| Literature DB >> 35213018 |
Remko Goossens1, Annemieke Aartsma-Rus2.
Abstract
Antisense oligonucleotides (AONs) are small synthetic molecules of therapeutic interest for a variety of human disease. Their ability to bind mRNA and affect its splicing gives AONs potential use for exon skipping therapies aimed at restoring the dystrophin transcript reading frame for Duchenne muscular dystrophy (DMD) patients. The neutrally charged phosphorodiamidate morpholino oligomers (PMOs) are a stable and relatively nontoxic AON modification. To assess exon skipping efficiency in vitro, it is important to deliver them to target cells. Here, we describe a method for the delivery of PMOs to myoblasts by electroporation. The described protocol for the Amaxa 4D X unit nucleofector system allows efficient processing of 16 samples in one nucleocuvette strip, aiding in high-throughput PMO efficacy screens.Entities:
Keywords: AON; DMD; Duchenne muscular dystrophy; Electroporation; Myocytes; Nucleofection; PMO
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Year: 2022 PMID: 35213018 DOI: 10.1007/978-1-0716-2010-6_12
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745