Generation of functional scFv intrabody to abate the expression of CD147 surface molecule of 293A cells

Background: Expression of intracellular antibodies (intrabodies) has become a broadly applicable technology for generation of phenotypic knockouts in vivo. The method uses surface depletion of cellular membrane proteins to examine their biological function. In this study, we used this strategy to bl...

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Main Authors: Tragoolpua K., Intasai N., Kasinrerk W., Mai S., Yuan Y., Tayapiwatana C.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-39849084770&partnerID=40&md5=14a0e841282b882c246689f265927573
http://www.ncbi.nlm.nih.gov/pubmed/18226275
http://cmuir.cmu.ac.th/handle/6653943832/2494
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Institution: Chiang Mai University
Language: English
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spelling th-cmuir.6653943832-24942014-08-30T02:00:54Z Generation of functional scFv intrabody to abate the expression of CD147 surface molecule of 293A cells Tragoolpua K. Intasai N. Kasinrerk W. Mai S. Yuan Y. Tayapiwatana C. Background: Expression of intracellular antibodies (intrabodies) has become a broadly applicable technology for generation of phenotypic knockouts in vivo. The method uses surface depletion of cellular membrane proteins to examine their biological function. In this study, we used this strategy to block the transport of cell surface molecule CD147 to the cell membrane. Phage display technology was introduced to generate the functional antibody fragment to CD147, and we subsequently constructed a CD147-specific scFv that was expressed intracellularly and retained in the endoplasmic reticulum by adenoviral gene transfer. Results: The recombinant antibody fragments, Fab and scFv, of the murine monoclonal antibody (clone M6-1B9) reacted specifically to CD147 by indirect enzyme-linked immunosorbent assays (ELISA) using a recombinant CD147-BCCP as a target. This indicated that the Fab- and scFv-M6-1B9 displaying on phage surfaces were correctly folded and functionally active. We subsequently constructed a CD147-specific scFv, scFv-M6-1B9-intrabody, in 293A cells. The expression of CD147 on 293A cell surface was monitored at 36 h after transduction by flow cytometry and demonstrated remarkable reduction. Colocalization of scFv-M6-1B9 intrabody with CD147 in the ER network was depicted using a 3D deconvolution microscopy system. Conclusion: The results suggest that our approach can generate antibody fragments suitable for decreasing the expression of CD147 on 293A cells. This study represents a step toward understanding the role of the cell surface protein, CD147. © 2008 Tragoolpua et al; licensee BioMed Central Ltd. 2014-08-30T02:00:54Z 2014-08-30T02:00:54Z 2008 Article 14726750 10.1186/1472-6750-8-5 18226275 BBMIE http://www.scopus.com/inward/record.url?eid=2-s2.0-39849084770&partnerID=40&md5=14a0e841282b882c246689f265927573 http://www.ncbi.nlm.nih.gov/pubmed/18226275 http://cmuir.cmu.ac.th/handle/6653943832/2494 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Background: Expression of intracellular antibodies (intrabodies) has become a broadly applicable technology for generation of phenotypic knockouts in vivo. The method uses surface depletion of cellular membrane proteins to examine their biological function. In this study, we used this strategy to block the transport of cell surface molecule CD147 to the cell membrane. Phage display technology was introduced to generate the functional antibody fragment to CD147, and we subsequently constructed a CD147-specific scFv that was expressed intracellularly and retained in the endoplasmic reticulum by adenoviral gene transfer. Results: The recombinant antibody fragments, Fab and scFv, of the murine monoclonal antibody (clone M6-1B9) reacted specifically to CD147 by indirect enzyme-linked immunosorbent assays (ELISA) using a recombinant CD147-BCCP as a target. This indicated that the Fab- and scFv-M6-1B9 displaying on phage surfaces were correctly folded and functionally active. We subsequently constructed a CD147-specific scFv, scFv-M6-1B9-intrabody, in 293A cells. The expression of CD147 on 293A cell surface was monitored at 36 h after transduction by flow cytometry and demonstrated remarkable reduction. Colocalization of scFv-M6-1B9 intrabody with CD147 in the ER network was depicted using a 3D deconvolution microscopy system. Conclusion: The results suggest that our approach can generate antibody fragments suitable for decreasing the expression of CD147 on 293A cells. This study represents a step toward understanding the role of the cell surface protein, CD147. © 2008 Tragoolpua et al; licensee BioMed Central Ltd.
format Article
author Tragoolpua K.
Intasai N.
Kasinrerk W.
Mai S.
Yuan Y.
Tayapiwatana C.
spellingShingle Tragoolpua K.
Intasai N.
Kasinrerk W.
Mai S.
Yuan Y.
Tayapiwatana C.
Generation of functional scFv intrabody to abate the expression of CD147 surface molecule of 293A cells
author_facet Tragoolpua K.
Intasai N.
Kasinrerk W.
Mai S.
Yuan Y.
Tayapiwatana C.
author_sort Tragoolpua K.
title Generation of functional scFv intrabody to abate the expression of CD147 surface molecule of 293A cells
title_short Generation of functional scFv intrabody to abate the expression of CD147 surface molecule of 293A cells
title_full Generation of functional scFv intrabody to abate the expression of CD147 surface molecule of 293A cells
title_fullStr Generation of functional scFv intrabody to abate the expression of CD147 surface molecule of 293A cells
title_full_unstemmed Generation of functional scFv intrabody to abate the expression of CD147 surface molecule of 293A cells
title_sort generation of functional scfv intrabody to abate the expression of cd147 surface molecule of 293a cells
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-39849084770&partnerID=40&md5=14a0e841282b882c246689f265927573
http://www.ncbi.nlm.nih.gov/pubmed/18226275
http://cmuir.cmu.ac.th/handle/6653943832/2494
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