Sequencing of Phosphorodiamidate Morpholino Oligomers by Hydrophilic Interaction Chromatography Coupled to Tandem Mass Spectrometry

Sequencing of phosphorodiamidate morpholino oligomers (PMOs) by hydrophilic interaction chromatography (HILIC) coupled to tandem mass spectrometry (MS/MS) is reported. The MS/MS analysis was performed using a quadrupole/time-of-flight (Q-ToF) mass analyzer and collision induced dissociation (CID) in negative ion mode. To improve MS sensitivity in negative ion mode, HILIC conditions, including the separation column, mobile phases, and MS parameters, were optimized. Using the developed HILIC-CID-MS/MS method, 100% sequence coverage was achieved for PMOs ranging from 18-mer to 25-mer. Additionally, the method was successfully applied to identifying positional isomers of <i>n</i> - 1 deletion impurities present in PMO drug substances.

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Publication Details

Journal
Journal of the American Society for Mass Spectrometry
Published
2024-08-30
DOI
https://doi.org/10.1021/jasms.4c00281
Citations
5
Primary Topic
Analytical Chemistry and Chromatography
Type
article
Field-Weighted Citation Impact
1.20
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article

Sequencing of Phosphorodiamidate Morpholino Oligomers by Hydrophilic Interaction Chromatography Coupled to Tandem Mass Spectrometry

Mingming Wang, Tao Wei, Brian O’Day, Brian Michaels et al.
5 citations
Journal of the American Society for Mass Spectrometry
Analytical Chemistry and Chromatography
1.20
article

Sequencing of Phosphorodiamidate Morpholino Oligomers by Hydrophilic Interaction Chromatography Coupled to Tandem Mass Spectrometry

Mingming Wang, Tao Wei, Brian O’Day, Brian Michaels, Jurjus Jurayj, Bao Zhong Cai
article en
5 citations

Abstract

Sequencing of phosphorodiamidate morpholino oligomers (PMOs) by hydrophilic interaction chromatography (HILIC) coupled to tandem mass spectrometry (MS/MS) is reported. The MS/MS analysis was performed using a quadrupole/time-of-flight (Q-ToF) mass analyzer and collision induced dissociation (CID) in negative ion mode. To improve MS sensitivity in negative ion mode, HILIC conditions, including the separation column, mobile phases, and MS parameters, were optimized. Using the developed HILIC-CID-MS/MS method, 100% sequence coverage was achieved for PMOs ranging from 18-mer to 25-mer. Additionally, the method was successfully applied to identifying positional isomers of <i>n</i> - 1 deletion impurities present in PMO drug substances.

Journal of the American Society for Mass SpectrometryVol. 35(10)
Sarepta Therapeutics (United States) (US)
Openalex Percentile: Top 24%
Analytical Chemistry and Chromatography
1.20
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