Genetically Encoded, Biologically Responsive, And Programmable Bispecific Aptames As Therapeutic Protein Degraders

Tech ID: 34372 / UC Case 2026-067-0

Patent Status

Patent Pending

Brief Description

Engineered ribonucleic acid aptamers are designed with a modular architecture to target and bind specific proteins. Developed by researchers at UC Berkeley, these molecular tools include a domain A serving as a first target protein binding domain, a domain B functioning as a linker, and a domain C acting as a second target protein binding domain. In certain configurations, the aptamers can incorporate a domain D that undergoes a distinct conformational change when engaged by a specific ligand, enabling precise control over their activity.

Suggested uses

  • Development of targeted therapeutics that direct specific disease causing proteins to cellular degradation machinery

  • Genomic engineering applications utilizing donor deoxyribonucleic acid to integrate programmable regulatory sequences into safe harbor loci

  • High throughput screening assays to identify novel ribonucleic acid aptamers and functional protein binding domains

  • Creation of ligand responsive molecular switches for real time control of gene expression in synthetic biology frameworks

  • Diagnostic tools configured to detect and bind specific target proteins within complex biological samples

Advantages

  • Offers a highly modular and programmable architecture with multiple distinct domains for multifunctional protein targeting

  • Enables precise external control over molecular interactions through ligand induced conformational changes in specific domains

  • Provides enhanced molecular stability and diverse structural options through circularization and flanking ribozyme sequences

  • Allows for stable and predictable genomic integration by utilizing donor deoxyribonucleic acid targeted to safe harbor loci

  • Streamlines the discovery of new targeting tools via integrated methods for screening diverse aptamer sequences

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Inventors

  • Doudna, Jennifer A.

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