Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/70212
Full metadata record
DC FieldValueLanguage
dc.contributor.authorPhasit Charoenkwanen_US
dc.contributor.authorJanchai Yanaen_US
dc.contributor.authorNalini Schaduangraten_US
dc.contributor.authorChanin Nantasenamaten_US
dc.contributor.authorMd Mehedi Hasanen_US
dc.contributor.authorWatshara Shoombuatongen_US
dc.date.accessioned2020-10-14T08:25:39Z-
dc.date.available2020-10-14T08:25:39Z-
dc.date.issued2020-07-01en_US
dc.identifier.issn10898646en_US
dc.identifier.issn08887543en_US
dc.identifier.other2-s2.0-85082798572en_US
dc.identifier.other10.1016/j.ygeno.2020.03.019en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85082798572&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/70212-
dc.description.abstract© 2020 Elsevier Inc. In general, hydrolyzed proteins, plant-derived alkaloids and toxins displays unpleasant bitter taste. Thus, the perception of bitter taste plays a crucial role in protecting animals from poisonous plants and environmental toxins. Therapeutic peptides have attracted great attention as a new drug class. The successful identification and characterization of bitter peptides are essential for drug development and nutritional research. Owing to the large volume of peptides generated in the post-genomic era, there is an urgent need to develop computational methods for rapidly and effectively discriminating bitter peptides from non-bitter peptides. To the best of our knowledge, there is yet no computational model for predicting and analyzing bitter peptides using sequence information. In this study, we present for the first time a computational model called the iBitter-SCM that can predict the bitterness of peptides directly from their amino acid sequence without any dependence on their functional domain or structural information. iBitter-SCM is a simple and effective method that was built using the scoring card method (SCM) with estimated propensity scores of amino acids and dipeptides. Our benchmarking results demonstrated that iBitter-SCM achieved an accuracy and Matthews coefficient correlation of 84.38% and 0.688, respectively, on the independent dataset. Rigorous independent test indicated that iBitter-SCM was superior to those of other widely used machine-learning classifiers (e.g. k-nearest neighbor, naive Bayes, decision tree and random forest) owing to its simplicity, interpretability and implementation. Furthermore, the analysis of estimated propensity scores of amino acids and dipeptides were performed to provide a better understanding of the biophysical and biochemical properties of bitter peptides. For the convenience of experimental scientists, a web server is provided publicly at http://camt.pythonanywhere.com/iBitter-SCM. It is anticipated that iBitter-SCM can serve as an important tool to facilitate the high-throughput prediction and de novo design of bitter peptides.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleiBitter-SCM: Identification and characterization of bitter peptides using a scoring card method with propensity scores of dipeptidesen_US
dc.typeJournalen_US
article.title.sourcetitleGenomicsen_US
article.volume112en_US
article.stream.affiliationsChiang Mai Rajabhat Universityen_US
article.stream.affiliationsKyushu Institute of Technologyen_US
article.stream.affiliationsMahidol Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

Files in This Item:
There are no files associated with this item.


Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.