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dc.contributor.authorAlizadeh, AA
dc.contributor.authorHamzeh-Mivehroud, M
dc.contributor.authorFarajzadeh, M
dc.contributor.authorDastmalchi, S
dc.date.accessioned2018-08-26T08:57:22Z
dc.date.available2018-08-26T08:57:22Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/54565
dc.description.abstractThe aim of this study was to identify novel TNF-? blocking peptide(s) using phage display technology. Two novel 7-mer TNF-? binding peptides P51 and P52 with Kd values of 1.47 and 0.51 nM were identified. Phage particles displaying P51 and P52 peptides at 0.318 nM concentration prevent cytotoxic effect of TNF-? on L929 cells by 8.2% and 16.15%, respectively. Synthesized P51 and P52 peptides also inhibited TNF-? induced cytotoxicity with IC50 values of 25.15 آ± 2.18 and 7.08 آ± 2.24 ?M, respectively. The result of RT-PCR also supports the inhibitory activity of the identified peptides, where P51 and P52 significantly inhibit the inductive effect of TNF-? on I?B-? mRNA levels. The inhibitory effects of the peptides were attributed to their abilities of binding at the inter-subunit interfaces leading to TNF-? dissociation. The results of molecular docking studies revealed that the peptides-TNF-? complexes are mostly stabilized by hydrophobic contacts. é 2016 Elsevier B.V.
dc.language.isoEnglish
dc.relation.ispartofEuropean Journal of Pharmaceutical Sciences
dc.subjectI kappa B alpha
dc.subjectmessenger RNA
dc.subjectprotein p51
dc.subjectprotein p52
dc.subjecttumor necrosis factor
dc.subjectpeptide
dc.subjectpeptide library
dc.subjectprotein binding
dc.subjecttumor necrosis factor
dc.subjectanimal cell
dc.subjectArticle
dc.subjectcomputer model
dc.subjectconcentration (parameters)
dc.subjectcontrolled study
dc.subjectcytotoxicity
dc.subjectdissociation
dc.subjectdrug binding
dc.subjectdrug identification
dc.subjectIC50
dc.subjectL929 cell line
dc.subjectmolecular docking
dc.subjectnonhuman
dc.subjectphage display
dc.subjectpriority journal
dc.subjectanimal
dc.subjectantagonists and inhibitors
dc.subjectcell surface display
dc.subjectchemical model
dc.subjectchemistry
dc.subjectcomputer simulation
dc.subjectgenetics
dc.subjecthuman
dc.subjectJurkat cell line
dc.subjectmetabolism
dc.subjectmouse
dc.subjectpeptide library
dc.subjectphysiology
dc.subjectprocedures
dc.subjectprotein secondary structure
dc.subjectprotein tertiary structure
dc.subjectAnimals
dc.subjectCell Surface Display Techniques
dc.subjectComputer Simulation
dc.subjectHumans
dc.subjectJurkat Cells
dc.subjectMice
dc.subjectModels, Chemical
dc.subjectPeptide Library
dc.subjectPeptides
dc.subjectProtein Binding
dc.subjectProtein Structure, Secondary
dc.subjectProtein Structure, Tertiary
dc.subjectTumor Necrosis Factor-alpha
dc.titleIdentification of novel peptides against TNF-? using phage display technique and in silico modeling of their modes of binding
dc.typeArticle
dc.citation.volume96
dc.citation.spage490
dc.citation.epage498
dc.citation.indexScopus
dc.identifier.DOIhttps://doi.org/10.1016/j.ejps.2016.10.005


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