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Updated: May 13, 2026

Oligopeptide Competition Assay for Phosphorylation Site Determination
Published on: May 18, 2017
Discovery of Phosphorylated Peptidomimetics Targeting Cbl-b SH2 Domain as Orthosteric Cbl-b Inhibitors by an
Erdong Li1, Xiuqi Hu1, Lvbin Hu1
1Jiang Su Key Laboratory of Drug Design and Optimization and Department of Medicinal Chemistry, School of Pharmacy, China Pharmaceutical University, Nanjing 210009, China.
None:
Casitas B-lineage lymphoma-b (Cbl-b), a pivotal negative regulator of TCR signaling, is highly expressed in immune cells. Its inhibition potentiates immune-mediated antitumor effects. Herein, we constructed a potent fluorescent tracer, Tracer 2, based on the Cbl-b peptide inhibitor Pep 1. Utilizing this tracer, we established a fluorescence polarization (FP) assay with enhanced sensitivity, discriminative capacity, and precision for the activity evaluation and high-throughput screening of orthosteric Cbl-b Src homology 2 (SH2) domain inhibitors. Leveraging this FP assay, we derived a potent phosphorylated peptidomimetic Cbl-b inhibitor, Pep 19, which significantly enhanced TCR signaling and promoted IL-2 secretion in Jurkat cells. Furthermore, in vivo studies demonstrated that Pep 19 exhibited robust immune-mediated antitumor effects in the CT26 syngeneic mouse model. This study not only established a validated FP-based screening platform but also identified Pep 19 as a lead compound for developing orthosteric Cbl-b SH2 domain small-molecule inhibitors for cancer immunotherapy.

