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The discovery of a new antibody for BRIL-fused GPCR structure determination
G-protein-coupled receptors (GPCRs)—the largest family of cell-surface membrane proteins—mediate the intracellular signal transduction of many external ligands. Thus, GPCRs have become important drug targets. X-ray crystal structures of GPCRs are very useful for structure-based drug design (SBDD). H...
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/PMC7363855/ https://www.ncbi.nlm.nih.gov/pubmed/32669569 http://dx.doi.org/10.1038/s41598-020-68355-x |
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author | Miyagi, Hikaru Asada, Hidetsugu Suzuki, Michihiko Takahashi, Yuichi Yasunaga, Mai Suno, Chiyo Iwata, So Saito, Jun-ichi |
author_facet | Miyagi, Hikaru Asada, Hidetsugu Suzuki, Michihiko Takahashi, Yuichi Yasunaga, Mai Suno, Chiyo Iwata, So Saito, Jun-ichi |
author_sort | Miyagi, Hikaru |
collection | PubMed |
description | G-protein-coupled receptors (GPCRs)—the largest family of cell-surface membrane proteins—mediate the intracellular signal transduction of many external ligands. Thus, GPCRs have become important drug targets. X-ray crystal structures of GPCRs are very useful for structure-based drug design (SBDD). Herein, we produced a new antibody (SRP2070) targeting the thermostabilised apocytochrome b562 from Escherichia coli M7W/H102I/R106L (BRIL). We found that a fragment of this antibody (SRP2070Fab) facilitated the crystallisation of the BRIL-tagged, ligand bound GPCRs, 5HT(1B) and AT(2)R. Furthermore, the electron densities of the ligands were resolved, suggesting that SPR2070Fab is versatile and adaptable for GPCR SBDD. We anticipate that this new tool will significantly accelerate structure determination of other GPCRs and the design of small molecular drugs targeting them. |
format | Online Article Text |
id | pubmed-7363855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73638552020-07-17 The discovery of a new antibody for BRIL-fused GPCR structure determination Miyagi, Hikaru Asada, Hidetsugu Suzuki, Michihiko Takahashi, Yuichi Yasunaga, Mai Suno, Chiyo Iwata, So Saito, Jun-ichi Sci Rep Article G-protein-coupled receptors (GPCRs)—the largest family of cell-surface membrane proteins—mediate the intracellular signal transduction of many external ligands. Thus, GPCRs have become important drug targets. X-ray crystal structures of GPCRs are very useful for structure-based drug design (SBDD). Herein, we produced a new antibody (SRP2070) targeting the thermostabilised apocytochrome b562 from Escherichia coli M7W/H102I/R106L (BRIL). We found that a fragment of this antibody (SRP2070Fab) facilitated the crystallisation of the BRIL-tagged, ligand bound GPCRs, 5HT(1B) and AT(2)R. Furthermore, the electron densities of the ligands were resolved, suggesting that SPR2070Fab is versatile and adaptable for GPCR SBDD. We anticipate that this new tool will significantly accelerate structure determination of other GPCRs and the design of small molecular drugs targeting them. Nature Publishing Group UK 2020-07-15 /pmc/articles/PMC7363855/ /pubmed/32669569 http://dx.doi.org/10.1038/s41598-020-68355-x 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 Miyagi, Hikaru Asada, Hidetsugu Suzuki, Michihiko Takahashi, Yuichi Yasunaga, Mai Suno, Chiyo Iwata, So Saito, Jun-ichi The discovery of a new antibody for BRIL-fused GPCR structure determination |
title | The discovery of a new antibody for BRIL-fused GPCR structure determination |
title_full | The discovery of a new antibody for BRIL-fused GPCR structure determination |
title_fullStr | The discovery of a new antibody for BRIL-fused GPCR structure determination |
title_full_unstemmed | The discovery of a new antibody for BRIL-fused GPCR structure determination |
title_short | The discovery of a new antibody for BRIL-fused GPCR structure determination |
title_sort | discovery of a new antibody for bril-fused gpcr structure determination |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7363855/ https://www.ncbi.nlm.nih.gov/pubmed/32669569 http://dx.doi.org/10.1038/s41598-020-68355-x |
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