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arxiv:2607.22143

TriGlue: a Biology-Inspired Generative Model for Generating Molecular Glue-Induced Ternary Complex

Published on Aug 4
· Submitted by
Yuliang Yan
on Aug 6
Authors:
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Abstract

Molecular glue degraders have emerged as a promising strategy for targeted protein degradation by inducing ternary complex formation between an E3 ubiquitin ligase and a target protein. Despite their therapeutic potential, computational design of molecular glues remains largely unexplored. Unlike conventional structure-based drug design, molecular glue design is governed by the unknown protein-protein interface and requires the simultaneous modeling of ligand generation, protein-protein docking, and ternary complex assembly. In this work, we formulate molecular glue design as a ternary complex generation problem and propose a biology-inspired generative framework, TriGlue. Motivated by the mechanism of molecular glue action, we decompose ternary complex generation into two coupled stages: interface estimation and interface-conditioned complex generation. First, we develop an SE(3)-equivariant interface estimation module that predicts a geometrically constrained protein-protein interface from unbound monomer structures. Second, we introduce an interface-conditioned ternary flow matching network that jointly generates the molecular glue and predicts the rigid-body transformation required to assemble the ternary complex. Extensive experiments demonstrate that TriGlue generates chemically valid molecules and produces plausible ternary complexes, which highlight the potential of biology-inspired generative modeling for accelerating molecular glue discovery. Our code is available at https://github.com/yuliangyan0807/molecular-glue-design.

Community

Excited to share TriGlue, a biology-inspired generative framework for the de novo design of molecular glue-induced ternary complexes.

Unlike conventional structure-based drug design, molecular glue discovery involves an unknown protein–protein interface and requires ligand generation, protein docking, and ternary complex assembly to be modeled jointly. TriGlue addresses this challenge by decomposing the generation process into two coupled stages:

  1. An SE(3)-equivariant interface estimation module predicts a geometrically constrained protein–protein interface from unbound monomer structures.
  2. An interface-conditioned ternary flow matching network jointly generates the molecular glue and predicts the rigid-body transformation required to assemble the ternary complex.

triglue

Experiments on TernaryDB show that TriGlue generates chemically valid molecules and structurally plausible ternary complexes. It also improves overall docking acceptance compared with DeepTernary and substantially outperforms existing interface-prediction baselines.

We hope this work provides a new direction for AI-driven targeted protein degradation by moving beyond ternary structure prediction toward the de novo generation of molecular glues and ternary complexes. We welcome feedback from the community!

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