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Phage Display for the Generation of Antibodies for Proteome Research, Diagnostics and Therapy
Twenty years after its development, antibody phage display using filamentous bacteriophage represents the most successful in vitro antibody selection technology. Initially, its development was encouraged by the unique possibility of directly generating recombinant human antibodies for therapy. Today...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259421/ https://www.ncbi.nlm.nih.gov/pubmed/21221060 http://dx.doi.org/10.3390/molecules16010412 |
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author | Schirrmann, Thomas Meyer, Torsten Schütte, Mark Frenzel, André Hust, Michael |
author_facet | Schirrmann, Thomas Meyer, Torsten Schütte, Mark Frenzel, André Hust, Michael |
author_sort | Schirrmann, Thomas |
collection | PubMed |
description | Twenty years after its development, antibody phage display using filamentous bacteriophage represents the most successful in vitro antibody selection technology. Initially, its development was encouraged by the unique possibility of directly generating recombinant human antibodies for therapy. Today, antibody phage display has been developed as a robust technology offering great potential for automation. Generation of monospecific binders provides a valuable tool for proteome research, leading to highly enhanced throughput and reduced costs. This review presents the phage display technology, application areas of antibodies in research, diagnostics and therapy and the use of antibody phage display for these applications. |
format | Online Article Text |
id | pubmed-6259421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62594212018-12-07 Phage Display for the Generation of Antibodies for Proteome Research, Diagnostics and Therapy Schirrmann, Thomas Meyer, Torsten Schütte, Mark Frenzel, André Hust, Michael Molecules Review Twenty years after its development, antibody phage display using filamentous bacteriophage represents the most successful in vitro antibody selection technology. Initially, its development was encouraged by the unique possibility of directly generating recombinant human antibodies for therapy. Today, antibody phage display has been developed as a robust technology offering great potential for automation. Generation of monospecific binders provides a valuable tool for proteome research, leading to highly enhanced throughput and reduced costs. This review presents the phage display technology, application areas of antibodies in research, diagnostics and therapy and the use of antibody phage display for these applications. MDPI 2011-01-10 /pmc/articles/PMC6259421/ /pubmed/21221060 http://dx.doi.org/10.3390/molecules16010412 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Schirrmann, Thomas Meyer, Torsten Schütte, Mark Frenzel, André Hust, Michael Phage Display for the Generation of Antibodies for Proteome Research, Diagnostics and Therapy |
title | Phage Display for the Generation of Antibodies for Proteome Research, Diagnostics and Therapy |
title_full | Phage Display for the Generation of Antibodies for Proteome Research, Diagnostics and Therapy |
title_fullStr | Phage Display for the Generation of Antibodies for Proteome Research, Diagnostics and Therapy |
title_full_unstemmed | Phage Display for the Generation of Antibodies for Proteome Research, Diagnostics and Therapy |
title_short | Phage Display for the Generation of Antibodies for Proteome Research, Diagnostics and Therapy |
title_sort | phage display for the generation of antibodies for proteome research, diagnostics and therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259421/ https://www.ncbi.nlm.nih.gov/pubmed/21221060 http://dx.doi.org/10.3390/molecules16010412 |
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