Induced proximity-based therapeutic modalities
Summary
Proximity is a key component of nearly all regulatory pathways within biological systems. Over the past few decades, the rapid development of induced proximity modalities has allowed for therapeutic intervention beyond classical occupancy-driven pharmacology. These modalities comprise multispecific small molecules or biologic agents that co-opt native biological pathways by inducing an interaction between biomolecules. Small-molecule 'molecular glues' modify protein surfaces to induce non-
Content
# Induced proximity-based therapeutic modalities
*Published: 2026 Mar*
Proximity is a key component of nearly all regulatory pathways within biological
systems. Over the past few decades, the rapid development of induced proximity
modalities has allowed for therapeutic intervention beyond classical
occupancy-driven pharmacology. These modalities comprise multispecific small
molecules or biologic agents that co-opt native biological pathways by inducing
an interaction between biomolecules. Small-molecule 'molecular glues' modify
protein surfaces to induce non-native interactions or to stabilize existing
protein-protein interactions. They have been in the clinic since the 1980s but
have more recently been shown to enable targeted protein degradation or
inhibition and have been rationally designed to achieve this. Early discoveries
on molecular glues spearheaded the development of next-generation
heterobifunctional modalities for targeted protein degradation, such as
proteolysis-targeting chimeras, which are seeing early-stage clinical success.
Here, we aim to survey the field of induced proximity with a focus on potential
therapeutic applications. We discuss the emergence of novel approaches to
control cellular processes beyond protein degradation, including
post-translational modifications, cellular localization and transcriptional
activation. Some of these approaches are showing preclinical efficacy in various
disease models.
DOI: 10.1038/s41573-025-01316-z