Semantical and Geometrical Protein Encoding Toward Enhanced Bioactivity and Thermostability

Author:

Tan Yang123,Zhou Bingxin14,Zheng Lirong1,Fan Guisheng2,Hong Liang1453

Affiliation:

1. Institute of Natural Sciences, Shanghai Jiao Tong University

2. School of Information Science and Engineering, East China University of Science and Technology

3. Shanghai Artificial Intelligence Laboratory

4. Shanghai National Center for Applied Mathematics (SJTU center), Shanghai Jiao Tong University

5. Zhangjiang Institute for Advanced Study, Shanghai Jiao Tong University

Abstract

Protein engineering is a pivotal aspect of synthetic biology, involving the modification of amino acids within existing protein sequences to achieve novel or enhanced functionalities and physical properties. Accurate prediction of protein variant effects requires a thorough understanding of protein sequence, structure, and function. Deep learning methods have demonstrated remarkable performance in guiding protein modification for improved functionality. However, existing approaches predominantly rely on protein sequences, which face challenges in efficiently encoding the geometric aspects of amino acids’ local environment and often fall short in capturing crucial details related to protein folding stability, internal molecular interactions, and bio-functions. Furthermore, there lacks a fundamental evaluation for developed methods in predicting protein thermostability, although it is a key physical property that is frequently investigated in practice. To address these challenges, this paper introduces a novel pre-training framework that integrates sequential and geometric encoders for protein primary and tertiary structures. This framework guides mutation directions toward desired traits by simulating natural selection on wild-type proteins and evaluates variant effects based on their fitness to perform specific functions. We assess the proposed approach using three benchmarks comprising over 300 deep mutational scanning assays. The prediction results showcase exceptional performance across extensive experiments when compared to other zero-shot learning methods, all while maintaining a minimal cost in terms of trainable parameters. This study not only proposes an effective framework for more accurate and comprehensive predictions to facilitate efficient protein engineering, but also enhances the in silico assessment system for future deep learning models to better align with empirical requirements. The PyTorch implementation are available at https://github.com/tyang816/ProtSSN.

Publisher

eLife Sciences Publications, Ltd

Reference64 articles.

1. Rational design of a conformation-specific antibody for the quantification of Aβ oligomers;Proceedings of the National Academy of Sciences,2020

2. ProteinBERT: A universal deep-learning model of protein sequence and function;Bioinformatics,2022

3. BERT: Pre-training of deep bidirectional transformers for language understanding,2018

4. High-resolution Cryo-EM: the nuts and bolts;Current Opinion in Structural Biology,2017

5. ProtTrans: Toward Understanding the Language of Life Through Self-Supervised Learning;IEEE Transactions on Pattern Analysis and Machine Intelligence,2022

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