Chemo-Click: Receptor-Controlled and Bioorthogonal Chemokine Ligation for Real-time Imaging of Drug-Resistant Leukemic B Cells

Research output: Contribution to journalArticlepeer-review

Abstract

Drug resistance in B cell leukemia is characterized by the co-expression of CXCR5 and CXCR3 chemokine receptors, making it a valuable biomarker for patient stratification. Herein we report a novel platform of activatable chemokines to selectively image drug-resistant leukemic B cells for the first time. The C-terminal derivatization of the human chemokines CXCL13 and CXCL10 with bioorthogonal tetrazine-BODIPY and BCN groups retained binding and internalization via their cognate CXCR5 and CXCR3 receptors and enabled rapid fluorescence labeling of CXCR5+ CXCR3+ resistant B cells -but not drug-susceptible leukemic cells- via intracellular chemokine ligation. This modular chemical approach offers a versatile strategy for real-time immunophenotyping of cell populations with distinct chemokine profiles and will accelerate the design of new precision medicine tools to advance personalized therapies in blood tumors.
Original languageEnglish
Pages (from-to)30565-30572
JournalJournal of the American Chemical Society
Volume146
Issue number44
DOIs
Publication statusPublished - 6 Nov 2024

Keywords / Materials (for Non-textual outputs)

  • Boron Compounds/chemistry
  • Humans
  • Cell Line, Tumor
  • Drug Resistance, Neoplasm
  • Leukemia, B-Cell/drug therapy
  • Chemokines/metabolism
  • Molecular Structure

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