Pith. sign in

REVIEW 2 cited by

Progressive Multi-Modality Learning for Inverse Protein Folding

Not yet reviewed by Pith; the record is open.

This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.

SPECIMEN: schema-true, not a live event

T0 review · schema-true

One-sentence machine reading of the paper's core claim.

pith:XXXXXXXX · record.json · timestamp

arxiv 2312.06297 v2 pith:SFMG5TGE submitted 2023-12-11 cs.AI

classification cs.AI
keywords proteinlearningmmdesigndatadesignfoldingfurtherinverse
verification ladder T0 review T1 audit T2 compute T3 formal
0 comments
read the original abstract

While deep generative models show promise for learning inverse protein folding directly from data, the lack of publicly available structure-sequence pairings limits their generalization. Previous improvements and data augmentation efforts to overcome this bottleneck have been insufficient. To further address this challenge, we propose a novel protein design paradigm called MMDesign, which leverages multi-modality transfer learning. To our knowledge, MMDesign is the first framework that combines a pretrained structural module with a pretrained contextual module, using an auto-encoder (AE) based language model to incorporate prior protein semantic knowledge. Experimental results, only training with the small dataset, demonstrate that MMDesign consistently outperforms baselines on various public benchmarks. To further assess the biological plausibility, we present systematic quantitative analysis techniques that provide interpretability and reveal more about the laws of protein design.

Discussion (0). Continue with ORCID to comment.

Forward citations

Cited by 2 Pith papers

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

  1. DapPep: Domain Adaptive Peptide-agnostic Learning for Universal T-cell Receptor-antigen Binding Affinity Prediction

    q-bio.QM 2024-11 conditional novelty 5.0 of 10

    DapPep, built from ESM-2 with cross-attention and peptide-reconstruction pre-training, reports ROC-AUC 0.816 and PR-AUC 0.836 on unseen peptides, beating PanPep by about 9 to 11 percent.

  2. Pan-protein Design Learning Enables Task-adaptive Generalization for Low-resource Enzyme Design

    q-bio.QM 2024-11 conditional novelty 5.0 of 10

    CrossDesign aligns pretrained protein language models with structure encoders to improve enzyme sequence design and zero-shot mutation fitness prediction.

Pith tools