HLPpred-Fuse: improved and robust prediction of hemolytic peptide and its activity by fusing multiple feature representation

Abstract Motivation Therapeutic peptides failing at clinical trials could be attributed to their toxicity profiles like hemolytic activity, which hamper further progress of peptides as drug candidates. The accurate prediction of hemolytic peptides (HLPs) and its activity from the given peptides is o...

Full description

Saved in:
Bibliographic Details
Published inBioinformatics Vol. 36; no. 11; pp. 3350 - 3356
Main Authors Hasan, Md Mehedi, Schaduangrat, Nalini, Basith, Shaherin, Lee, Gwang, Shoombuatong, Watshara, Manavalan, Balachandran
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.06.2020
Online AccessGet full text

Cover

Loading…
More Information
Summary:Abstract Motivation Therapeutic peptides failing at clinical trials could be attributed to their toxicity profiles like hemolytic activity, which hamper further progress of peptides as drug candidates. The accurate prediction of hemolytic peptides (HLPs) and its activity from the given peptides is one of the challenging tasks in immunoinformatics, which is essential for drug development and basic research. Although there are a few computational methods that have been proposed for this aspect, none of them are able to identify HLPs and their activities simultaneously. Results In this study, we proposed a two-layer prediction framework, called HLPpred-Fuse, that can accurately and automatically predict both hemolytic peptides (HLPs or non-HLPs) as well as HLPs activity (high and low). More specifically, feature representation learning scheme was utilized to generate 54 probabilistic features by integrating six different machine learning classifiers and nine different sequence-based encodings. Consequently, the 54 probabilistic features were fused to provide sufficiently converged sequence information which was used as an input to extremely randomized tree for the development of two final prediction models which independently identify HLP and its activity. Performance comparisons over empirical cross-validation analysis, independent test and case study against state-of-the-art methods demonstrate that HLPpred-Fuse consistently outperformed these methods in the identification of hemolytic activity. Availability and implementation For the convenience of experimental scientists, a web-based tool has been established at http://thegleelab.org/HLPpred-Fuse. Contact glee@ajou.ac.kr or watshara.sho@mahidol.ac.th or bala@ajou.ac.kr Supplementary information Supplementary data are available at Bioinformatics online.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1367-4803
1460-2059
1367-4811
DOI:10.1093/bioinformatics/btaa160