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<records>

  <record>
    <language>eng</language>
          <publisher>Oriental Scientific Publishing Company</publisher>
        <journalTitle>Biosciences Biotechnology Research Asia</journalTitle>
          <issn>0973-1245</issn>
            <publicationDate>2016-06-22</publicationDate>
    
        <volume>12</volume>
        <issue>Spl.Edn.2</issue>

 
    <startPage>725</startPage>
    <endPage>730</endPage>

	 
      <doi>10.13005/bbra/2253</doi>
        <publisherRecordId>13646</publisherRecordId>
    <documentType>article</documentType>
    <title language="eng">Designing, Optimizing, and Structure Prediction of Chimeric Protein CTB-IpaD for Expression in E.coli</title>

    <authors>
	 


      <author>
       <name>Seyed Mohammad Gheibi Hayat</name>

 
		
	<affiliationId>1</affiliationId>
      </author>
    

	 


      <author>
       <name>Azam Sadeghinia</name>


		
	<affiliationId>2</affiliationId>

      </author>
    

	 


      <author>
       <name>Babak Elyasifar</name>

		
	<affiliationId>3</affiliationId>
      </author>
    

	 


      <author>
       <name>Ghasem Abbaszadeh-Goudarzi</name>

		
	<affiliationId>4</affiliationId>
      </author>
    


	 


      <author>
       <name>Zahra Adeli</name>

		
	<affiliationId>5</affiliationId>
      </author>
    


	 


      <author>
       <name>Somaieh Salimi</name>

		
	<affiliationId>6</affiliationId>
      </author>
    
    </authors>
    
	    <affiliationsList>
	    
		
		<affiliationName affiliationId="1">Young Researchers and Elite Club, Andimeshk Branch, Islamic Azad University, Andimeshk, Iran.</affiliationName>
    

		
		<affiliationName affiliationId="2">Department of Cardiology, Faculty of Medicine, Dezful University of Medical Sciences, Dezful, Iran.</affiliationName>
    
		
		<affiliationName affiliationId="3">Department of Drug Biotechnology, Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.</affiliationName>
    
		
		<affiliationName affiliationId="4">Department of Medical Biotechnology, Faculty of Advanced Technologies in Medicine, Tehran University of medical Sciences, Tehran, Iran.</affiliationName>
    
		
		<affiliationName affiliationId="5">Department of Microbiology, Islamic Azad University, Damghan Branch, Damghan, Iran</affiliationName>
    
		
		<affiliationName affiliationId="6">Department of Marine Biology, Faculty of Marine Science, Chabahar Marine University, Chabahar, Iran.</affiliationName>
    
	  </affiliationsList>






    <abstract language="eng">The most common cause of diarrhea is Shigella and no vaccine has been found
to provide protection against it. IpaD play an important role in invasion, infection, and
pathogenesis caused by Shigella. This protein has been one of the most important protein
for shigella vaccine candidate. This study aims to link the gene sequence IpaD and CTB
with In-silico analysis. Nucleotide sequences were obtained from NCBI database and
optimized. Sequences were fused together by a flexible linker in order to find the best
epitope exposing chimeric antigen. After Protein half-life and instability index were
determined, and then the prediction of the secondary structure and the three-dimensional
structure was analyzed and also immunodominant linear B-cell epitopes were also settled
at the final step. Codons were changed with respect to codon bias of E.coli and the GC
content was changed to an optimal level. Inappropriate structures of RNA were removed.
However, these changes led to a prolonged half-life and increased mRNA expression of
the recombinant protein. Sequences of the chimeric gene was optimized based on codon
usage pattern, In-silico analysis represented that sequence can have a high expression in
E.coli and designed to enhance the expression of proteins which contain rare codons at
high frequency. (EAAAK) 4 hydrophobic linkers could prevent the domain interactions
of the chimeric protein. Chimeric protein can be a good candidate in immunogenicity
study to produce an effective vaccine.</abstract>

    <fullTextUrl format="html">https://www.biotech-asia.org/vol12_nospl_edn2/designing-optimizing-and-structure-prediction-of-chimeric-protein-ctb-ipad-for-expression-in-e-coli/</fullTextUrl>



      <keywords language="eng">
        <keyword>Shigella dysenteriae; IpaD protein; B subunit cholera toxin; Bioinformatics</keyword>
      </keywords>

  </record>
</records>