Literature DB >> 34048146

Constraint-based models for dominating protein interaction networks.

Adel A Alofairi1,2, Emad Mabrouk2,3, Ibrahim E Elsemman4.   

Abstract

The minimum dominating set (MDSet) comprises the smallest number of graph nodes, where other graph nodes are connected with at least one MDSet node. The MDSet has been successfully applied to extract proteins that control protein-protein interaction (PPI) networks and to reveal the correlation between structural analysis and biological functions. Although the PPI network contains many MDSets, the identification of multiple MDSets is an NP-complete problem, and it is difficult to determine the best MDSets, enriched with biological functions. Therefore, the MDSet model needs to be further expanded and validated to find constrained solutions that differ from those generated by the traditional models. Moreover, by identifying the critical set of the network, the set of nodes common to all MDSets can be time-consuming. Herein, the authors adopted the minimisation of metabolic adjustment (MOMA) algorithm to develop a new framework, called maximisation of interaction adjustment (MOIA). In MOIA, they provide three models; the first one generates two MDSets with a minimum number of shared proteins, the second model generates constrained multiple MDSets ( k -MDSets), and the third model generates user-defined MDSets, containing the maximum number of essential genes and/or other important genes of the PPI network. In practice, these models significantly reduce the cost of finding the critical set and classifying the graph nodes. Herein, the authors termed the critical set as the k -critical set, where k is the number of MDSets generated by the proposed model. Then, they defined a new set of proteins called the ( k - 1 ) -critical set, where each node belongs to ( k - 1 ) MDSets. This set has been shown to be as important as the k -critical set and contains many essential genes, transcription factors, and protein kinases as the k -critical set. The ( k - 1 ) -critical set can be used to extend the search for drug target proteins. Based on the performance of the MOIA models, the authors believe the proposed methods contribute to answering key questions about the MDSets of PPI networks, and their results and analysis can be extended to other network types.
© 2021 The Authors. IET Systems Biology published by John Wiley & Sons Ltd on behalf of The Institution of Engineering and Technology.

Entities:  

Mesh:

Substances:

Year:  2021        PMID: 34048146      PMCID: PMC8675806          DOI: 10.1049/syb2.12021

Source DB:  PubMed          Journal:  IET Syst Biol        ISSN: 1751-8849            Impact factor:   1.615


  35 in total

1.  Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources.

Authors:  Da Wei Huang; Brad T Sherman; Richard A Lempicki
Journal:  Nat Protoc       Date:  2009       Impact factor: 13.491

2.  Computational methods for identifying the critical nodes in biological networks.

Authors:  Xiangrong Liu; Zengyan Hong; Juan Liu; Yuan Lin; Alfonso Rodríguez-Patón; Quan Zou; Xiangxiang Zeng
Journal:  Brief Bioinform       Date:  2020-03-23       Impact factor: 11.622

3.  Controllability in protein interaction networks.

Authors:  Stefan Wuchty
Journal:  Proc Natl Acad Sci U S A       Date:  2014-04-28       Impact factor: 11.205

4.  idenPC-MIIP: identify protein complexes from weighted PPI networks using mutual important interacting partner relation.

Authors:  Zhourun Wu; Qing Liao; Bin Liu
Journal:  Brief Bioinform       Date:  2021-03-22       Impact factor: 11.622

5.  Dominating biological networks.

Authors:  Tijana Milenković; Vesna Memišević; Anthony Bonato; Nataša Pržulj
Journal:  PLoS One       Date:  2011-08-26       Impact factor: 3.240

6.  DrugBank: a comprehensive resource for in silico drug discovery and exploration.

Authors:  David S Wishart; Craig Knox; An Chi Guo; Savita Shrivastava; Murtaza Hassanali; Paul Stothard; Zhan Chang; Jennifer Woolsey
Journal:  Nucleic Acids Res       Date:  2006-01-01       Impact factor: 16.971

7.  Pan-cancer network analysis identifies combinations of rare somatic mutations across pathways and protein complexes.

Authors:  Mark D M Leiserson; Fabio Vandin; Hsin-Ta Wu; Jason R Dobson; Jonathan V Eldridge; Jacob L Thomas; Alexandra Papoutsaki; Younhun Kim; Beifang Niu; Michael McLellan; Michael S Lawrence; Abel Gonzalez-Perez; David Tamborero; Yuwei Cheng; Gregory A Ryslik; Nuria Lopez-Bigas; Gad Getz; Li Ding; Benjamin J Raphael
Journal:  Nat Genet       Date:  2014-12-15       Impact factor: 38.330

8.  YEASTRACT: an upgraded database for the analysis of transcription regulatory networks in Saccharomyces cerevisiae.

Authors:  Miguel C Teixeira; Pedro T Monteiro; Margarida Palma; Catarina Costa; Cláudia P Godinho; Pedro Pais; Mafalda Cavalheiro; Miguel Antunes; Alexandre Lemos; Tiago Pedreira; Isabel Sá-Correia
Journal:  Nucleic Acids Res       Date:  2018-01-04       Impact factor: 16.971

Review 9.  Genome, transcriptome and proteome: the rise of omics data and their integration in biomedical sciences.

Authors:  Claudia Manzoni; Demis A Kia; Jana Vandrovcova; John Hardy; Nicholas W Wood; Patrick A Lewis; Raffaele Ferrari
Journal:  Brief Bioinform       Date:  2018-03-01       Impact factor: 11.622

10.  Quantitative network mapping of the human kinome interactome reveals new clues for rational kinase inhibitor discovery and individualized cancer therapy.

Authors:  Feixiong Cheng; Peilin Jia; Quan Wang; Zhongming Zhao
Journal:  Oncotarget       Date:  2014-06-15
View more
  1 in total

1.  Constraint-based models for dominating protein interaction networks.

Authors:  Adel A Alofairi; Emad Mabrouk; Ibrahim E Elsemman
Journal:  IET Syst Biol       Date:  2021-05-28       Impact factor: 1.615

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.