Docket #: S19-517
Three-Recombinase-Dependent Viral Expression for Increased Neuron Specificity
Stanford researchers have discovered a method (Triplesect) to express molecular payloads using three-recombinase-dependent viral expression. Triplesect restricts functional expression of molecular tools such as optogenetic tools, CRISPR or therapeutic genes to pre-defined cellular subpopulations. The targeting resolution of this method is achieved through a multiply-engineered approach utilizing Boolean logic to identify targeted neurons or other cells. For example, neurons expressing gene A AND gene B AND gene C, but no other combination are targeted. As a result, this additional recombinase allows researchers to have increased specificity in targeting restricted neuron subpopulations. Additionally, Triplesect's viral delivery mechanism saves 30x the cost per genetic payload when comparing a typical viral batch to a new transgenic mouse.
Stage of Research
Applications
- Targeting molecular tools
- Fluorescent proteins
- Genetically-encoded calcium indicators
- Optogenetic tools
- Synthetic and natural receptors
- Translational neuroscience research
Advantages
- Three levels of targeting resolution via Boolean operators
- Viral delivery is 30x cheaper per payload vs transgenic mouse models
Publications
Related Links
Patents
- Published Application: WO2021158651
- Published Application: 20230064644
Similar Technologies
-
Touchless Selection of Gene Modified Cell Therapies Through TRAC Intron Knockins S23-103Touchless Selection of Gene Modified Cell Therapies Through TRAC Intron Knockins
-
Super Recombinator (SuRe), a CRISPR/Cas9-based platform for the rapid incorporation of multiple transgenes at the same genetic locus S20-282Super Recombinator (SuRe), a CRISPR/Cas9-based platform for the rapid incorporation of multiple transgenes at the same genetic locus
-
CRISPR-based FOXP3 gene Engineered T cells and Hematopoietic Stem Cell Precursors to treat IPEX syndrome patients S21-023CRISPR-based FOXP3 gene Engineered T cells and Hematopoietic Stem Cell Precursors to treat IPEX syndrome patients