we have applied the chloroalkane penetration assay (CAPA) to oligonucleotide therapeutics. CAPA was used to quantitate cyto...
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Published in: | ACS chemical biology 2022-02, Vol.17 (2), p.348-360 |
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creator | Deprey, Kirsten Batistatou, Nefeli Debets, Marjoke F Godfrey, Jack VanderWall, Kirstin B Miles, Rebecca R Shehaj, Livia Guo, Jiaxing Andreucci, Amy Kandasamy, Pachamuthu Lu, Genliang Shimizu, Mamoru Vargeese, Chandra Kritzer, Joshua A |
description | A major obstacle in the development of effective oligonucleotide therapeutics is a lack of understanding about their cytosolic and nuclear penetration. To address this problem, we have applied the chloroalkane penetration assay (CAPA) to oligonucleotide therapeutics. CAPA was used to quantitate cytosolic delivery of antisense oligonucleotides (ASOs) and siRNAs and to explore the effects of a wide variety of commonly used chemical modifications and their patterning. We evaluated potential artifacts by exploring the effects of serum, comparing activity data and CAPA data, and assessing the impact of the chloroalkane tag and its linker chemistry. We also used viral transduction to expand CAPA to the nuclear compartment in epithelial and neuronal cell lines. Using this enhanced method, we measured a 48-h time course of nuclear penetration for a panel of chemically diverse modified RNAs. Moving forward, CAPA will be a useful tool for deconvoluting the complex processes of endosomal uptake, escape into the cytosol, and subcellular trafficking of oligonucleotide therapeutics in therapeutically relevant cell types. |
doi_str_mv | 10.1021/acschembio.1c00830 |
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To address this problem, we have applied the chloroalkane penetration assay (CAPA) to oligonucleotide therapeutics. CAPA was used to quantitate cytosolic delivery of antisense oligonucleotides (ASOs) and siRNAs and to explore the effects of a wide variety of commonly used chemical modifications and their patterning. We evaluated potential artifacts by exploring the effects of serum, comparing activity data and CAPA data, and assessing the impact of the chloroalkane tag and its linker chemistry. We also used viral transduction to expand CAPA to the nuclear compartment in epithelial and neuronal cell lines. Using this enhanced method, we measured a 48-h time course of nuclear penetration for a panel of chemically diverse modified RNAs. 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subjects | Cell Nucleus Cytosol - metabolism Oligonucleotides - metabolism Oligonucleotides, Antisense - metabolism RNA, Small Interfering - metabolism |
title | Quantitative Measurement of Cytosolic and Nuclear Penetration of Oligonucleotide Therapeutics |
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