4.7 Article

PRESTO: Rapid protein mechanical strength prediction with an end-to-end deep learning model

期刊

EXTREME MECHANICS LETTERS
卷 55, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.eml.2022.101803

关键词

Deep learning; Protein; Protein mechanical strength; Biomaterials; Pulling force

资金

  1. MIT -IBM AI lab and MIT Quest, ONR [N000141612333, N000141912375]
  2. AFOSR, United States of America [FATE MURI FA9550-15-1-0514]
  3. NIH, United States of America [U01 EB014976]
  4. ARO, United States of America [W911NF1920098]
  5. Leonard S. Schleifer of Regeneron Pharmaceuticals, Inc.
  6. Center for Excellence in Education
  7. MIT

向作者/读者索取更多资源

The article introduces a deep learning model called PRESTO, which can rapidly and accurately predict the mechanical strength of proteins, successfully identifying mutation locations that may influence protein strength. The model can be used to design new protein sequences and establishes a unique protein strength curve.
Proteins often form biomaterials with exceptional mechanical properties equal or even superior to synthetic materials. Currently, using experimental atomic force microscopy or computational molecular dynamics to evaluate protein mechanical strength remains costly and time-consuming, limiting large-scale de novo protein investigations. Therefore, there exists a growing demand for fast and accurate prediction of protein mechanical strength. To address this challenge, we propose PRESTO, a rapid end-to-end deep learning (DL) model to predict protein resistance to pulling directly from its sequence. By integrating a natural language processing model with simulation-based protein stretching data, we first demonstrate that PRESTO can accurately predict the maximal pulling force, F-max, for given protein sequences with unprecedented efficiency, bypassing the costly steps of conventional methods. Enabled by this rapid prediction capacity, we further find that PRESTO can successfully identify specific mutation locations that may greatly influence protein strength in a biologically plausible manner, such as at the center of polyalanine regions. Finally, we apply our method to design de novo protein sequences by randomly mixing two known sequences at varying ratios. Interestingly, the model predicts that the strength of these mixed proteins follows up-or down-opening banana curves , constructing a protein strength curve that breaks away from the general linear law of mixtures. By discovering key insights and suggesting potential optimal sequences, we demonstrate the versatility of PRESTO primarily as a screening tool in a rapid protein design pipeline. Thereby our model may offer new pathways for protein material research that requires analysis and testing of large-scale novel protein sets, as a discovery tool that can be complemented with other modeling methods, and ultimately, experimental synthesis and testing. (C) 2022 Elsevier Ltd. All rights reserved.

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