Abstrakt
Identifying protein targets of bioactive small molecules often requires complex, lengthy development of affinity probes. We present a method for stochastic modification of small molecules of interest with a photo-activatable phenyldiazirine linker.
The resulting isomeric mixture is conjugated to a hydrophilic copolymer decorated with biotin and a fluorophore. We validated this approach using known inhibitors of several medicinally relevant enzymes.
At least a portion of the stochastic derivatives retained their binding to the target, enabling target visualization, isolation, and identification. Moreover, the mix of stochastic probes could be separated into fractions and tested for binding affinity.
The structure of the active probe could be determined and the probe resynthesized to improve binding efficiency. Our approach an thus enable rapid target isolation, identification, and visualization, while providing information required for subsequent synthesis of an optimized probe.