<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Medical Journal of the Islamic Republic Of Iran</title>
<title_fa>مجله پزشکی جمهوری اسلامی ایران</title_fa>
<short_title>Med J Islam Repub Iran</short_title>
<subject>Medical Sciences</subject>
<web_url>http://mjiri.iums.ac.ir</web_url>
<journal_hbi_system_id>2</journal_hbi_system_id>
<journal_hbi_system_user>journal2</journal_hbi_system_user>
<journal_id_issn>1016-1430</journal_id_issn>
<journal_id_issn_online>2251-6840</journal_id_issn_online>
<journal_id_pii>8</journal_id_pii>
<journal_id_doi>10.18869/mjiri</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid>14</journal_id_sid>
<journal_id_nlai>8888</journal_id_nlai>
<journal_id_science>13</journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1383</year>
	<month>6</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2004</year>
	<month>9</month>
	<day>1</day>
</pubdate>
<volume>18</volume>
<number>2</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>PURIFICATION AND CHARACTERIZATION OF CELL WALLMANNOPRO TEINS OF CANDIDA ALB/CANS USING INTACT CELL METHOD </title>
	<subject_fa> Clinical Biochemistry</subject_fa>
	<subject> Clinical Biochemistry</subject>
	<content_type_fa>Original Research: Basic Science in Medicine</content_type_fa>
	<content_type>Original Research: Basic Science in Medicine</content_type>
	<abstract_fa></abstract_fa>
	<abstract>Virulence of the opportunistic yeast, Candida albieans, involves the interplay of
many complex changes including the yeast-hyphae transition, which mainly involves
protein changes. Cell wall mannoproteins are found to be the main cause of adherence
of C. albieans to epithel ial cells in the first step of an infection process. In the present
study, cell wall mannoproteins of intact yeast were purified using a simple treatment of
yeast with mercaptoethanol and sodium dodecyl sulfate followed by Concanavalin A
chromatography. Both electrophoretic analysis of the column effluent and Western blot
analysis using polyclonal and monoclonal antibodies showed the presence of
mannoproteins with molecular weight in the range of30-50 kDa. Dot blot analysis of
the purified antigen with the polyclonal and monoclonal antibodies prepared in this
study showed that outer membrane mannoprotein antigens were obtained successfully
following the above simple purification strategy
</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Candida albicans, Mannoproteins, Purification, Characterization</keyword>
	<start_page>167</start_page>
	<end_page>172</end_page>
	<web_url>http://mjiri.iums.ac.ir/browse.php?a_code=A-10-298-97&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Z</first_name>
	<middle_name></middle_name>
	<last_name>FARAHNEJAD</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>20031947532846003588</code>
	<orcid>20031947532846003588</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>From the Department 0f Medical Mycology</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>MJ</first_name>
	<middle_name></middle_name>
	<last_name>RASAEE</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>rasaee _m@modares.ac.ir.</email>
	<code>20031947532846003589</code>
	<orcid>20031947532846003589</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Clinical Biochemistry</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>H</first_name>
	<middle_name></middle_name>
	<last_name>YADEGARI</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>20031947532846003590</code>
	<orcid>20031947532846003590</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>From the Department 0f Medical Mycology</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>M</first_name>
	<middle_name></middle_name>
	<last_name>FROUZANDEH MOGHADAM</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>20031947532846003591</code>
	<orcid>20031947532846003591</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department o/Medical Biotechnology, School of Medical Sciences, Tarbiat Modarres University, Tehran. I.R. Iran </affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
