P. Milazzo, R. Gori, A. Micheli, Lucia Nasti, Marco Podda
{"title":"In silico modeling of biochemical pathways","authors":"P. Milazzo, R. Gori, A. Micheli, Lucia Nasti, Marco Podda","doi":"10.4081/bse.2021.142","DOIUrl":null,"url":null,"abstract":"We present in silico modeling methods for the investigation of dynamical properties of biochemical pathways, that are chemical reaction networks underlying cell functioning. Since pathways are (complex) dynamical systems, in-silico models are often studied by applying numerical integration techniques for Ordinary Differential Equations (ODEs), or stochastic simulation algorithms. However, these techniques require a rather accurate knowledge of the kinetic parameters of the modeled chemical reactions. Moreover, in the case of very complex reaction networks, in silico analysis can become unfeasible from the computational viewpoint. Consequently, in the last few years several approaches have been proposed that focus on estimating or predicting dynamical properties from the analysis of the structure of the biochemical pathway. This means that the analysis focuses more on the interaction patterns than on the kinetic parameters, and this usually makes it possible to deduce the role of each molecule and how each molecule qualitatively influences each other, by abstracting away from quantitative details about concentrations and reaction rates.","PeriodicalId":89077,"journal":{"name":"Annual ORNL Biomedical Science and Engineering Center Conference. ORNL Biomedical Science and Engineering Center Conference","volume":"62 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annual ORNL Biomedical Science and Engineering Center Conference. ORNL Biomedical Science and Engineering Center Conference","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4081/bse.2021.142","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
We present in silico modeling methods for the investigation of dynamical properties of biochemical pathways, that are chemical reaction networks underlying cell functioning. Since pathways are (complex) dynamical systems, in-silico models are often studied by applying numerical integration techniques for Ordinary Differential Equations (ODEs), or stochastic simulation algorithms. However, these techniques require a rather accurate knowledge of the kinetic parameters of the modeled chemical reactions. Moreover, in the case of very complex reaction networks, in silico analysis can become unfeasible from the computational viewpoint. Consequently, in the last few years several approaches have been proposed that focus on estimating or predicting dynamical properties from the analysis of the structure of the biochemical pathway. This means that the analysis focuses more on the interaction patterns than on the kinetic parameters, and this usually makes it possible to deduce the role of each molecule and how each molecule qualitatively influences each other, by abstracting away from quantitative details about concentrations and reaction rates.