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Charge-State-Dependent Collision-Induced Dissociation Behaviors of RNA Oligonucleotides via High-Resolution Mass
Rui-Xiang Sun1,2, Mei-Qing Zuo1,2, Ji-Shuai Zhang1,2
1National Institute of Biological Sciences, Beijing 102206, China.
Abstract:
Mass spectrometry (MS)-based analysis of RNA oligonucleotides (oligos) plays an increasingly important role in the development of RNA therapeutics and epitranscriptomics research. However, MS fragmentation behaviors of RNA oligomers are understood insufficiently. Herein, we characterized the negative-ion-mode fragmentation behaviors of 26 synthetic RNA oligos containing four to eight nucleotides using collision-induced dissociation (CID) on a high-resolution, accurate-mass instrument. We found that in CID spectra acquired under the normalized collision energy (NCE) of 35%, approximately 70% of the total peak intensity was attributed to sequencing ions (a-B, a, b, c, d, w, x, y, z), around 25% of the peak intensity came from precursor ions that experienced complete or partial loss of a nucleobase in the form of either a neutral or an anion, and the remainder were internal ions and anionic nucleobases. The top five sequencing ions were the y, c, w, a-B, and a ions. Furthermore, we observed that CID fragmentation behaviors of RNA oligos were significantly impacted by their precursor charge. Specifically, when the precursors had a charge from 1- to 5-, the fractional intensity of sequencing ions decreased, while that of precursors that underwent either neutral or charged losses of a nucleobase increased. Additionally, we found that RNA oligos containing 3'-U tended to produce precursors with HNCO and/or NCO- losses, which presumably corresponded to isocyanic acid and cyanate anion, respectively. These findings provide valuable insights for better comprehending the mechanism behind RNA fragmentation by MS/MS, thereby facilitating the future automated identification of RNA oligos based on their CID spectra in a more efficient manner.
Insights
Mass spectrometry fragmentation of RNA oligonucleotides is better understood. Key sequencing ions and nucleobase loss patterns were identified, aiding automated RNA analysis.
Area of Science:
- Analytical Chemistry
- Biochemistry
- Molecular Biology
Background:
- Mass spectrometry (MS) is crucial for RNA therapeutics and epitranscriptomics.
- Understanding RNA oligonucleotide fragmentation in MS is limited.
Purpose of the Study:
- Characterize negative-ion mode fragmentation of RNA oligonucleotides using collision-induced dissociation (CID).
- Identify major fragmentation pathways and influential factors like precursor charge.
Main Methods:
- Analyzed 26 synthetic RNA oligonucleotides (4-8 nucleotides) using high-resolution MS.
- Utilized collision-induced dissociation (CID) at normalized collision energy (NCE) of 35%.
Main Results:
- Sequencing ions comprised ~70% of peak intensity, with y, c, w, a-B, and a ions being most abundant.
- Precursor charge significantly impacted fragmentation; higher charges reduced sequencing ions and increased nucleobase loss.
- 3'-U containing oligos showed specific HNCO and/or NCO- losses.
Conclusions:
- Detailed fragmentation behavior of RNA oligos under CID provides insights into MS/MS mechanisms.
- Findings facilitate more efficient automated identification of RNA oligonucleotides from MS/MS spectra.
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