Proteoform-level drug target landscapes demonstrates a wider spectrum of ibrutinib targets
Ontology highlight
ABSTRACT: In this study, we investigated the target landscape of the drug ibrutinib using thermal proteome profiling (TPP) and proteoform detection. Our findings demonstrated that ibrutinib interacts with multiple proteoforms, beyond its known targets. Specifically, we identified interactions related to immunomodulation, Golgi trafficking, endosomal trafficking, and glycosylation. These insights shed light on the clinical off-target effects and adverse events associated with ibrutinib. Moreover, our study emphasizes the significance of studyin drug interactions at the proteoform level and its potential implications for precision medicine.
INSTRUMENT(S): Q Exactive HF
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): B Cell, Cell Suspension Culture, Type I Cell Of Adrenal Cortex
DISEASE(S): Acute Leukemia
SUBMITTER: Rozbeh Jafari
LAB HEAD: Rozbeh Jafari
PROVIDER: PXD047187 | Pride | 2024-11-24
REPOSITORIES: Pride
ACCESS DATA