Evaluation of siRNA stability and interaction with serum components using an agarose gel-based single-molecule FRET labeling method

Martina Tuttolomondo*, Henrik J. Ditzel

*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

Abstract

Small interfering RNAs (siRNAs) are RNA molecules with promising therapeutic potential as a result of their selective mRNA cleavage. However, despite recent progress, low stability in the bloodstream is an impediment to successful administration in vivo. Thus, the availability of flexible and rapid methods for studying siRNA stability and vehicles is crucial for future novel siRNA-based therapeutics. Herein, we report a fast Förster resonance energy transfer (FRET) method based on agarose gel electrophoresis to evaluate the stability of siRNA in serum as well as siRNA interaction with serum proteins and enzymes.

Original languageEnglish
Title of host publicationDesign and Delivery of SiRNA Therapeutics
EditorsHenrik J. Ditzel, Martina Tuttolomondo, Sakari Kauppinen
Volume2282
PublisherHumana Press
Publication date2021
Pages43-56
ISBN (Print) 978-1-0716-1297-2
ISBN (Electronic)978-1-0716-1298-9
DOIs
Publication statusPublished - 2021
SeriesMethods in Molecular Biology
Volume2282
ISSN1064-3745

Bibliographical note

Publisher Copyright:
© Springer Science+Business Media, LLC, part of Springer Nature 2021.

Keywords

  • Agarose gel electrophoresis
  • Förster resonance energy transfer
  • RNA interference
  • Serum protein corona
  • siRNA stability
  • Small interfering RNA

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