What are Thioaptamers?
Thioaptamers are extremely stable, nucleic acid-based molecules that can be designed with very high specificity and affinity to a wide range of important biomolecular targets.
Thioaptamers are unique and proprietary as a result of the chemical substitution of one or two sulfur atoms for the phosphoryl oxygens of an internucleoside phosphate.
Thioaptamer Characteristics
- Very high affinity for target proteins (picomolar to nanomolar: view presentation of data)
- Very high specificity
- Tremendous stability against nucleases
- Indefinite shelf-life – stable against denaturation (unlike antibodies)
- Inexpensive to produce synthetically
- Highly reproducible synthesis – excellent quality control
- Rapid discovery and production of new thioaptamers
- Potential therapeutics that avoid adverse immune reactions
- Backbone modifications and sequence are selected simultaneously
How Thioaptamers are Discovered
Selecting phosphorodithioate oligos (thioaptamers) can only be accomplished using AM's proprietary bead-based technology. Read a short paper on thioaptamers. The bead-based discovery process is a unique and novel technology that does not rely on rounds of enrichment of nucleic acids.