Bicycle Therapeutics Announces Publication of Article in Bioconjugate Chemistry, Describing an Extension of its Proprietary Technology Platform Based on Bicyclic Peptides
The article, titled Gold-Mediated Multiple Cysteine Arylation for the Construction of Highly Constrained Bicycle Peptides is available at the publications section of the Bicycle website at this link .
- The article, titled Gold-Mediated Multiple Cysteine Arylation for the Construction of Highly Constrained Bicycle Peptides is available at the publications section of the Bicycle website at this link .
- Assessment of the suitability of this methodology to Bicycle phage screening is underway, said Kevin Lee, Ph.D., Chief Executive Officer of Bicycle Therapeutics.
- Bicycles are formed through the reaction of three cysteine residues within a linear sequence with a trivalent, symmetrical small molecule scaffold.
- Bicycles with high binding affinities to therapeutically important targets are discovered using a proprietary phage display technology.