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NaLi-H1: A universal synthetic library of humanized nanobodies providing highly functional antibodies and intrabodies
In vitro selection of antibodies allows to obtain highly functional binders, rapidly and at lower cost. Here, we describe the first fully synthetic phage display library of humanized llama single domain antibody (NaLi-H1: Nanobody Library Humanized 1). Based on a humanized synthetic single domain an...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985285/ https://www.ncbi.nlm.nih.gov/pubmed/27434673 http://dx.doi.org/10.7554/eLife.16228 |
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author | Moutel, Sandrine Bery, Nicolas Bernard, Virginie Keller, Laura Lemesre, Emilie de Marco, Ario Ligat, Laetitia Rain, Jean-Christophe Favre, Gilles Olichon, Aurélien Perez, Franck |
author_facet | Moutel, Sandrine Bery, Nicolas Bernard, Virginie Keller, Laura Lemesre, Emilie de Marco, Ario Ligat, Laetitia Rain, Jean-Christophe Favre, Gilles Olichon, Aurélien Perez, Franck |
author_sort | Moutel, Sandrine |
collection | PubMed |
description | In vitro selection of antibodies allows to obtain highly functional binders, rapidly and at lower cost. Here, we describe the first fully synthetic phage display library of humanized llama single domain antibody (NaLi-H1: Nanobody Library Humanized 1). Based on a humanized synthetic single domain antibody (hs2dAb) scaffold optimized for intracellular stability, the highly diverse library provides high affinity binders without animal immunization. NaLi-H1 was screened following several selection schemes against various targets (Fluorescent proteins, actin, tubulin, p53, HP1). Conformation antibodies against active RHO GTPase were also obtained. Selected hs2dAb were used in various immunoassays and were often found to be functional intrabodies, enabling tracking or inhibition of endogenous targets. Functionalization of intrabodies allowed specific protein knockdown in living cells. Finally, direct selection against the surface of tumor cells produced hs2dAb directed against tumor-specific antigens further highlighting the potential use of this library for therapeutic applications. DOI: http://dx.doi.org/10.7554/eLife.16228.001 |
format | Online Article Text |
id | pubmed-4985285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49852852016-08-23 NaLi-H1: A universal synthetic library of humanized nanobodies providing highly functional antibodies and intrabodies Moutel, Sandrine Bery, Nicolas Bernard, Virginie Keller, Laura Lemesre, Emilie de Marco, Ario Ligat, Laetitia Rain, Jean-Christophe Favre, Gilles Olichon, Aurélien Perez, Franck eLife Cell Biology In vitro selection of antibodies allows to obtain highly functional binders, rapidly and at lower cost. Here, we describe the first fully synthetic phage display library of humanized llama single domain antibody (NaLi-H1: Nanobody Library Humanized 1). Based on a humanized synthetic single domain antibody (hs2dAb) scaffold optimized for intracellular stability, the highly diverse library provides high affinity binders without animal immunization. NaLi-H1 was screened following several selection schemes against various targets (Fluorescent proteins, actin, tubulin, p53, HP1). Conformation antibodies against active RHO GTPase were also obtained. Selected hs2dAb were used in various immunoassays and were often found to be functional intrabodies, enabling tracking or inhibition of endogenous targets. Functionalization of intrabodies allowed specific protein knockdown in living cells. Finally, direct selection against the surface of tumor cells produced hs2dAb directed against tumor-specific antigens further highlighting the potential use of this library for therapeutic applications. DOI: http://dx.doi.org/10.7554/eLife.16228.001 eLife Sciences Publications, Ltd 2016-07-19 /pmc/articles/PMC4985285/ /pubmed/27434673 http://dx.doi.org/10.7554/eLife.16228 Text en © 2016, Moutel et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Moutel, Sandrine Bery, Nicolas Bernard, Virginie Keller, Laura Lemesre, Emilie de Marco, Ario Ligat, Laetitia Rain, Jean-Christophe Favre, Gilles Olichon, Aurélien Perez, Franck NaLi-H1: A universal synthetic library of humanized nanobodies providing highly functional antibodies and intrabodies |
title | NaLi-H1: A universal synthetic library of humanized nanobodies providing highly functional antibodies and intrabodies |
title_full | NaLi-H1: A universal synthetic library of humanized nanobodies providing highly functional antibodies and intrabodies |
title_fullStr | NaLi-H1: A universal synthetic library of humanized nanobodies providing highly functional antibodies and intrabodies |
title_full_unstemmed | NaLi-H1: A universal synthetic library of humanized nanobodies providing highly functional antibodies and intrabodies |
title_short | NaLi-H1: A universal synthetic library of humanized nanobodies providing highly functional antibodies and intrabodies |
title_sort | nali-h1: a universal synthetic library of humanized nanobodies providing highly functional antibodies and intrabodies |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4985285/ https://www.ncbi.nlm.nih.gov/pubmed/27434673 http://dx.doi.org/10.7554/eLife.16228 |
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