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Fabrication of molecular tension probes

A unique bioluminescent imaging probe is introduced for illuminating molecular tension appended by protein–protein interactions (PPIs) of interest. A full-length luciferase is sandwiched between two proteins of interest via minimal flexible linkers. The ligand-activated PPIs append intramolecular te...

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Detalles Bibliográficos
Autores principales: Kim, Sung Bae, Fujii, Rika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821449/
https://www.ncbi.nlm.nih.gov/pubmed/27222821
http://dx.doi.org/10.1016/j.mex.2016.03.008
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author Kim, Sung Bae
Fujii, Rika
author_facet Kim, Sung Bae
Fujii, Rika
author_sort Kim, Sung Bae
collection PubMed
description A unique bioluminescent imaging probe is introduced for illuminating molecular tension appended by protein–protein interactions (PPIs) of interest. A full-length luciferase is sandwiched between two proteins of interest via minimal flexible linkers. The ligand-activated PPIs append intramolecular tension to the sandwiched luciferase, boosting or dropping the enzymatic activity in a quantitative manner. This method guides construction of a new lineage of bioassays for determining molecular tension appended by ligand-activated PPIs. The summary of the method is: • Molecular tension appended by protein–protein interactions (PPI) is visualized with a luciferase. • Estrogen activities are quantitatively illuminated with the molecular tension probes. • Full-length Renilla luciferase enhances the optical intensities after bending by PPI.
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spelling pubmed-48214492016-05-24 Fabrication of molecular tension probes Kim, Sung Bae Fujii, Rika MethodsX Biochemistry, Genetics and Molecular Biology A unique bioluminescent imaging probe is introduced for illuminating molecular tension appended by protein–protein interactions (PPIs) of interest. A full-length luciferase is sandwiched between two proteins of interest via minimal flexible linkers. The ligand-activated PPIs append intramolecular tension to the sandwiched luciferase, boosting or dropping the enzymatic activity in a quantitative manner. This method guides construction of a new lineage of bioassays for determining molecular tension appended by ligand-activated PPIs. The summary of the method is: • Molecular tension appended by protein–protein interactions (PPI) is visualized with a luciferase. • Estrogen activities are quantitatively illuminated with the molecular tension probes. • Full-length Renilla luciferase enhances the optical intensities after bending by PPI. Elsevier 2016-03-18 /pmc/articles/PMC4821449/ /pubmed/27222821 http://dx.doi.org/10.1016/j.mex.2016.03.008 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Biochemistry, Genetics and Molecular Biology
Kim, Sung Bae
Fujii, Rika
Fabrication of molecular tension probes
title Fabrication of molecular tension probes
title_full Fabrication of molecular tension probes
title_fullStr Fabrication of molecular tension probes
title_full_unstemmed Fabrication of molecular tension probes
title_short Fabrication of molecular tension probes
title_sort fabrication of molecular tension probes
topic Biochemistry, Genetics and Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821449/
https://www.ncbi.nlm.nih.gov/pubmed/27222821
http://dx.doi.org/10.1016/j.mex.2016.03.008
work_keys_str_mv AT kimsungbae fabricationofmoleculartensionprobes
AT fujiirika fabricationofmoleculartensionprobes