PROGRAMMABLE TYPE V RNA ENDONUCLEESE SYSTEMS

DE602022039540T2Active Publication Date: 2026-07-08BAYER AG
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Patent Information

Authority / Receiving Office
DE · DE
Patent Type
Patents
Current Assignee / Owner
BAYER AG
Filing Date
2022-06-09
Publication Date
2026-07-08

AI Technical Summary

Technical Problem

Existing CRISPR-Cas systems face challenges such as large size, limited activity in eukaryotic cells, off-target effects, immune response, complex RNA requirements, and size constraints for viral delivery, which hinder their use in gene therapy and other precise applications.

Method used

Development of novel Type V CRISPR Cas nucleases (B-GEn.1 and B-GEn.2) with optimized sgRNAs and reduced RNA synthesis burden, allowing for efficient targeting and editing in eukaryotic cells with improved specificity and reduced off-target activity.

Benefits of technology

The novel CRISPR Cas nucleases enable precise gene editing in eukaryotic cells with enhanced specificity and reduced RNA requirements, overcoming size constraints and off-target issues, making them suitable for therapeutic applications.

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