Isolation and Characterization of Novel Phage Displayed scFv Fragment for Human Tumor Necrosis Factor Alpha and Molecular Docking Analysis of Their Interactions

AuthorHossein Safarpouren
AuthorMorteza Shahmirzaieen
AuthorElham Rezaeeen
AuthorMahmood Baratien
AuthorMohammad Reza Safarnejaden
AuthorFarshad H. Shirazien
Issued Date2018-04-30en
AbstractTumor necrosis factor alpha (TNF-α) expression amplifies to excess amounts in several disorders such as rheumatoid arthritis and psoriasis. Although, Anti-TNF biologics have revolutionized the treatment of these autoimmune diseases, formation of anti-drug antibodies (ADA) has dramatically affected their use. The next generation antibodies (e.g. Fab, scFv) have not only reduced resulted immunogenicity, but also proved several benefits including better tumor penetration and more rapid blood clearance. Using affinity selection procedures in this study, a scFv antibody clone was isolated from naïve Tomlinson I phage display library that specifically recognizes and binds to TNF-α. The TNF-α recombinant protein was expressed in genetically engineered Escherichia coli SHuffle® T7 Express, for the first time, which is able to express disulfide-bonded recombinant proteins into their correctly folded states. ELISA-based affinity characterization results indicated that the isolated novel 29.2 kDa scFv binds TNF-α with suitable affinity. In-silico homology modeling study using ‘ModWeb’ as well as molecular docking study using Hex program confirmed the scFv and TNF-α interactions with a scFv-TNF- α binding energy of around -593 kj/mol which is well in agreement with our ELSIA results. The cloned scFv antibody may be potentially useful for research and therapeutic applications in the future.en
DOIhttps://doi.org/10.22037/ijpr.2018.2229en
KeywordHomology modelingen
KeywordMolecular dockingen
KeywordPhage displayen
KeywordSHuffle<sup>®</sup> T7 Expressen
KeywordSingle chain variable fragment (scFv)en
KeywordTumor necrosis factor alphaen
PublisherBrieflandsen
TitleIsolation and Characterization of Novel Phage Displayed scFv Fragment for Human Tumor Necrosis Factor Alpha and Molecular Docking Analysis of Their Interactionsen
TypeOriginal Articleen

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