Large-scale comparative assessment of computational predictors for lysine post-translational modification sites

Author:

Chen Zhen1,Liu Xuhan2,Li Fuyi34,Li Chen35,Marquez-Lago Tatiana67,Leier André67,Akutsu Tatsuya8,Webb Geoffrey I9,Xu Dakang1011,Smith Alexander Ian34,Li Lei1ORCID,Chou Kuo-Chen1213,Song Jiangning349

Affiliation:

1. School of Basic Medical Science, Qingdao University, Dengzhou Road, Qingdao, Shandong, China

2. Medicinal Chemistry, Leiden Academic Centre for Drug Research,Einsteinweg, Leiden, The Netherlands

3. Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Faculty of Medicine, Monash University, Melbourne, VIC, Australia

4. ARC Centre of Excellence in Advanced Molecular Imaging, Monash University, Melbourne, VIC, Australia

5. Institute of Molecular Systems Biology, ETH Zürich,Auguste-Piccard-Hof, Zürich, Switzerland

6. Department of Genetics, School of Medicine, University of Alabama at Birmingham, AL, USA

7. Department of Cell, Developmental and Integrative Biology, School of Medicine, University of Alabama at Birmingham, AL, USA

8. Bioinformatics Center, Institute for Chemical Research,Kyoto University, Uji, Kyoto, Japan

9. Monash Centre for Data Science, Faculty of Information Technology, Monash University, Melbourne, VIC, Australia

10. Faculty of Medical Laboratory Science, Ruijin Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China

11. Department of Molecular and Translational Science, Faculty of Medicine, Hudson Institute of Medical Research, Monash University, Melbourne, VIC, Australia

12. Gordon Life Science Institute, Boston, MA, USA

13. Center for Informational Biology, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, China

Abstract

Abstract Lysine post-translational modifications (PTMs) play a crucial role in regulating diverse functions and biological processes of proteins. However, because of the large volumes of sequencing data generated from genome-sequencing projects, systematic identification of different types of lysine PTM substrates and PTM sites in the entire proteome remains a major challenge. In recent years, a number of computational methods for lysine PTM identification have been developed. These methods show high diversity in their core algorithms, features extracted and feature selection techniques and evaluation strategies. There is therefore an urgent need to revisit these methods and summarize their methodologies, to improve and further develop computational techniques to identify and characterize lysine PTMs from the large amounts of sequence data. With this goal in mind, we first provide a comprehensive survey on a large collection of 49 state-of-the-art approaches for lysine PTM prediction. We cover a variety of important aspects that are crucial for the development of successful predictors, including operating algorithms, sequence and structural features, feature selection, model performance evaluation and software utility. We further provide our thoughts on potential strategies to improve the model performance. Second, in order to examine the feasibility of using deep learning for lysine PTM prediction, we propose a novel computational framework, termed MUscADEL (Multiple Scalable Accurate Deep Learner for lysine PTMs), using deep, bidirectional, long short-term memory recurrent neural networks for accurate and systematic mapping of eight major types of lysine PTMs in the human and mouse proteomes. Extensive benchmarking tests show that MUscADEL outperforms current methods for lysine PTM characterization, demonstrating the potential and power of deep learning techniques in protein PTM prediction. The web server of MUscADEL, together with all the data sets assembled in this study, is freely available at http://muscadel.erc.monash.edu/. We anticipate this comprehensive review and the application of deep learning will provide practical guide and useful insights into PTM prediction and inspire future bioinformatics studies in the related fields.

Funder

Australian Research Council

National Natural Science Foundation of China

National Health and Medical Research Council

National Institute of Allergy and Infectious Diseases

Monash University

Kyoto University

Institute of the School of Medicine

University of Alabama at Birmingham

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Information Systems

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