Ask any question about EPFL courses, lectures, exercises, research, news, etc. or try the example questions below.
DISCLAIMER: The Graph Chatbot is not programmed to provide explicit or categorical answers to your questions. Rather, it transforms your questions into API requests that are distributed across the various IT services officially administered by EPFL. Its purpose is solely to collect and recommend relevant references to content that you can explore to help you answer your questions.
Allosteric inhibitors represent a promising avenue for developing highly selective therapeutic drugs and overcoming drug resistance in kinase-targeted therapies. However, conventional screening methods are often limited by their reliance on known binding sites or by their low throughput. Here, we present a label-free nanopore tweezer approach that specifically detects allosteric binders to Abl kinase by monitoring ligand-induced ionic current fluctuations. In this method, an Abl kinase with a blocked active site is trapped within a cytolysin A (ClyA) nanopore, allowing real-time, single-molecule observation of co-binding of ATP-competitive and allosteric inhibitors to the Abl molecule. This strategy requires no prior structural knowledge of allosteric sites and is adaptable to high-throughput screening across the kinome and other enzyme targets. Our findings establish nanopore tweezers as a structure-based platform for identifying both allosteric modulators and co-drug combinations for a single target, thereby potentially accelerating the discovery of highly selective therapeutic agents.