RNA Characterization and Monitoring Solutions

RNA Characterization and Monitoring Solutions

Higher quality data and robust digestion, faster.

Higher quality data and robust digestion, faster.

RNA scientists using LC-MS need faster, higher-quality data due to the complex structures, modifications, and variants of RNA molecules. Typically, RNA is digested with an endonuclease before injection, and the fragments are separated using ion pairing reversed phase (IPRP) or hydrophilic chromatography (HILIC) coupled with mass spectrometry for detailed characterization. RNase plays a crucial role in studying RNA sequences, modifications, and impurities, ensuring the safety and efficacy of new therapeutics and vaccines. Advanced informatic tools enhance data acquisition, processing, and reporting, making them essential for method development and quality control labs. Waters RNA Characterization Tools offer robust digestion, improved MS spectra quality, and advanced data interpretation and reporting.


Webinar: Cracking the Code

LC-MS Fragment Mapping with Enhanced Sample Preparation and Informatics Tools

LC-MS Fragment Mapping with Enhanced Sample Preparation and Informatics Tools

To analyze larger therapeutic RNAs, they must be broken down into smaller fragments. Novel RNA endonucleases, high-purity mobile phase reagents, and integrated data processing workflows now simplify and automate these tasks, making LC-MS assays more accessible. These innovations lower the adoption barrier for LC-MS, accelerating the development and market readiness of RNA-based therapeutics.

This webinar will feature insights from Quality Assistance, highlighting their implementation of Waters' latest RNA solutions and discussing the analytical benefits these new tools have provided


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waters_connect App for RNA Fragment Mapping and Sequencing

The waters_connect MAP Sequence App automates and streamlines digested RNA fragment LC-MS mapping, and LC-MSE fragmentation-based sequencing from experiment planning through data acquisition, data processing, results review and reporting.

  • Simple, streamlined informatics workflows for digested RNA fragment mapping (LC-MS), and fragmentation-based RNA sequencing (LC-MSE) analysis
  • Enables the combination of data from the analysis of multiple digested samples for confident and complete sequence coverage
  • Complements the use of the waters_connect INTACT Mass App for targeted mRNA 5‘ Capping efficiency and 3‘ PolyA Tail heterogeneity analyses
  • Compliance-ready waters_connect informatics platform for deployment in regulated laboratories and labs where data integrity is important
  • Fully compatible with Waters RapiZyme RNases, other commercially available RNases, and customized enzymes for ultimate method flexibility


RapiZyme RNases: A Cut Above

RapiZyme RNases are novel endonucleases designed to produce unique fragments with lengths optimal for LC-MS identification, thereby improving sequence coverage and modification mapping.

  • Achieve sequence coverage with an easy to implement procedure
  • Generate unique digestion products for increased coverage
  • Tune your digestion protocol with high reproducibility
  • Integrated within MAP Sequence for streamlined interpretation
  • No need for chemical denaturants or inhibitors


Ionhance: Enhance your MS Data

Waters IonHance HFIP is stringently purified to obtain the lowest metals content necessary for the cleanest MS spectra.

  • High purity HFIP reagent for LC-MS analysis
  • Annotate your MS data with clarity
  • 2x lower sodium and potassium adducts
  • Have confidence in your supply with Waters quality manufacturing
  • Enhance your IP-RP and HILIC LC-MS methods


High Quality Nucleic Acid Standards

Choose the reference material that most closely matches your molecule with individual and pre-mixed nucleic acid sequences for LC-MS analysis.

  • Optimize IP-RP And HILIC methods with sgRNA LC-MS (1 nmol) reference standard
  • High purity reference material for development and system suitability
  • Increased confidence in method and system benchmarking
  • 100 nt sequence with modified termini (e.g. PS, 2’-OMe)
  • Perform intact or fragment analysis with a known sequence

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