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Mimicry of molecular glues using dual covalent chimeras

Author

Listed:
  • Eden Kapcan

    (McMaster University
    McMaster University
    McMaster University)

  • Karolina Krygier

    (McMaster University
    McMaster University
    McMaster University)

  • Maya Luz

    (McMaster University)

  • Nickolas J. Serniuck

    (McMaster University
    McMaster University
    McMaster University)

  • Ali Zhang

    (McMaster University)

  • Jonathan Bramson

    (McMaster University
    McMaster University)

  • Anthony F. Rullo

    (McMaster University
    McMaster University
    McMaster University
    McMaster University)

Abstract

A special class of proximity inducing bifunctional molecules/chimeras called molecular glues leverage positive co-operativity to stabilize ternary complex formation and induce a biological response. Despite their utility, molecular glues remain challenging to rationally design. This is particularly true in the context of inducing cell-cell proximity which involve ternary complexes that comprise non- or negatively interacting proteins. In this work, we develop a dual proximity labeling strategy enabling a chimera to covalently crosslink a non-interacting serum antibody to a tumor surface protein, within a ternary complex. The resultant resistance to dissociation, including in the presence of competitor binding ligands, mimics molecular glue stabilization. We demonstrate these covalent glue mimics (CGMs) can induce cell-cell proximity in three distinct model systems of tumor-immune recognition, leading to significant functional enhancements. Collectively, this work underscores the utility of dual proximal covalent labeling as a potential general strategy to stabilize ternary complexes comprising non-interacting proteins and enforce cell-cell interactions.

Suggested Citation

  • Eden Kapcan & Karolina Krygier & Maya Luz & Nickolas J. Serniuck & Ali Zhang & Jonathan Bramson & Anthony F. Rullo, 2025. "Mimicry of molecular glues using dual covalent chimeras," Nature Communications, Nature, vol. 16(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-58083-z
    DOI: 10.1038/s41467-025-58083-z
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