Two scenarios for overcoming drug resistance by co-targeting

Removal of proteins on an essential pathway of a pathogen is expected to prohibit the pathogen from performing a vital function. To disrupt these pathways, we consider a cut set S of simple graph G, where G representing the PPI network of the pathogen. After removing S, if the difference of sizes of...

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Veröffentlicht in:International journal of bioinformatics research and applications Jg. 11; H. 1; S. 72
Hauptverfasser: Taheri, Golnaz, Ayati, Marzieh, Wong, Limsoon, Eslahchi, Changiz
Format: Journal Article
Sprache:Englisch
Veröffentlicht: Switzerland 2015
Schlagworte:
Anti-Bacterial Agents - pharmacology
Bacterial Proteins - metabolism
Computer Simulation
Drug Design
Drug Resistance, Bacterial - drug effects
Drug Resistance, Bacterial - physiology
Models, Biological
Protein Interaction Mapping - methods
Signal Transduction - drug effects
Signal Transduction - physiology
protein protein interaction
balanced bipartitioning
E coli
pathogens
C jejuni
bioinformatics
PPI networks
drug targets
essential pathways
drug resistance
co–targeting
ISSN:1744-5485
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Zusammenfassung:Removal of proteins on an essential pathway of a pathogen is expected to prohibit the pathogen from performing a vital function. To disrupt these pathways, we consider a cut set S of simple graph G, where G representing the PPI network of the pathogen. After removing S, if the difference of sizes of two partitions is high, the probability of existence of a functioning pathway is increased. We need to partition the graph into balanced partitions and approximate it with spectral bipartitioning. We consider two scenarios: in the first, we do not have any information on drug targets; in second, we consider information on drug targets. Our databases are E. coli and C. jejuni. In the first scenario, 20% and 17% of proteins in cut of E. coli and C. jejuni are drug targets and in the second scenario 53% and 63% of proteins in cut are drug targets respectively.
Bibliographie:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
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ISSN:1744-5485
DOI:10.1504/IJBRA.2015.067338