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Fast-dissociating but highly specific antibodies are novel tools in biology, especially useful for multiplex super-resolution microscopy

Fast-dissociating, highly specific monoclonal antibodies (FDSAs) are single-molecule imaging probes useful for many biological assays including consecutive, multiplexable super-resolution microscopy. We developed a screening assay to characterize the kinetics of antibody-antigen interactions using s...

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Detalles Bibliográficos
Autores principales: Miyoshi, Takushi, Friedman, Thomas B., Watanabe, Naoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8605432/
https://www.ncbi.nlm.nih.gov/pubmed/34841279
http://dx.doi.org/10.1016/j.xpro.2021.100967
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author Miyoshi, Takushi
Friedman, Thomas B.
Watanabe, Naoki
author_facet Miyoshi, Takushi
Friedman, Thomas B.
Watanabe, Naoki
author_sort Miyoshi, Takushi
collection PubMed
description Fast-dissociating, highly specific monoclonal antibodies (FDSAs) are single-molecule imaging probes useful for many biological assays including consecutive, multiplexable super-resolution microscopy. We developed a screening assay to characterize the kinetics of antibody-antigen interactions using single-molecule microscopy and established a pipeline to identify FDSAs from thousands of monoclonal candidates. Provided here are detailed protocols to prepare multi-well glass-bottom plates necessary for our assay to identify hybridoma clones secreting FDSAs. Synthesis of fluorescently labeled Fab fragments (Fab probes) from FDSAs is also described. For complete details on the use and execution of this protocol, please refer to Miyoshi et al. (2021).
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spelling pubmed-86054322021-11-26 Fast-dissociating but highly specific antibodies are novel tools in biology, especially useful for multiplex super-resolution microscopy Miyoshi, Takushi Friedman, Thomas B. Watanabe, Naoki STAR Protoc Protocol Fast-dissociating, highly specific monoclonal antibodies (FDSAs) are single-molecule imaging probes useful for many biological assays including consecutive, multiplexable super-resolution microscopy. We developed a screening assay to characterize the kinetics of antibody-antigen interactions using single-molecule microscopy and established a pipeline to identify FDSAs from thousands of monoclonal candidates. Provided here are detailed protocols to prepare multi-well glass-bottom plates necessary for our assay to identify hybridoma clones secreting FDSAs. Synthesis of fluorescently labeled Fab fragments (Fab probes) from FDSAs is also described. For complete details on the use and execution of this protocol, please refer to Miyoshi et al. (2021). Elsevier 2021-11-18 /pmc/articles/PMC8605432/ /pubmed/34841279 http://dx.doi.org/10.1016/j.xpro.2021.100967 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Miyoshi, Takushi
Friedman, Thomas B.
Watanabe, Naoki
Fast-dissociating but highly specific antibodies are novel tools in biology, especially useful for multiplex super-resolution microscopy
title Fast-dissociating but highly specific antibodies are novel tools in biology, especially useful for multiplex super-resolution microscopy
title_full Fast-dissociating but highly specific antibodies are novel tools in biology, especially useful for multiplex super-resolution microscopy
title_fullStr Fast-dissociating but highly specific antibodies are novel tools in biology, especially useful for multiplex super-resolution microscopy
title_full_unstemmed Fast-dissociating but highly specific antibodies are novel tools in biology, especially useful for multiplex super-resolution microscopy
title_short Fast-dissociating but highly specific antibodies are novel tools in biology, especially useful for multiplex super-resolution microscopy
title_sort fast-dissociating but highly specific antibodies are novel tools in biology, especially useful for multiplex super-resolution microscopy
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8605432/
https://www.ncbi.nlm.nih.gov/pubmed/34841279
http://dx.doi.org/10.1016/j.xpro.2021.100967
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