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Singlet oxygen Triplet Energy Transfer based imaging technology for mapping protein-protein proximity in intact cells
Many cellular processes are carried out by large protein complexes that can span several tens of nanometers. Whereas Forster resonance energy transfer has a detection range of <10 nm, here we report the theoretical development and experimental demonstration of a new fluorescence imaging technolog...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091638/ https://www.ncbi.nlm.nih.gov/pubmed/24905026 http://dx.doi.org/10.1038/ncomms5072 |
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author | To, Tsz-Leung Fadul, Michael J. Shu, Xiaokun |
author_facet | To, Tsz-Leung Fadul, Michael J. Shu, Xiaokun |
author_sort | To, Tsz-Leung |
collection | PubMed |
description | Many cellular processes are carried out by large protein complexes that can span several tens of nanometers. Whereas Forster resonance energy transfer has a detection range of <10 nm, here we report the theoretical development and experimental demonstration of a new fluorescence imaging technology with a detection range of up to several tens of nanometers: singlet oxygen triplet energy transfer. We demonstrate that our method confirms the topology of a large protein complex in intact cells, which spans from the endoplasmic reticulum to the outer mitochondrial membrane and the matrix. This new method is thus suited for mapping protein proximity in large protein complexes. |
format | Online Article Text |
id | pubmed-4091638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
record_format | MEDLINE/PubMed |
spelling | pubmed-40916382014-12-06 Singlet oxygen Triplet Energy Transfer based imaging technology for mapping protein-protein proximity in intact cells To, Tsz-Leung Fadul, Michael J. Shu, Xiaokun Nat Commun Article Many cellular processes are carried out by large protein complexes that can span several tens of nanometers. Whereas Forster resonance energy transfer has a detection range of <10 nm, here we report the theoretical development and experimental demonstration of a new fluorescence imaging technology with a detection range of up to several tens of nanometers: singlet oxygen triplet energy transfer. We demonstrate that our method confirms the topology of a large protein complex in intact cells, which spans from the endoplasmic reticulum to the outer mitochondrial membrane and the matrix. This new method is thus suited for mapping protein proximity in large protein complexes. 2014-06-06 /pmc/articles/PMC4091638/ /pubmed/24905026 http://dx.doi.org/10.1038/ncomms5072 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article To, Tsz-Leung Fadul, Michael J. Shu, Xiaokun Singlet oxygen Triplet Energy Transfer based imaging technology for mapping protein-protein proximity in intact cells |
title | Singlet oxygen Triplet Energy Transfer based imaging technology for mapping protein-protein proximity in intact cells |
title_full | Singlet oxygen Triplet Energy Transfer based imaging technology for mapping protein-protein proximity in intact cells |
title_fullStr | Singlet oxygen Triplet Energy Transfer based imaging technology for mapping protein-protein proximity in intact cells |
title_full_unstemmed | Singlet oxygen Triplet Energy Transfer based imaging technology for mapping protein-protein proximity in intact cells |
title_short | Singlet oxygen Triplet Energy Transfer based imaging technology for mapping protein-protein proximity in intact cells |
title_sort | singlet oxygen triplet energy transfer based imaging technology for mapping protein-protein proximity in intact cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4091638/ https://www.ncbi.nlm.nih.gov/pubmed/24905026 http://dx.doi.org/10.1038/ncomms5072 |
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