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DPB-NBFnet: Using neural Bellman-Ford networks to predict DNA-protein binding

DNA is a hereditary material that plays an essential role in micro-organisms and almost all other organisms. Meanwhile, proteins are a vital composition and principal undertaker of microbe movement. Therefore, studying the bindings between DNA and proteins is of high significance from the micro-biol...

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Autores principales: Li, Jing, Zhuo, Linlin, Lian, Xinze, Pan, Shiyao, Xu, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9651613/
https://www.ncbi.nlm.nih.gov/pubmed/36386160
http://dx.doi.org/10.3389/fphar.2022.1018294
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author Li, Jing
Zhuo, Linlin
Lian, Xinze
Pan, Shiyao
Xu, Lei
author_facet Li, Jing
Zhuo, Linlin
Lian, Xinze
Pan, Shiyao
Xu, Lei
author_sort Li, Jing
collection PubMed
description DNA is a hereditary material that plays an essential role in micro-organisms and almost all other organisms. Meanwhile, proteins are a vital composition and principal undertaker of microbe movement. Therefore, studying the bindings between DNA and proteins is of high significance from the micro-biological point of view. In addition, the binding affinity prediction is beneficial for the study of drug design. However, existing experimental methods to identifying DNA-protein bindings are extremely expensive and time consuming. To solve this problem, many deep learning methods (including graph neural networks) have been developed to predict DNA-protein interactions. Our work possesses the same motivation and we put the latest Neural Bellman-Ford neural networks (NBFnets) into use to build pair representations of DNA and protein to predict the existence of DNA-protein binding (DPB). NBFnet is a graph neural network model that uses the Bellman-Ford algorithms to get pair representations and has been proven to have a state-of-the-art performance when used to solve the link prediction problem. After building the pair representations, we designed a feed-forward neural network structure and got a 2-D vector output as a predicted value of positive or negative samples. We conducted our experiments on 100 datasets from ENCODE datasets. Our experiments indicate that the performance of DPB-NBFnet is competitive when compared with the baseline models. We have also executed parameter tuning with different architectures to explore the structure of our framework.
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spelling pubmed-96516132022-11-15 DPB-NBFnet: Using neural Bellman-Ford networks to predict DNA-protein binding Li, Jing Zhuo, Linlin Lian, Xinze Pan, Shiyao Xu, Lei Front Pharmacol Pharmacology DNA is a hereditary material that plays an essential role in micro-organisms and almost all other organisms. Meanwhile, proteins are a vital composition and principal undertaker of microbe movement. Therefore, studying the bindings between DNA and proteins is of high significance from the micro-biological point of view. In addition, the binding affinity prediction is beneficial for the study of drug design. However, existing experimental methods to identifying DNA-protein bindings are extremely expensive and time consuming. To solve this problem, many deep learning methods (including graph neural networks) have been developed to predict DNA-protein interactions. Our work possesses the same motivation and we put the latest Neural Bellman-Ford neural networks (NBFnets) into use to build pair representations of DNA and protein to predict the existence of DNA-protein binding (DPB). NBFnet is a graph neural network model that uses the Bellman-Ford algorithms to get pair representations and has been proven to have a state-of-the-art performance when used to solve the link prediction problem. After building the pair representations, we designed a feed-forward neural network structure and got a 2-D vector output as a predicted value of positive or negative samples. We conducted our experiments on 100 datasets from ENCODE datasets. Our experiments indicate that the performance of DPB-NBFnet is competitive when compared with the baseline models. We have also executed parameter tuning with different architectures to explore the structure of our framework. Frontiers Media S.A. 2022-10-28 /pmc/articles/PMC9651613/ /pubmed/36386160 http://dx.doi.org/10.3389/fphar.2022.1018294 Text en Copyright © 2022 Li, Zhuo, Lian, Pan and Xu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Li, Jing
Zhuo, Linlin
Lian, Xinze
Pan, Shiyao
Xu, Lei
DPB-NBFnet: Using neural Bellman-Ford networks to predict DNA-protein binding
title DPB-NBFnet: Using neural Bellman-Ford networks to predict DNA-protein binding
title_full DPB-NBFnet: Using neural Bellman-Ford networks to predict DNA-protein binding
title_fullStr DPB-NBFnet: Using neural Bellman-Ford networks to predict DNA-protein binding
title_full_unstemmed DPB-NBFnet: Using neural Bellman-Ford networks to predict DNA-protein binding
title_short DPB-NBFnet: Using neural Bellman-Ford networks to predict DNA-protein binding
title_sort dpb-nbfnet: using neural bellman-ford networks to predict dna-protein binding
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9651613/
https://www.ncbi.nlm.nih.gov/pubmed/36386160
http://dx.doi.org/10.3389/fphar.2022.1018294
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