Recombinant [lambda] Bacteriophage Displaying Nanobody towards Third Domain of HER-2 Epitope Inhibits Proliferation of Breast Carcinoma SKBR-3 Cell Line
Phage display of many nanobodies via filamentous phage in combination with helper phage has been reported by many scientists. The aim of this study was to produce lambda ([lambda]) bacteriophage displaying high-affinity nanobody against HER-2 expressing breast carcinoma cells. Bacteriophage [lambda]...
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Veröffentlicht in: | Archivum Immunologiae et Therapiae Experimentalis 2013-02, Vol.61 (1), p.75-83 |
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creator | Shoae-hassani, Alireza Mortazavi-tabatabaei, Seyed Abdolreza Sharif, Shiva Madadi, Shabnam Rezaei-khaligh, Hamidreza Verdi, Javad |
description | Phage display of many nanobodies via filamentous phage in combination with helper phage has been reported by many scientists. The aim of this study was to produce lambda ([lambda]) bacteriophage displaying high-affinity nanobody against HER-2 expressing breast carcinoma cells. Bacteriophage [lambda] is a temperate phage with inherent biological safety in mammalian cells. Here we report the construction of a recombinant [lambda] phage that efficiently expresses specific nanobody towards third domain of HER-2 target on SKBR-3 and MCF-7 cell lines in vitro. We constructed recombinant [lambda] phage particles containing a mammalian expression cassette, C-Myc tagged, encoding VHH gene of camelid anti HER-2 third domain epitope using [lambda] ZAP-cytomegalic virus (CMV) vector. The SKBR-3, MCF-7 and human endometrial stem cells were treated by the nanobody displayed recombinant [lambda] phage. The cell growth inhibition assay was performed by MTT Cell Viability Assay Kit. After the fourth round of biopanning there was a significant enrichment in the phage specifically binding to the antigen. The ratio of targeted phage increased approximately 1,000-fold in the fifth round. The nanobody expressed by [lambda] ZAP-CMV-VHH phagemid cloned in [lambda] bioparticles significantly inhibited the proliferation of HER-2 positive SKBR-3 and MCF-7 cells. Recombinant bacteriophage [lambda] ZAP-CMV-VHH-cDNA could be used efficiently for construction of nanobodies to mortify HER-2 positive breast carcinoma cells as a nanomedical therapeutic.[PUBLICATION ABSTRACT] |
doi_str_mv | 10.1007/s00005-012-0206-x |
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The aim of this study was to produce lambda ([lambda]) bacteriophage displaying high-affinity nanobody against HER-2 expressing breast carcinoma cells. Bacteriophage [lambda] is a temperate phage with inherent biological safety in mammalian cells. Here we report the construction of a recombinant [lambda] phage that efficiently expresses specific nanobody towards third domain of HER-2 target on SKBR-3 and MCF-7 cell lines in vitro. We constructed recombinant [lambda] phage particles containing a mammalian expression cassette, C-Myc tagged, encoding VHH gene of camelid anti HER-2 third domain epitope using [lambda] ZAP-cytomegalic virus (CMV) vector. The SKBR-3, MCF-7 and human endometrial stem cells were treated by the nanobody displayed recombinant [lambda] phage. The cell growth inhibition assay was performed by MTT Cell Viability Assay Kit. After the fourth round of biopanning there was a significant enrichment in the phage specifically binding to the antigen. The ratio of targeted phage increased approximately 1,000-fold in the fifth round. The nanobody expressed by [lambda] ZAP-CMV-VHH phagemid cloned in [lambda] bioparticles significantly inhibited the proliferation of HER-2 positive SKBR-3 and MCF-7 cells. Recombinant bacteriophage [lambda] ZAP-CMV-VHH-cDNA could be used efficiently for construction of nanobodies to mortify HER-2 positive breast carcinoma cells as a nanomedical therapeutic.[PUBLICATION ABSTRACT]</description><identifier>ISSN: 0004-069X</identifier><identifier>EISSN: 1661-4917</identifier><identifier>DOI: 10.1007/s00005-012-0206-x</identifier><language>eng</language><publisher>Wroclaw: Springer Nature B.V</publisher><subject>Bacteria ; Cytomegalovirus</subject><ispartof>Archivum Immunologiae et Therapiae Experimentalis, 2013-02, Vol.61 (1), p.75-83</ispartof><rights>L. Hirszfeld Institute of Immunology and Experimental Therapy, Wroclaw, Poland 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Shoae-hassani, Alireza</creatorcontrib><creatorcontrib>Mortazavi-tabatabaei, Seyed Abdolreza</creatorcontrib><creatorcontrib>Sharif, Shiva</creatorcontrib><creatorcontrib>Madadi, Shabnam</creatorcontrib><creatorcontrib>Rezaei-khaligh, Hamidreza</creatorcontrib><creatorcontrib>Verdi, Javad</creatorcontrib><title>Recombinant [lambda] Bacteriophage Displaying Nanobody towards Third Domain of HER-2 Epitope Inhibits Proliferation of Breast Carcinoma SKBR-3 Cell Line</title><title>Archivum Immunologiae et Therapiae Experimentalis</title><description>Phage display of many nanobodies via filamentous phage in combination with helper phage has been reported by many scientists. The aim of this study was to produce lambda ([lambda]) bacteriophage displaying high-affinity nanobody against HER-2 expressing breast carcinoma cells. Bacteriophage [lambda] is a temperate phage with inherent biological safety in mammalian cells. Here we report the construction of a recombinant [lambda] phage that efficiently expresses specific nanobody towards third domain of HER-2 target on SKBR-3 and MCF-7 cell lines in vitro. We constructed recombinant [lambda] phage particles containing a mammalian expression cassette, C-Myc tagged, encoding VHH gene of camelid anti HER-2 third domain epitope using [lambda] ZAP-cytomegalic virus (CMV) vector. The SKBR-3, MCF-7 and human endometrial stem cells were treated by the nanobody displayed recombinant [lambda] phage. The cell growth inhibition assay was performed by MTT Cell Viability Assay Kit. After the fourth round of biopanning there was a significant enrichment in the phage specifically binding to the antigen. 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title | Recombinant [lambda] Bacteriophage Displaying Nanobody towards Third Domain of HER-2 Epitope Inhibits Proliferation of Breast Carcinoma SKBR-3 Cell Line |
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