ALyzer3D.AI: a more generalizable deep learning predictor of light chain amyloidogenicity powered by structural and evolutionary Artificial Intelligence.

IF 5.1 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Peter May, Johannes Jung, Marion Högner, Florian Bassermann
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引用次数: 0

Abstract

Background: Predicting amyloidogenic risk of immunoglobulin light chains in amyloid light-chain (AL) amyloidosis is a major challenge, and existing computational models fail to generalize to new patient data.

Methods: We developed ALyzer3D.AI, a multi-modal deep learning architecture that integrates evolutionary features from the ESM-2 Protein Language Model, structural metrics from ColabFold and engineered biophysical features. Generalizability was evaluated on published and independent datasets, and model interpretability was assessed using IMGT-aligned SHapley Additive exPlanations (SHAP).

Results: While existing models dropped in performance on new data (accuracy 0.42-0.56), ALyzer3D.AI maintained an accuracy of 0.65 when trained and tested on the same datasets. A final model built on the full combined cohort of 5261 sequences achieved stable performance across repeated splits, with independent test AUC of 0.86 and accuracy of 0.84 at an optimized decision threshold. Performance arose from synergistic integration of PLM, structural and scalar features. PLM attributions were broadly distributed and slightly enriched in framework regions, whereas structural SHAP values were concentrated in CDRs and FR4. The most informative positions had intermediate sequence entropy.

Conclusions: ALyzer3D.AI provides a robust, interpretable tool for predicting light-chain amyloidogenicity that generalizes better to independent datasets than existing methods. It is publicly available via https://colab.research.google.com/github/pcmay/ALyzer3D.AI/blob/main/ALyzer3DAI.ipynb.

ALyzer3D。人工智能:由结构和进化人工智能驱动的更通用的轻链淀粉样变性深度学习预测器。
背景:预测淀粉样蛋白轻链(AL)淀粉样变性中免疫球蛋白轻链的淀粉样变性风险是一个主要挑战,现有的计算模型无法推广到新的患者数据。方法:开发ALyzer3D。AI是一种多模态深度学习架构,集成了ESM-2蛋白质语言模型的进化特征、ColabFold的结构指标和工程生物物理特征。在已发表的和独立的数据集上评估了通用性,并使用与imgt对齐的SHapley加性解释(SHAP)评估了模型的可解释性。结果:虽然现有模型在新数据上的性能下降(精度0.42-0.56),但ALyzer3D。在相同的数据集上进行训练和测试时,人工智能的准确率保持在0.65。基于5261个序列的完整组合队列构建的最终模型在重复分割中表现稳定,在优化决策阈值下,独立测试AUC为0.86,准确率为0.84。性能源于PLM、结构和标量特征的协同集成。PLM属性在框架区分布广泛且略富集,而结构SHAP值则集中在cdr和FR4。信息量最大的位置具有中间序列熵。结论:ALyzer3D。人工智能为预测轻链淀粉样变性提供了一个强大的、可解释的工具,与现有方法相比,它可以更好地推广到独立的数据集。它可以通过https://colab.research.google.com/github/pcmay/ALyzer3D.AI/blob/main/ALyzer3DAI.ipynb公开获取。
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来源期刊
Amyloid-Journal of Protein Folding Disorders
Amyloid-Journal of Protein Folding Disorders 生物-生化与分子生物学
CiteScore
10.60
自引率
10.90%
发文量
48
审稿时长
6-12 weeks
期刊介绍: Amyloid: the Journal of Protein Folding Disorders is dedicated to the study of all aspects of the protein groups and associated disorders that are classified as the amyloidoses as well as other disorders associated with abnormal protein folding. The journals major focus points are: etiology, pathogenesis, histopathology, chemical structure, nature of fibrillogenesis; whilst also publishing papers on the basic and chemical genetic aspects of many of these disorders. Amyloid is recognised as one of the leading publications on amyloid protein classifications and the associated disorders, as well as clinical studies on all aspects of amyloid related neurodegenerative diseases and major clinical studies on inherited amyloidosis, especially those related to transthyretin. The Journal also publishes book reviews, meeting reports, editorials, thesis abstracts, review articles and symposia in the various areas listed above.
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