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Toward Quantitative “In Vivo Biochemistry” with Fluorescence Fluctuation Spectroscopy

Quantitative description of protein dynamics and interactions in vivo with temporal and spatial resolution is a key step in dissecting molecular mechanisms in cell biology. Fluorescence fluctuation spectroscopy (FFS) has recently emerged as a powerful in vivo tool for assessing molecular concentrati...

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Detalles Bibliográficos
Autores principales: Slaughter, Brian D., Li, Rong
Formato: Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002384/
https://www.ncbi.nlm.nih.gov/pubmed/21160072
http://dx.doi.org/10.1091/mbc.E10-05-0451
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author Slaughter, Brian D.
Li, Rong
author_facet Slaughter, Brian D.
Li, Rong
author_sort Slaughter, Brian D.
collection PubMed
description Quantitative description of protein dynamics and interactions in vivo with temporal and spatial resolution is a key step in dissecting molecular mechanisms in cell biology. Fluorescence fluctuation spectroscopy (FFS) has recently emerged as a powerful in vivo tool for assessing molecular concentration and movement and formation of hetero- and homo-oligomeric complexes. This article discusses point FFS-based analysis methods that have proven useful to cell biologists, focusing on the kinds of information they provide, their pros and cons, and the basic instrumentation required. Along the way, we describe briefly a few recent examples where these analyses have helped address important biological questions.
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spelling pubmed-30023842011-03-02 Toward Quantitative “In Vivo Biochemistry” with Fluorescence Fluctuation Spectroscopy Slaughter, Brian D. Li, Rong Mol Biol Cell MBoC Technical Perspective Quantitative description of protein dynamics and interactions in vivo with temporal and spatial resolution is a key step in dissecting molecular mechanisms in cell biology. Fluorescence fluctuation spectroscopy (FFS) has recently emerged as a powerful in vivo tool for assessing molecular concentration and movement and formation of hetero- and homo-oligomeric complexes. This article discusses point FFS-based analysis methods that have proven useful to cell biologists, focusing on the kinds of information they provide, their pros and cons, and the basic instrumentation required. Along the way, we describe briefly a few recent examples where these analyses have helped address important biological questions. The American Society for Cell Biology 2010-12-15 /pmc/articles/PMC3002384/ /pubmed/21160072 http://dx.doi.org/10.1091/mbc.E10-05-0451 Text en © 2010 by The American Society for Cell Biology This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0).
spellingShingle MBoC Technical Perspective
Slaughter, Brian D.
Li, Rong
Toward Quantitative “In Vivo Biochemistry” with Fluorescence Fluctuation Spectroscopy
title Toward Quantitative “In Vivo Biochemistry” with Fluorescence Fluctuation Spectroscopy
title_full Toward Quantitative “In Vivo Biochemistry” with Fluorescence Fluctuation Spectroscopy
title_fullStr Toward Quantitative “In Vivo Biochemistry” with Fluorescence Fluctuation Spectroscopy
title_full_unstemmed Toward Quantitative “In Vivo Biochemistry” with Fluorescence Fluctuation Spectroscopy
title_short Toward Quantitative “In Vivo Biochemistry” with Fluorescence Fluctuation Spectroscopy
title_sort toward quantitative “in vivo biochemistry” with fluorescence fluctuation spectroscopy
topic MBoC Technical Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002384/
https://www.ncbi.nlm.nih.gov/pubmed/21160072
http://dx.doi.org/10.1091/mbc.E10-05-0451
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