LGQMOct 17, 2024

DPLM-2: A Multimodal Diffusion Protein Language Model

arXiv:2410.13782v172 citationsh-index: 7ICLR
Originality Incremental advance
AI Analysis

This addresses the challenge of joint sequence-structure generation in computational biology, offering a more integrated solution for protein design, though it builds incrementally on prior diffusion models.

The paper tackles the problem of generative protein modeling by introducing DPLM-2, a multimodal diffusion protein language model that simultaneously generates amino acid sequences and 3D structures, eliminating the need for a two-stage approach and showing competitive performance in tasks like folding and inverse folding.

Proteins are essential macromolecules defined by their amino acid sequences, which determine their three-dimensional structures and, consequently, their functions in all living organisms. Therefore, generative protein modeling necessitates a multimodal approach to simultaneously model, understand, and generate both sequences and structures. However, existing methods typically use separate models for each modality, limiting their ability to capture the intricate relationships between sequence and structure. This results in suboptimal performance in tasks that requires joint understanding and generation of both modalities. In this paper, we introduce DPLM-2, a multimodal protein foundation model that extends discrete diffusion protein language model (DPLM) to accommodate both sequences and structures. To enable structural learning with the language model, 3D coordinates are converted to discrete tokens using a lookup-free quantization-based tokenizer. By training on both experimental and high-quality synthetic structures, DPLM-2 learns the joint distribution of sequence and structure, as well as their marginals and conditionals. We also implement an efficient warm-up strategy to exploit the connection between large-scale evolutionary data and structural inductive biases from pre-trained sequence-based protein language models. Empirical evaluation shows that DPLM-2 can simultaneously generate highly compatible amino acid sequences and their corresponding 3D structures eliminating the need for a two-stage generation approach. Moreover, DPLM-2 demonstrates competitive performance in various conditional generation tasks, including folding, inverse folding, and scaffolding with multimodal motif inputs, as well as providing structure-aware representations for predictive tasks.

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