Exploring zero-shot structure-based protein fitness prediction
- URL: http://arxiv.org/abs/2504.16886v1
- Date: Wed, 23 Apr 2025 17:01:09 GMT
- Title: Exploring zero-shot structure-based protein fitness prediction
- Authors: Arnav Sharma, Anthony Gitter,
- Abstract summary: We make zero-shot predictions about the fitness consequences of protein sequence changes with pre-trained machine learning models.<n>We assess several modeling choices for structure-based models and their effects on downstream fitness prediction.
- Score: 0.5524804393257919
- License: http://creativecommons.org/licenses/by/4.0/
- Abstract: The ability to make zero-shot predictions about the fitness consequences of protein sequence changes with pre-trained machine learning models enables many practical applications. Such models can be applied for downstream tasks like genetic variant interpretation and protein engineering without additional labeled data. The advent of capable protein structure prediction tools has led to the availability of orders of magnitude more precomputed predicted structures, giving rise to powerful structure-based fitness prediction models. Through our experiments, we assess several modeling choices for structure-based models and their effects on downstream fitness prediction. Zero-shot fitness prediction models can struggle to assess the fitness landscape within disordered regions of proteins, those that lack a fixed 3D structure. We confirm the importance of matching protein structures to fitness assays and find that predicted structures for disordered regions can be misleading and affect predictive performance. Lastly, we evaluate an additional structure-based model on the ProteinGym substitution benchmark and show that simple multi-modal ensembles are strong baselines.
Related papers
- CPE-Pro: A Structure-Sensitive Deep Learning Method for Protein Representation and Origin Evaluation [7.161099050722313]
We develop a structure-sensitive supervised deep learning model, Crystal vs Predicted Evaluator for Protein Structure (CPE-Pro)
CPE-Pro learns the structural information of proteins and captures inter-structural differences to achieve accurate traceability on four data classes.
We utilize Foldseek to encode protein structures into "structure-sequences" and trained a protein Structural Sequence Language Model, SSLM.
arXiv Detail & Related papers (2024-10-21T02:21:56Z) - ProteinBench: A Holistic Evaluation of Protein Foundation Models [53.59325047872512]
We introduce ProteinBench, a holistic evaluation framework for protein foundation models.
Our approach consists of three key components: (i) A taxonomic classification of tasks that broadly encompass the main challenges in the protein domain, based on the relationships between different protein modalities; (ii) A multi-metric evaluation approach that assesses performance across four key dimensions: quality, novelty, diversity, and robustness; and (iii) In-depth analyses from various user objectives, providing a holistic view of model performance.
arXiv Detail & Related papers (2024-09-10T06:52:33Z) - Structure-Informed Protein Language Model [38.019425619750265]
We introduce the integration of remote homology detection to distill structural information into protein language models.
We evaluate the impact of this structure-informed training on downstream protein function prediction tasks.
arXiv Detail & Related papers (2024-02-07T09:32:35Z) - xTrimoPGLM: Unified 100B-Scale Pre-trained Transformer for Deciphering the Language of Protein [74.64101864289572]
We propose a unified protein language model, xTrimoPGLM, to address protein understanding and generation tasks simultaneously.
xTrimoPGLM significantly outperforms other advanced baselines in 18 protein understanding benchmarks across four categories.
It can also generate de novo protein sequences following the principles of natural ones, and can perform programmable generation after supervised fine-tuning.
arXiv Detail & Related papers (2024-01-11T15:03:17Z) - Protein 3D Graph Structure Learning for Robust Structure-based Protein
Property Prediction [43.46012602267272]
Protein structure-based property prediction has emerged as a promising approach for various biological tasks.
Current practices, which simply employ accurately predicted structures during inference, suffer from notable degradation in prediction accuracy.
Our framework is model-agnostic and effective in improving the property prediction of both predicted structures and experimental structures.
arXiv Detail & Related papers (2023-10-14T08:43:42Z) - Multi-level Protein Representation Learning for Blind Mutational Effect
Prediction [5.207307163958806]
This paper introduces a novel pre-training framework that cascades sequential and geometric analyzers for protein structures.
It guides mutational directions toward desired traits by simulating natural selection on wild-type proteins.
We assess the proposed approach using a public database and two new databases for a variety of variant effect prediction tasks.
arXiv Detail & Related papers (2023-06-08T03:00:50Z) - CCPL: Cross-modal Contrastive Protein Learning [47.095862120116976]
We introduce a novel unsupervised protein structure representation pretraining method, cross-modal contrastive protein learning (CCPL)
CCPL leverages a robust protein language model and uses unsupervised contrastive alignment to enhance structure learning.
We evaluated our model across various benchmarks, demonstrating the framework's superiority.
arXiv Detail & Related papers (2023-03-19T08:19:10Z) - Structure-informed Language Models Are Protein Designers [69.70134899296912]
We present LM-Design, a generic approach to reprogramming sequence-based protein language models (pLMs)
We conduct a structural surgery on pLMs, where a lightweight structural adapter is implanted into pLMs and endows it with structural awareness.
Experiments show that our approach outperforms the state-of-the-art methods by a large margin.
arXiv Detail & Related papers (2023-02-03T10:49:52Z) - State-specific protein-ligand complex structure prediction with a
multi-scale deep generative model [68.28309982199902]
We present NeuralPLexer, a computational approach that can directly predict protein-ligand complex structures.
Our study suggests that a data-driven approach can capture the structural cooperativity between proteins and small molecules, showing promise in accelerating the design of enzymes, drug molecules, and beyond.
arXiv Detail & Related papers (2022-09-30T01:46:38Z) - Contrastive Representation Learning for 3D Protein Structures [13.581113136149469]
We introduce a new representation learning framework for 3D protein structures.
Our framework uses unsupervised contrastive learning to learn meaningful representations of protein structures.
We show, how these representations can be used to solve a large variety of tasks, such as protein function prediction, protein fold classification, structural similarity prediction, and protein-ligand binding affinity prediction.
arXiv Detail & Related papers (2022-05-31T10:33:06Z) - Structure-aware Protein Self-supervised Learning [50.04673179816619]
We propose a novel structure-aware protein self-supervised learning method to capture structural information of proteins.
In particular, a well-designed graph neural network (GNN) model is pretrained to preserve the protein structural information.
We identify the relation between the sequential information in the protein language model and the structural information in the specially designed GNN model via a novel pseudo bi-level optimization scheme.
arXiv Detail & Related papers (2022-04-06T02:18:41Z) - Transfer Learning for Protein Structure Classification at Low Resolution [124.5573289131546]
We show that it is possible to make accurate ($geq$80%) predictions of protein class and architecture from structures determined at low ($leq$3A) resolution.
We provide proof of concept for high-speed, low-cost protein structure classification at low resolution, and a basis for extension to prediction of function.
arXiv Detail & Related papers (2020-08-11T15:01:32Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.