﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Tabriz University of Medical Sciences</PublisherName>
      <JournalTitle>Advanced Pharmaceutical Bulletin</JournalTitle>
      <Issn>2228-5881</Issn>
      <Volume>5</Volume>
      <Issue>5</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2015</Year>
        <Month>12</Month>
        <DAY>31</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Identification of Novel Single Chain Fragment Variable Antibodies Against TNF-α Using Phage Display Technology</ArticleTitle>
    <FirstPage>661</FirstPage>
    <LastPage>666</LastPage>
    <ELocationID EIdType="doi">10.15171/apb.2015.090</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Ali Akbar</FirstName>
        <LastName>Alizadeh</LastName>
      </Author>
      <Author>
        <FirstName>Maryam</FirstName>
        <LastName>Hamzeh-Mivehroud</LastName>
      </Author>
      <Author>
        <FirstName>Siavoush</FirstName>
        <LastName>Dastmalchi</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.15171/apb.2015.090</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>19</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2015</Year>
        <Month>11</Month>
        <Day>01</Day>
      </PubDate>
    </History>
    <Abstract>Purpose: Tumor necrosis factor alpha (TNF-α) is an inflammatory cytokine, involved in both physiological and pathological pathways. Because of central role of TNF-α in pathogenesis of inflammatory diseases, in the current study, we aimed to identify novel scFv antibodies against TNF-α using phage display technology. Methods: Using libraries composed of phagemid displaying scFv antibodies, four rounds of biopanning against TNF-α were carried out, which led to identification of scFvs capable of binding to TNF-α. The scFv antibody with appropriate binding affinity towards TNF-α, was amplified and used in ELISA experiment. Results: Titration of phage achieved from different rounds of biopanning showed an enrichment of specific anti-TNF-α phages during biopanning process. Using ELISA experiment, a binding constant (Kd) of 1.11 ± 0.32 nM was determined for the phage displaying J48 scFv antibody. Conclusion: The findings in the current work revealed that the identified novel scFv antibody displayed at the N-terminal of minor coat proteins of phagemid binds TNF-α with suitable affinity. However, the soluble form of the antibody is needed to be produced and evaluated in more details regarding its binding properties to TNF-α.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">TNF-α</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Phage display</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Single chain variable fragment</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Antibody library</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>