Technologies that can be Used to Selectively Bind Messenger RNA and Enhance Protein Translation

Tech ID: 30486 / UC Case 2019-232-0

Background

Control of gene expression is a general approach to treat diseases where there is too much or too little of a gene product. However, while there are many methods which are available to downregulate the expression of messenger RNA transcripts, very few strategies can upregulate the endogenous gene product.

The vast majority of gene regulatory drugs which are commercially available or being developed are designed to knockdown gene expression (i.e. siRNAs, miRNAs, anti-sense, etc.). There exist some methods to enhance gene expression, such as the delivery of messenger RNAs; although, therapeutic delivery of such large and charged RNA molecules is technically challenging, inefficient, and may not be practical. There are also classical gene therapy approaches where a gene product is delivered as viral-encoded products (AAV or lentivirus-packaged).

However, these methods suffer from not being able to accurately reproduce the correct alternatively spliced isoforms in the right ratios in cells.

 

Technology Description

Researchers from UC San Diego have invented a means to leverage regulatory biology to enable the development of first-in-class gene targeting drugs that will selectively enhance protein translation. This technology encompasses two technologies that can be used to selectively bind messenger RNA and enhance protein translation. This technology can be targeted to any protein coding sequence encoded by the genome.

 

Applications

  • Reagent for Scientific Research. Reagents for controlled translation of a messenger RNA.
  • Drug/Therapeutic to treat disease. Therapeutic delivery for the treatment of diseases rooted in haploinsufficiency

Intellectual Property Info

UC San Diego is seeking companies interested in licensing this patent-pending technology to develop commercial products.

Patent Status

Patent Pending

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Other Information

Keywords

Protein translation, gene expression, mRNA

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