Middle-out sequence confirmation of CRISPR/Cas9 single guide RNA (sgRNA) using DNA primers and ribonuclease T1 digestion

Accurate sequencing of single guide RNAs (sgRNAs) for CRISPR/Cas9 genome editing is critical for patient safety, as the sgRNA guides the Cas9 nuclease to target site-specific cleavages in DNA. An approach to fully sequence sgRNA using protective DNA primers followed by ribonuclease (RNase) T1 digestion was developed to facilitate the analysis of these larger molecules by hydrophilic interaction liquid chromatography coupled with high-resolution mass spectrometry (HILIC-HRMS). Without RNase digestion, top-down mass spectrometry alone struggles to properly fragment precursor ions in large RNA oligonucleotides to provide confidence in sequence coverage. With RNase T1 digestion of these larger oligonucleotides, however, bottom-up analysis cannot confirm full sequence coverage due to the presence of short, redundant digestion products. By combining primer protection with RNase T1 digestion, digestion products are large enough to prevent redundancy and small enough to provide base resolution by tandem mass spectrometry to allow for full sgRNA sequence coverage. An investigation into the general requirements for adequate primer protection of specific regions of the RNA was conducted, followed by the development of a generic protection and digestion strategy that may be applied to different sgRNA sequences. This middle-out technique has the potential to expedite accurate sequence confirmation of chemically modified sgRNA oligonucleotides.

Automated summary

Accurate sequencing of sgRNAs is crucial for CRISPR/Cas9 genome editing, and a method using protective DNA primers and RNase T1 digestion coupled with HILIC-HRMS was developed. Without RNase digestion, top-down mass spectrometry struggles to fragment precursor ions in large RNA oligonucleotides. However, combining primer protection with RNase T1 digestion allows for full sgRNA sequence coverage by providing large enough digestion products to prevent redundancy and small enough products for base resolution by tandem mass spectrometry. This technique has the potential to expedite accurate sequence confirmation of chemically modified sgRNA oligonucleotides.