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Learning to Predict Mutation Effects of Protein-Protein Interactions by Microenvironment-aware Hierarchical Prompt Learning

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arxiv 2405.10348 v1 pith:6HKQXZSY submitted 2024-05-16 q-bio.QM cs.AIcs.LG

classification q-bio.QMcs.AIcs.LG
keywords mutationhierarchicalmicroenvironmentpromptcodebookdatalearningpre-training
verification ladder T0 review T1 audit T2 compute T3 formal
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Protein-protein bindings play a key role in a variety of fundamental biological processes, and thus predicting the effects of amino acid mutations on protein-protein binding is crucial. To tackle the scarcity of annotated mutation data, pre-training with massive unlabeled data has emerged as a promising solution. However, this process faces a series of challenges: (1) complex higher-order dependencies among multiple (more than paired) structural scales have not yet been fully captured; (2) it is rarely explored how mutations alter the local conformation of the surrounding microenvironment; (3) pre-training is costly, both in data size and computational burden. In this paper, we first construct a hierarchical prompt codebook to record common microenvironmental patterns at different structural scales independently. Then, we develop a novel codebook pre-training task, namely masked microenvironment modeling, to model the joint distribution of each mutation with their residue types, angular statistics, and local conformational changes in the microenvironment. With the constructed prompt codebook, we encode the microenvironment around each mutation into multiple hierarchical prompts and combine them to flexibly provide information to wild-type and mutated protein complexes about their microenvironmental differences. Such a hierarchical prompt learning framework has demonstrated superior performance and training efficiency over state-of-the-art pre-training-based methods in mutation effect prediction and a case study of optimizing human antibodies against SARS-CoV-2.

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Cited by 3 Pith papers

Reviewed papers in the Pith corpus that reference this work. Sorted by Pith novelty score. Full citation record

  1. Tokenizing Electron Cloud in Protein-Ligand Interaction Learning

    cs.LG 2025-05 conditional novelty 6.0 of 10

    ECBind tokenizes electron cloud densities via quantized embeddings and improves protein-ligand binding affinity prediction, especially per-structure correlations on MISATO.

  2. Predicting mutational effects on protein binding from folding energy

    q-bio.BM 2025-07 conditional novelty 5.0 of 10

    StaB-ddG predicts binding-affinity changes from folding-energy differences, matching FoldX accuracy on a homology-split SKEMPIv2.0 benchmark while running about 1,000 times faster.

  3. EnerBridge-DPO: Energy-Guided Protein Inverse Folding with Markov Bridges and Direct Preference Optimization

    cs.LG 2025-06 conditional novelty 5.0 of 10

    A Markov-bridge inverse folding model fine-tuned with energy-based preference pairs and an explicit ΔΔG loss designs lower-energy protein complex sequences while keeping sequence recovery close to state-of-the-art.

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