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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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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. |
format | Online Article Text |
id | pubmed-4821449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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 |