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Expanding the epitranscriptomic RNA sequencing and modification mapping mass spectrometry toolbox with field asymmetric waveform ion mobility and electrochemical elution liquid chromatography

Richard Lauman, Hee Jong Kim, Lindsay K. Pino, Alessandro Scacchetti, View ORCID ProfileRoberto Bonasio, Benjamin A. Garcia
doi: https://doi.org/10.1101/2022.10.28.514273
Richard Lauman
1Department of Biochemistry and Biophysics, University of Pennsylvania, Philadelphia, PA, USA
2Epigenetic Institute and Department of Cell and Developmental Biology, University of Pennsylvania, Philadelphia, PA, USA
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Hee Jong Kim
1Department of Biochemistry and Biophysics, University of Pennsylvania, Philadelphia, PA, USA
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Lindsay K. Pino
1Department of Biochemistry and Biophysics, University of Pennsylvania, Philadelphia, PA, USA
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Alessandro Scacchetti
2Epigenetic Institute and Department of Cell and Developmental Biology, University of Pennsylvania, Philadelphia, PA, USA
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Roberto Bonasio
2Epigenetic Institute and Department of Cell and Developmental Biology, University of Pennsylvania, Philadelphia, PA, USA
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  • ORCID record for Roberto Bonasio
Benjamin A. Garcia
3Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO, USA
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  • For correspondence: bagarcia@wustl.edu
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Abstract

Post-transcriptional modifications of RNA strongly influence RNA structure and function. Recent advances in RNA sequencing and mass spectrometry (MS) methods have identified over 140 of these modifications on a wide variety of RNA species. Most next-generation sequencing approaches can only map one RNA modification at a time, and while MS can assign multiple modifications simultaneously in an unbiased manner, MS cannot accurately catalog and assign RNA modifications in complex biological samples due to limitations in fragment length and coverage depth. Thus, a facile method to identify novel RNA modifications while simultaneously locating them in the context of their RNA sequences is still lacking. We combined two orthogonal modes of RNA ion separation before mass-spectrometry identification: high-field asymmetric ion mobility separation (FAIMS) and electrochemically modulated liquid chromatography (EMLC). FAIMS RNA-MS increases both coverage and throughput, while the EMLC LC-MS orthogonally separates RNA of different length and charge. The combination of the two methods offers a broadly applicable platform to improve length and depth of MS-based RNA sequencing while providing contextual access to the analysis of RNA modifications.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted October 30, 2022.
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Expanding the epitranscriptomic RNA sequencing and modification mapping mass spectrometry toolbox with field asymmetric waveform ion mobility and electrochemical elution liquid chromatography
Richard Lauman, Hee Jong Kim, Lindsay K. Pino, Alessandro Scacchetti, Roberto Bonasio, Benjamin A. Garcia
bioRxiv 2022.10.28.514273; doi: https://doi.org/10.1101/2022.10.28.514273
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Expanding the epitranscriptomic RNA sequencing and modification mapping mass spectrometry toolbox with field asymmetric waveform ion mobility and electrochemical elution liquid chromatography
Richard Lauman, Hee Jong Kim, Lindsay K. Pino, Alessandro Scacchetti, Roberto Bonasio, Benjamin A. Garcia
bioRxiv 2022.10.28.514273; doi: https://doi.org/10.1101/2022.10.28.514273

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