<?xml version="1.0"?>
<Articles JournalTitle="Iranian Journal of Public Health">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Iranian Journal of Public Health</JournalTitle>
      <Issn>2251-6085</Issn>
      <Volume>44</Volume>
      <Issue>12</Issue>
      <PubDate PubStatus="epublish">
        <Year>2015</Year>
        <Month>12</Month>
        <Day>22</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Optimized Expression and Purification of Humbug in Pichia pastoris and Its Monoclonal Antibody Preparation</title>
    <FirstPage>1632</FirstPage>
    <LastPage>1642</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Ting</FirstName>
        <LastName>HUYAN</LastName>
      </Author>
      <Author>
        <FirstName>Ruihua</FirstName>
        <LastName>TANG</LastName>
      </Author>
      <Author>
        <FirstName>Jing</FirstName>
        <LastName>LI</LastName>
      </Author>
      <Author>
        <FirstName>Qi</FirstName>
        <LastName>LI</LastName>
      </Author>
      <Author>
        <FirstName>Xiaoping</FirstName>
        <LastName>XUE</LastName>
      </Author>
      <Author>
        <FirstName>Hui</FirstName>
        <LastName>YANG</LastName>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>12</Month>
        <Day>22</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2015</Year>
        <Month>12</Month>
        <Day>22</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Background: The humbug gene is a truncated isoform of Aspartyl &#x3B2;-hydroxylase (ASPH) gene that is overexpressed in many human malignancies. In recent years, since humbug has received increasing attention, it is considered as a potential therapeutic molecular target. Therefore, it is necessary for preparing humbug protein and its monoclonal antibody to investigate its structure and function.
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Method: The optimized humbug gene, synthesized by Genscript in Nanjing, China on December 21st 2013, was expressed in Pichia pastoris cells that were cultured in a 10-L bioreactor. The recombinant protein was further obtained and puri&#xFB01;ed by using ion exchange chromatography and Sephadex G75. The humbug protein was used to immunize Balb/c mice to generate the monoclonal antibodies. The specificity and sensitivity of the monoclonal antibodies were assessed by indirect enzyme-linked immunosorbent assay. Finally, the humbug monoclonal antibodies were used to detect the expression of humbug in several tumor cell lines via indirect immunofluorescence.
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Results: Firstly, the recombinant humbug was expressed in P. pastoris successfully and efficiently by using a gene-optimized strategy. Secondly, the purification process of humbug was established via multiple chromatography methods. In addition, four monoclonal antibodies against humbug were obtained from the immunized Balb/c mice, and the result of indirect immunofluorescence was indicated that the humbug monoclonal antibody showed the high affinity with humbug protein, which expressed in several tumor cell lines.
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Conclusion: The over-expression of recombinant humbug provides adequate sources for its structural study and the preparation of the humbug-specific monoclonal antibody can potentially be used in tumor initial diagnosis and immunotherapy.
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Keywords: Humbug, Fermentation, Pichia pastoris, Monoclonal antibody, Tumor diagnosis
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&#xA0;</abstract>
    <web_url>https://ijph.tums.ac.ir/index.php/ijph/article/view/5559</web_url>
    <pdf_url>https://ijph.tums.ac.ir/index.php/ijph/article/download/5559/4551</pdf_url>
  </Article>
</Articles>
