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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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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. |
format | Online Article Text |
id | pubmed-7729955 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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