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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...

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Detalles Bibliográficos
Autores principales: Zou, Yaozhong, Weis, William I., Kobilka, Brian K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
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.
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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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