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N-Terminal T4 Lysozyme Fusion Facilitates Crystallization of a G Protein Coupled Receptor
A highly crystallizable T4 lysozyme (T4L) was fused to the N-terminus of the β(2) adrenergic receptor (β(2)AR), a G-protein coupled receptor (GPCR) for catecholamines. We demonstrate that the N-terminal fused T4L is sufficiently rigid relative to the receptor to facilitate crystallogenesis without t...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464249/ https://www.ncbi.nlm.nih.gov/pubmed/23056231 http://dx.doi.org/10.1371/journal.pone.0046039 |
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author | Zou, Yaozhong Weis, William I. Kobilka, Brian K. |
author_facet | Zou, Yaozhong Weis, William I. Kobilka, Brian K. |
author_sort | Zou, Yaozhong |
collection | PubMed |
description | A highly crystallizable T4 lysozyme (T4L) was fused to the N-terminus of the β(2) adrenergic receptor (β(2)AR), a G-protein coupled receptor (GPCR) for catecholamines. We demonstrate that the N-terminal fused T4L is sufficiently rigid relative to the receptor to facilitate crystallogenesis without thermostabilizing mutations or the use of a stabilizing antibody, G protein, or protein fused to the 3rd intracellular loop. This approach adds to the protein engineering strategies that enable crystallographic studies of GPCRs alone or in complex with a signaling partner. |
format | Online Article Text |
id | pubmed-3464249 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34642492012-10-10 N-Terminal T4 Lysozyme Fusion Facilitates Crystallization of a G Protein Coupled Receptor Zou, Yaozhong Weis, William I. Kobilka, Brian K. PLoS One Research Article A highly crystallizable T4 lysozyme (T4L) was fused to the N-terminus of the β(2) adrenergic receptor (β(2)AR), a G-protein coupled receptor (GPCR) for catecholamines. We demonstrate that the N-terminal fused T4L is sufficiently rigid relative to the receptor to facilitate crystallogenesis without thermostabilizing mutations or the use of a stabilizing antibody, G protein, or protein fused to the 3rd intracellular loop. This approach adds to the protein engineering strategies that enable crystallographic studies of GPCRs alone or in complex with a signaling partner. Public Library of Science 2012-10-04 /pmc/articles/PMC3464249/ /pubmed/23056231 http://dx.doi.org/10.1371/journal.pone.0046039 Text en © 2012 Zou et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Zou, Yaozhong Weis, William I. Kobilka, Brian K. N-Terminal T4 Lysozyme Fusion Facilitates Crystallization of a G Protein Coupled Receptor |
title | N-Terminal T4 Lysozyme Fusion Facilitates Crystallization of a G Protein Coupled Receptor |
title_full | N-Terminal T4 Lysozyme Fusion Facilitates Crystallization of a G Protein Coupled Receptor |
title_fullStr | N-Terminal T4 Lysozyme Fusion Facilitates Crystallization of a G Protein Coupled Receptor |
title_full_unstemmed | N-Terminal T4 Lysozyme Fusion Facilitates Crystallization of a G Protein Coupled Receptor |
title_short | N-Terminal T4 Lysozyme Fusion Facilitates Crystallization of a G Protein Coupled Receptor |
title_sort | n-terminal t4 lysozyme fusion facilitates crystallization of a g protein coupled receptor |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464249/ https://www.ncbi.nlm.nih.gov/pubmed/23056231 http://dx.doi.org/10.1371/journal.pone.0046039 |
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