Mimicry of molecular glues using dual covalent chimeras

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.

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Publication Details

Journal
Nature Communications
Published
2025-03-24
DOI
https://doi.org/10.1038/s41467-025-58083-z
Citations
4
Primary Topic
Click Chemistry and Applications
Type
article
Field-Weighted Citation Impact
3.74

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article

Mimicry of molecular glues using dual covalent chimeras

Nickolas Serniuck, Anthony F. Rullo, Eden Kapcan, Jonathan L. Bramson et al.
4 citations
Nature Communications
Click Chemistry and Applications
3.74
article

Mimicry of molecular glues using dual covalent chimeras

Nickolas Serniuck, Anthony F. Rullo, Eden Kapcan, Jonathan L. Bramson, Ali Zhang, Karolina Krygier, Maya da Luz
article en
4 citations

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.

Nature CommunicationsVol. 16(1)
McMaster University Medical Centre (CA), McMaster University (CA)
Canadian Network for Research and Innovation in Machining Technology, Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 8%
Click Chemistry and Applications
3.74
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