Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: To, Tsz-Leung, Fadul, Michael J., Shu, Xiaokun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
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
_version_ 1782480785827168256
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
work_keys_str_mv AT totszleung singletoxygentripletenergytransferbasedimagingtechnologyformappingproteinproteinproximityinintactcells
AT fadulmichaelj singletoxygentripletenergytransferbasedimagingtechnologyformappingproteinproteinproximityinintactcells
AT shuxiaokun singletoxygentripletenergytransferbasedimagingtechnologyformappingproteinproteinproximityinintactcells