Author/Authors :
Michelle Sexton، نويسنده , , Grace Woodruff، نويسنده , , Eric A. Horne، نويسنده , , Yi-Hsing Lin، نويسنده , , Giulio G. Muccioli، نويسنده , , Mingfeng Bai، نويسنده , , Eric Stern، نويسنده , , Darryl J. Bornhop، نويسنده , , Nephi Stella، نويسنده ,
Abstract :
High-throughput screening (HTS) of chemical libraries is often used for the unbiased identification of compounds interacting with G protein-coupled receptors (GPCRs), the largest family of therapeutic targets. However, current HTS methods require removing GPCRs from their native environment, which modifies their pharmacodynamic properties and biases the screen toward false positive hits. Here, we developed and validated a molecular imaging (MI) agent, NIR-mbc94, which emits near infrared (NIR) light and selectively binds to endogenously expressed cannabinoid CB2 receptors, a recognized target for treating autoimmune diseases, chronic pain and cancer. The precision and ease of this assay allows for the HTS of compounds interacting with CB2 receptors expressed in their native environment.