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Preparation of monovalent follistatin-like 3-Fc-fusion protein and evaluation of its effects on muscle mass in mice

Follistatin-like 3 (FSTL3) is an endogenous antagonist against transforming growth factor-β family ligands. Monovalent FSTL3-Fc fusion protein (mono-FSTL3-Fc) generated with knobs-into-holes technology overcomes limitations of current anti-myostatin therapies. We have developed a facile protocol for...

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Detalles Bibliográficos
Autores principales: Ozawa, Takayuki, Miyazono, Kohei, Morikawa, Masato
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455479/
https://www.ncbi.nlm.nih.gov/pubmed/34585166
http://dx.doi.org/10.1016/j.xpro.2021.100839
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author Ozawa, Takayuki
Miyazono, Kohei
Morikawa, Masato
author_facet Ozawa, Takayuki
Miyazono, Kohei
Morikawa, Masato
author_sort Ozawa, Takayuki
collection PubMed
description Follistatin-like 3 (FSTL3) is an endogenous antagonist against transforming growth factor-β family ligands. Monovalent FSTL3-Fc fusion protein (mono-FSTL3-Fc) generated with knobs-into-holes technology overcomes limitations of current anti-myostatin therapies. We have developed a facile protocol for affinity purification of the Fc-fused protein from the supernatant of HEK293T cells stably expressing the protein. This protocol is advantageous by only requiring readily accessible equipment. We further outline the steps for validation of mono-FSTL3-Fc increasing systemic muscle mass in mice after intraperitoneal administration. For complete details on the use and execution of this protocol, please refer to Ozawa et al. (2021).
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spelling pubmed-84554792021-09-27 Preparation of monovalent follistatin-like 3-Fc-fusion protein and evaluation of its effects on muscle mass in mice Ozawa, Takayuki Miyazono, Kohei Morikawa, Masato STAR Protoc Protocol Follistatin-like 3 (FSTL3) is an endogenous antagonist against transforming growth factor-β family ligands. Monovalent FSTL3-Fc fusion protein (mono-FSTL3-Fc) generated with knobs-into-holes technology overcomes limitations of current anti-myostatin therapies. We have developed a facile protocol for affinity purification of the Fc-fused protein from the supernatant of HEK293T cells stably expressing the protein. This protocol is advantageous by only requiring readily accessible equipment. We further outline the steps for validation of mono-FSTL3-Fc increasing systemic muscle mass in mice after intraperitoneal administration. For complete details on the use and execution of this protocol, please refer to Ozawa et al. (2021). Elsevier 2021-09-16 /pmc/articles/PMC8455479/ /pubmed/34585166 http://dx.doi.org/10.1016/j.xpro.2021.100839 Text en © 2021 The Author(s) 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
Ozawa, Takayuki
Miyazono, Kohei
Morikawa, Masato
Preparation of monovalent follistatin-like 3-Fc-fusion protein and evaluation of its effects on muscle mass in mice
title Preparation of monovalent follistatin-like 3-Fc-fusion protein and evaluation of its effects on muscle mass in mice
title_full Preparation of monovalent follistatin-like 3-Fc-fusion protein and evaluation of its effects on muscle mass in mice
title_fullStr Preparation of monovalent follistatin-like 3-Fc-fusion protein and evaluation of its effects on muscle mass in mice
title_full_unstemmed Preparation of monovalent follistatin-like 3-Fc-fusion protein and evaluation of its effects on muscle mass in mice
title_short Preparation of monovalent follistatin-like 3-Fc-fusion protein and evaluation of its effects on muscle mass in mice
title_sort preparation of monovalent follistatin-like 3-fc-fusion protein and evaluation of its effects on muscle mass in mice
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455479/
https://www.ncbi.nlm.nih.gov/pubmed/34585166
http://dx.doi.org/10.1016/j.xpro.2021.100839
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