Molecular Cloning and Expression of the Leishmania Tropica Kmp-11 Gene
Kinetoplastid membrane protein-11 (KMP-11) is a small protein of 11 kDa present in all kinetoplastid protozoa studded so far. This protein which is highly expressed in all stages of the Leishmania life cycle is considered a potential candidate for a leishmaniasis vaccine against many leishmania spec...
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creator | Abbady , Abdul Qader A Meriee , Mouayad Soukkarieh , Chadi |
description | Kinetoplastid membrane protein-11 (KMP-11) is a small protein of 11 kDa present in all kinetoplastid
protozoa studded so far. This protein which is highly expressed in all stages of
the Leishmania life cycle is considered a potential candidate for a leishmaniasis vaccine
against many leishmania species. KMP-11 has been recently described in Leishmania tropica.
In the present study, the KMP-11 gene was extracted from L. tropica by PCR using two
oligonucleotide primers designed to amplify the entire coding region of this gene. Then, the
purified PCR products were successfully ligated into a high expression vector the pRSETGFP.
This expression vector provides the opportunity to clone the desired insert as a fusion
protein with a GFP and a tag, polyhistidine region. The GFP use as a carrier to improve immune
response and the polyhistidine tag facilitates detection of the expressed protein with
anti-His antibodies and also purification of the protein using affinity purification. After
wards KMP-11 coding region was sequenced and the recombinant protein was induced and
purified from Escherichia coli cultures. The results of the present study will increase our
knowledge about molecular cloning and expression of the L. tropica KMP-11 gene, and this
may be used as an effective target for controlling cutenous leishmaniasis.- |
doi_str_mv | 10.12816/0006470 |
format | Article |
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protozoa studded so far. This protein which is highly expressed in all stages of
the Leishmania life cycle is considered a potential candidate for a leishmaniasis vaccine
against many leishmania species. KMP-11 has been recently described in Leishmania tropica.
In the present study, the KMP-11 gene was extracted from L. tropica by PCR using two
oligonucleotide primers designed to amplify the entire coding region of this gene. Then, the
purified PCR products were successfully ligated into a high expression vector the pRSETGFP.
This expression vector provides the opportunity to clone the desired insert as a fusion
protein with a GFP and a tag, polyhistidine region. The GFP use as a carrier to improve immune
response and the polyhistidine tag facilitates detection of the expressed protein with
anti-His antibodies and also purification of the protein using affinity purification. After
wards KMP-11 coding region was sequenced and the recombinant protein was induced and
purified from Escherichia coli cultures. The results of the present study will increase our
knowledge about molecular cloning and expression of the L. tropica KMP-11 gene, and this
may be used as an effective target for controlling cutenous leishmaniasis.-</description><identifier>ISSN: 1110-0583</identifier><identifier>EISSN: 2090-2549</identifier><identifier>DOI: 10.12816/0006470</identifier><identifier>PMID: 25597146</identifier><language>eng</language><publisher>Cairo - Egypt: The Egyptian Society of Parasitology</publisher><subject>Animals ; ANTIBODIES ; Cloning, Molecular ; Gene Expression Regulation - physiology ; IMMUNITY ; LEISHMANIA ; LEISHMANIA TROPICA ; Leishmania tropica - genetics ; Leishmaniasis ; Membrane Proteins - genetics ; Membrane Proteins - metabolism ; Molecular aspects ; Molecular cloning ; PROTEINS ; Protozoan Proteins - genetics ; Protozoan Proteins - metabolism ; الأجسام المضادة ; الاستنساخ الجزيئي ; البروتينات ; الليثسمانيا الإستوائية ; الليشمانيا ; المناعة ; داء الليشمانيات</subject><ispartof>Journal of the Egyptian Society of Parasitology, 2014-08, Vol.44 (2), p.321-328</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a242t-29e2c9640cfd2cca243dfa3353552d94e302d3792e338606af4edd41a7b67f43</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttps://static.almanhal.com/covers/titl/53676/cover-lg.jpg</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25597146$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Abbady , Abdul Qader A</creatorcontrib><creatorcontrib>Meriee , Mouayad</creatorcontrib><creatorcontrib>Soukkarieh , Chadi</creatorcontrib><title>Molecular Cloning and Expression of the Leishmania Tropica Kmp-11 Gene</title><title>Journal of the Egyptian Society of Parasitology</title><addtitle>J Egypt Soc Parasitol</addtitle><description>Kinetoplastid membrane protein-11 (KMP-11) is a small protein of 11 kDa present in all kinetoplastid
protozoa studded so far. This protein which is highly expressed in all stages of
the Leishmania life cycle is considered a potential candidate for a leishmaniasis vaccine
against many leishmania species. KMP-11 has been recently described in Leishmania tropica.
In the present study, the KMP-11 gene was extracted from L. tropica by PCR using two
oligonucleotide primers designed to amplify the entire coding region of this gene. Then, the
purified PCR products were successfully ligated into a high expression vector the pRSETGFP.
This expression vector provides the opportunity to clone the desired insert as a fusion
protein with a GFP and a tag, polyhistidine region. The GFP use as a carrier to improve immune
response and the polyhistidine tag facilitates detection of the expressed protein with
anti-His antibodies and also purification of the protein using affinity purification. After
wards KMP-11 coding region was sequenced and the recombinant protein was induced and
purified from Escherichia coli cultures. The results of the present study will increase our
knowledge about molecular cloning and expression of the L. tropica KMP-11 gene, and this
may be used as an effective target for controlling cutenous leishmaniasis.-</description><subject>Animals</subject><subject>ANTIBODIES</subject><subject>Cloning, Molecular</subject><subject>Gene Expression Regulation - physiology</subject><subject>IMMUNITY</subject><subject>LEISHMANIA</subject><subject>LEISHMANIA TROPICA</subject><subject>Leishmania tropica - genetics</subject><subject>Leishmaniasis</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - metabolism</subject><subject>Molecular aspects</subject><subject>Molecular cloning</subject><subject>PROTEINS</subject><subject>Protozoan Proteins - genetics</subject><subject>Protozoan Proteins - metabolism</subject><subject>الأجسام المضادة</subject><subject>الاستنساخ الجزيئي</subject><subject>البروتينات</subject><subject>الليثسمانيا الإستوائية</subject><subject>الليشمانيا</subject><subject>المناعة</subject><subject>داء الليشمانيات</subject><issn>1110-0583</issn><issn>2090-2549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1LAzEQhoMottSCf0DJ0ctqvrc5SmmrWPHS-5ImE7uS3aybLui_N9haD8PAOw8vw4PQNSX3lM2oeiCEKFGSMzRmRJOCSaHP0ZhSSgoiZ3yEpil9ZIgqLvJcohGTUpdUqDFavsYAdgimx_MQ27p9x6Z1ePHV9ZBSHVscPd7vAK-hTrvGtLXBmz52tTX4pekKSvEKWrhCF96EBNPjnqDNcrGZPxXrt9Xz_HFdGCbYvmAamNVKEOsdszaH3HnDueRSMqcFcMIcLzUDzmeKKOMFOCeoKbeq9IJP0N2htuvj5wBpXzV1shCCaSEOqaJKMkF1Sfg_avuYUg--6vq6Mf13RUn16606esvo7bF12DbgTuCfpQzcHADIOXhzIgRj-dv_uwnZ0M6EEyC5KhX_AVxOeHk</recordid><startdate>20140801</startdate><enddate>20140801</enddate><creator>Abbady , Abdul Qader A</creator><creator>Meriee , Mouayad</creator><creator>Soukkarieh , Chadi</creator><general>The Egyptian Society of Parasitology</general><scope>~6Z</scope><scope>ADJCN</scope><scope>AHFXO</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20140801</creationdate><title>Molecular Cloning and Expression of the Leishmania Tropica Kmp-11 Gene</title><author>Abbady , Abdul Qader A ; Meriee , Mouayad ; Soukkarieh , Chadi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a242t-29e2c9640cfd2cca243dfa3353552d94e302d3792e338606af4edd41a7b67f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>ANTIBODIES</topic><topic>Cloning, Molecular</topic><topic>Gene Expression Regulation - physiology</topic><topic>IMMUNITY</topic><topic>LEISHMANIA</topic><topic>LEISHMANIA TROPICA</topic><topic>Leishmania tropica - genetics</topic><topic>Leishmaniasis</topic><topic>Membrane Proteins - genetics</topic><topic>Membrane Proteins - metabolism</topic><topic>Molecular aspects</topic><topic>Molecular cloning</topic><topic>PROTEINS</topic><topic>Protozoan Proteins - genetics</topic><topic>Protozoan Proteins - metabolism</topic><topic>الأجسام المضادة</topic><topic>الاستنساخ الجزيئي</topic><topic>البروتينات</topic><topic>الليثسمانيا الإستوائية</topic><topic>الليشمانيا</topic><topic>المناعة</topic><topic>داء الليشمانيات</topic><toplevel>online_resources</toplevel><creatorcontrib>Abbady , Abdul Qader A</creatorcontrib><creatorcontrib>Meriee , Mouayad</creatorcontrib><creatorcontrib>Soukkarieh , Chadi</creatorcontrib><collection>Al Manhal All Journals Collection</collection><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the Egyptian Society of Parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abbady , Abdul Qader A</au><au>Meriee , Mouayad</au><au>Soukkarieh , Chadi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular Cloning and Expression of the Leishmania Tropica Kmp-11 Gene</atitle><jtitle>Journal of the Egyptian Society of Parasitology</jtitle><addtitle>J Egypt Soc Parasitol</addtitle><date>2014-08-01</date><risdate>2014</risdate><volume>44</volume><issue>2</issue><spage>321</spage><epage>328</epage><pages>321-328</pages><issn>1110-0583</issn><eissn>2090-2549</eissn><abstract>Kinetoplastid membrane protein-11 (KMP-11) is a small protein of 11 kDa present in all kinetoplastid
protozoa studded so far. This protein which is highly expressed in all stages of
the Leishmania life cycle is considered a potential candidate for a leishmaniasis vaccine
against many leishmania species. KMP-11 has been recently described in Leishmania tropica.
In the present study, the KMP-11 gene was extracted from L. tropica by PCR using two
oligonucleotide primers designed to amplify the entire coding region of this gene. Then, the
purified PCR products were successfully ligated into a high expression vector the pRSETGFP.
This expression vector provides the opportunity to clone the desired insert as a fusion
protein with a GFP and a tag, polyhistidine region. The GFP use as a carrier to improve immune
response and the polyhistidine tag facilitates detection of the expressed protein with
anti-His antibodies and also purification of the protein using affinity purification. After
wards KMP-11 coding region was sequenced and the recombinant protein was induced and
purified from Escherichia coli cultures. The results of the present study will increase our
knowledge about molecular cloning and expression of the L. tropica KMP-11 gene, and this
may be used as an effective target for controlling cutenous leishmaniasis.-</abstract><cop>Cairo - Egypt</cop><pub>The Egyptian Society of Parasitology</pub><pmid>25597146</pmid><doi>10.12816/0006470</doi><tpages>8</tpages></addata></record> |
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source | MEDLINE; Alma/SFX Local Collection |
subjects | Animals ANTIBODIES Cloning, Molecular Gene Expression Regulation - physiology IMMUNITY LEISHMANIA LEISHMANIA TROPICA Leishmania tropica - genetics Leishmaniasis Membrane Proteins - genetics Membrane Proteins - metabolism Molecular aspects Molecular cloning PROTEINS Protozoan Proteins - genetics Protozoan Proteins - metabolism الأجسام المضادة الاستنساخ الجزيئي البروتينات الليثسمانيا الإستوائية الليشمانيا المناعة داء الليشمانيات |
title | Molecular Cloning and Expression of the Leishmania Tropica Kmp-11 Gene |
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