Rekombinantní fragmenty protilátek

6. CoNct usloN The aim of the thesis was to establish, in the national conditions, technology of preparation of antibody reconrbinant fragrnents and to verífo the cornplete procedure using several model monoclonal antibodies with a potential diagnostic and therapeutic use. For tfuee antibodies'...

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Main Author: Král, Vlastimil
Other Authors: Sedláček, Juraj
Format: Doctoral Thesis
Language:Czech
Published: 2008
Online Access:http://www.nusl.cz/ntk/nusl-369003
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spelling ndltd-nusl.cz-oai-invenio.nusl.cz-3690032019-05-18T03:26:20Z Rekombinantní fragmenty protilátek Recombinant Fragments of Antibodies Král, Vlastimil Sedláček, Juraj Pěknicová, Jana Hašek, Jindřich 6. CoNct usloN The aim of the thesis was to establish, in the national conditions, technology of preparation of antibody reconrbinant fragrnents and to verífo the cornplete procedure using several model monoclonal antibodies with a potential diagnostic and therapeutic use. For tfuee antibodies' mAb TU-20, M75 and MEM97, recombinant |Ťagments in various formats (scFv fragments monovalent and bivalent, i.e. diabody, and intrabody for intracellular expression) were constructed and for their heterologous expression, vectors allowing expression in E. coli (as cytoplasmic inclusions, periplasmic inclusions and in soluble form) and in Drosophila 32 cells (expression of glycosylated forms of scFv fragments into the medium) were used. In case of proteins expressed in irrsoluble form, especially scFv F|1.2.32, renaturation procedures to obtain active scFv fragments were developed and optimized. The efnect of the length of the linker -(GlyrSer).- (where x is I to 4) connecting the variable domains of the light and heavy chain on the formation of different multimeric forms of scFv rvas studied. For obtaining solell monomeric scFv fragment, the length of 20 amino acid residues tumsd out optimal. Fragnrents rvith a linker l5 residues long. formed a mixture of monomers, dimers and trimers. the proportion of rvhich rvas... 2008 info:eu-repo/semantics/doctoralThesis http://www.nusl.cz/ntk/nusl-369003 cze info:eu-repo/semantics/restrictedAccess
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language Czech
format Doctoral Thesis
sources NDLTD
description 6. CoNct usloN The aim of the thesis was to establish, in the national conditions, technology of preparation of antibody reconrbinant fragrnents and to verífo the cornplete procedure using several model monoclonal antibodies with a potential diagnostic and therapeutic use. For tfuee antibodies' mAb TU-20, M75 and MEM97, recombinant |Ťagments in various formats (scFv fragments monovalent and bivalent, i.e. diabody, and intrabody for intracellular expression) were constructed and for their heterologous expression, vectors allowing expression in E. coli (as cytoplasmic inclusions, periplasmic inclusions and in soluble form) and in Drosophila 32 cells (expression of glycosylated forms of scFv fragments into the medium) were used. In case of proteins expressed in irrsoluble form, especially scFv F|1.2.32, renaturation procedures to obtain active scFv fragments were developed and optimized. The efnect of the length of the linker -(GlyrSer).- (where x is I to 4) connecting the variable domains of the light and heavy chain on the formation of different multimeric forms of scFv rvas studied. For obtaining solell monomeric scFv fragment, the length of 20 amino acid residues tumsd out optimal. Fragnrents rvith a linker l5 residues long. formed a mixture of monomers, dimers and trimers. the proportion of rvhich rvas...
author2 Sedláček, Juraj
author_facet Sedláček, Juraj
Král, Vlastimil
author Král, Vlastimil
spellingShingle Král, Vlastimil
Rekombinantní fragmenty protilátek
author_sort Král, Vlastimil
title Rekombinantní fragmenty protilátek
title_short Rekombinantní fragmenty protilátek
title_full Rekombinantní fragmenty protilátek
title_fullStr Rekombinantní fragmenty protilátek
title_full_unstemmed Rekombinantní fragmenty protilátek
title_sort rekombinantní fragmenty protilátek
publishDate 2008
url http://www.nusl.cz/ntk/nusl-369003
work_keys_str_mv AT kralvlastimil rekombinantnifragmentyprotilatek
AT kralvlastimil recombinantfragmentsofantibodies
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