Abstract

Ion channels are a class of membrane proteins that attracts a significant amount of basic research, also being potential drug targets. High-throughput identification of these channels is hampered by the low levels of availability of their structures and an observation that use of sequence similarity offers limited predictive quality. Consequently, several machine learning predictors of ion channels from protein sequences that do not rely on high sequence similarity were developed. However, only one of these methods offers a wide scope by predicting ion channels, their types and four major subtypes of the voltage-gated channels. Moreover, this and other existing predictors utilize relatively simple predictive models that limit their accuracy. We propose a novel and accurate predictor of ion channels, their types and the four subtypes of the voltage-gated channels called PSIONplus. Our method combines a support vector machine model and a sequence similarity search with BLAST. The originality of PSIONplus stems from the use of a more sophisticated machine learning model that for the first time in this area utilizes evolutionary profiles and predicted secondary structure, solvent accessibility and intrinsic disorder. We empirically demonstrate that the evolutionary profiles provide the strongest predictive input among new and previously used input types. We also show that all new types of inputs contribute to the prediction. Results on an independent test dataset reveal that PSIONplus obtains relatively good predictive performance and outperforms existing methods. It secures accuracies of 85.4% and 68.3% for the prediction of ion channels and their types, respectively, and the average accuracy of 96.4% for the discrimination of the four ion channel subtypes. Standalone version of PSIONplus is freely available from https://sourceforge.net/projects/psion/

Highlights

  • Ion channels are membrane proteins that facilitate the flow of ions through the lipid membranes [1, 2]

  • Our method considers an empirically selected collection of inputs that for the first time in this area utilizes physiochemical properties of amino acid derived from the input protein chain, position specific scoring matrix (PSSM) profiles generated by PSI-BLAST, and predicted secondary structure, relative solvent accessibility and intrinsic disorder

  • All types of features were selected in at least one predictive model. This demonstrates that the new types of features that we introduce including PSSM profiles, predicted SS, intrinsic disorder (ID) and relative solvent accessibility (RSA) and physiochemical properties of amino acid (AA), contribute to the predictive performance

Read more

Summary

Introduction

Ion channels are membrane proteins that facilitate the flow of ions through the lipid membranes [1, 2]. There are over 300 types of ion channels in living cells [6] They differ in their structures and cellular functions. Ion channels are gated by variety of factors including voltage, ligands, membrane tension, temperature and light [7]. Considering their mechanism of activation, ion channels are mainly classified into the voltage-gated and ligand-gated ion channels [8, 9]. The voltage-gated ion channels can be further classified into several subtypes including potassium (K), sodium (Na), calcium (Ca), anion ion channels, proton channels, transient receptor potential channels and hyperpolarization-activated cyclic nucleotide-gated channels [9]

Objectives
Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.