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An improved fluorescent tag and its nanobodies for membrane protein expression, stability assay, and purification

Green fluorescent proteins (GFPs) are widely used to monitor membrane protein expression, purification, and stability. An ideal reporter should be stable itself and provide high sensitivity and yield. Here, we demonstrate that a coral (Galaxea fascicularis) thermostable GFP (TGP) is by such reasons...

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Autores principales: Cai, Hongmin, Yao, Hebang, Li, Tingting, Hutter, Cedric A. J., Li, Yanfang, Tang, Yannan, Seeger, Markus A., Li, Dianfan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729955/
https://www.ncbi.nlm.nih.gov/pubmed/33303987
http://dx.doi.org/10.1038/s42003-020-01478-z
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author Cai, Hongmin
Yao, Hebang
Li, Tingting
Hutter, Cedric A. J.
Li, Yanfang
Tang, Yannan
Seeger, Markus A.
Li, Dianfan
author_facet Cai, Hongmin
Yao, Hebang
Li, Tingting
Hutter, Cedric A. J.
Li, Yanfang
Tang, Yannan
Seeger, Markus A.
Li, Dianfan
author_sort Cai, Hongmin
collection PubMed
description Green fluorescent proteins (GFPs) are widely used to monitor membrane protein expression, purification, and stability. An ideal reporter should be stable itself and provide high sensitivity and yield. Here, we demonstrate that a coral (Galaxea fascicularis) thermostable GFP (TGP) is by such reasons an improved tag compared to the conventional jellyfish GFPs. TGP faithfully reports membrane protein stability at temperatures near 90 °C (20-min heating). By contrast, the limit for the two popular GFPs is 64 °C and 74 °C. Replacing GFPs with TGP increases yield for all four test membrane proteins in four expression systems. To establish TGP as an affinity tag for membrane protein purification, several high-affinity synthetic nanobodies (sybodies), including a non-competing pair, are generated, and the crystal structure of one complex is solved. Given these advantages, we anticipate that TGP becomes a widely used tool for membrane protein structural studies.
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spelling pubmed-77299552020-12-17 An improved fluorescent tag and its nanobodies for membrane protein expression, stability assay, and purification Cai, Hongmin Yao, Hebang Li, Tingting Hutter, Cedric A. J. Li, Yanfang Tang, Yannan Seeger, Markus A. Li, Dianfan Commun Biol Article Green fluorescent proteins (GFPs) are widely used to monitor membrane protein expression, purification, and stability. An ideal reporter should be stable itself and provide high sensitivity and yield. Here, we demonstrate that a coral (Galaxea fascicularis) thermostable GFP (TGP) is by such reasons an improved tag compared to the conventional jellyfish GFPs. TGP faithfully reports membrane protein stability at temperatures near 90 °C (20-min heating). By contrast, the limit for the two popular GFPs is 64 °C and 74 °C. Replacing GFPs with TGP increases yield for all four test membrane proteins in four expression systems. To establish TGP as an affinity tag for membrane protein purification, several high-affinity synthetic nanobodies (sybodies), including a non-competing pair, are generated, and the crystal structure of one complex is solved. Given these advantages, we anticipate that TGP becomes a widely used tool for membrane protein structural studies. Nature Publishing Group UK 2020-12-10 /pmc/articles/PMC7729955/ /pubmed/33303987 http://dx.doi.org/10.1038/s42003-020-01478-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Cai, Hongmin
Yao, Hebang
Li, Tingting
Hutter, Cedric A. J.
Li, Yanfang
Tang, Yannan
Seeger, Markus A.
Li, Dianfan
An improved fluorescent tag and its nanobodies for membrane protein expression, stability assay, and purification
title An improved fluorescent tag and its nanobodies for membrane protein expression, stability assay, and purification
title_full An improved fluorescent tag and its nanobodies for membrane protein expression, stability assay, and purification
title_fullStr An improved fluorescent tag and its nanobodies for membrane protein expression, stability assay, and purification
title_full_unstemmed An improved fluorescent tag and its nanobodies for membrane protein expression, stability assay, and purification
title_short An improved fluorescent tag and its nanobodies for membrane protein expression, stability assay, and purification
title_sort improved fluorescent tag and its nanobodies for membrane protein expression, stability assay, and purification
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729955/
https://www.ncbi.nlm.nih.gov/pubmed/33303987
http://dx.doi.org/10.1038/s42003-020-01478-z
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