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Single Molecule Tracking for Studying Nucleocytoplasmic Transport and Intranuclear Dynamics | SpringerLink
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Microscopic imaging of single fluorescent molecules within cells provides a molecular, real-time view of physiological processes in vivo. Single fluorescent molecules produce diffraction-limited light spots in the image plane, which can be localised with a very high...
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Keywords {π}
single, article, pubmed, google, scholar, molecule, kubitscheck, privacy, cookies, content, information, publish, protocol, transport, siebrasse, molecules, microscopy, nuclear, access, cas, research, search, intranuclear, imaging, cells, fluorescence, binding, cell, data, log, journal, nucleus, tracking, nucleocytoplasmic, methods, molecular, high, precision, study, mobility, time, pore, resolution, open, grunwald, biol, press, springer, site, optional,
Topics {βοΈ}
wide-field fluorescence imaging single-molecule fluorescence microscopy nonlinear structured-illumination microscopy narrow-field epifluorescence microscopy single fluorescent molecules single-molecule tracking single molecule tracking privacy choices/manage cookies high-speed imaging study intranuclear protein single molecule level single-photon microscopy high time resolution real-time view theoretically unlimited resolution high localisation precision european economic area brownian motion characterised bimolecular interaction events nuclear pore complex nuclear pore complexes nuclear protein import intranuclear binding kinetics journal finder publish conditions privacy policy fluorescence microscopy accepting optional cookies studying nucleocytoplasmic transport highly dynamic processes eukaryotic cell nuclei chapter log single molecules protocol siebrasse ribonucleoprotein particle mobility main content log check access ethics access binding site distribution humana press intranuclear dynamics soluble receptors protocol cite high precision journal publish privacy policy personal data permissions reprints books a information nuclear transport
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ScholarlyArticle:
headline:Single Molecule Tracking for Studying Nucleocytoplasmic Transport and Intranuclear Dynamics
pageEnd:361
pageStart:343
image:https://media.springernature.com/w153/springer-static/cover/book/978-1-60327-461-6.jpg
genre:
Springer Protocols
isPartOf:
name:The Nucleus
isbn:
978-1-60327-461-6
978-1-60327-460-9
type:Book
publisher:
name:Humana Press
logo:
url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
type:ImageObject
type:Organization
author:
name:Jan Peter Siebrasse
affiliation:
name:University of Bonn
address:
name:Institute for Physical and Theoretical Chemistry, Department of Biophysical Chemistry, University of Bonn, Bonn, Germany
type:PostalAddress
type:Organization
type:Person
name:Ulrich Kubitscheck
affiliation:
name:University of Bonn
address:
name:Institute for Physical and Theoretical Chemistry, Department of Biophysical Chemistry, University of Bonn, Bonn, Germany
type:PostalAddress
type:Organization
type:Person
keywords:Single-molecule fluorescence microscopy, Single-molecule tracking, Light microscopy, Nucleocytoplasmic transport, Fluorescence labelling
description:Microscopic imaging of single fluorescent molecules within cells provides a molecular, real-time view of physiological processes in vivo. Single fluorescent molecules produce diffraction-limited light spots in the image plane, which can be localised with a very high precision. In single-molecule fluorescence microscopy (SMF) the achievable localisation precision depends only on the signal-to-noise ratio (SNR) and the stability of the optical setup. Typically values between 20 and 40nm can be achieved. Highly dynamic processes and Brownian motion characterised by diffusion coefficients <20ΞΌm2/sec can be followed by high-speed imaging, hence the method is an ideal tool to study intranuclear protein or ribonucleoprotein particle mobility. In contrast to conventional techniques, different forms of mobility in a heterogeneous system may well be distinguished from each other. Furthermore, specific binding and bimolecular interaction events can be followed at the single molecule level. A prominent example of an application is the study of nucleocytoplasmic transport one molecule at a time. In this case, the high localisation precision allows to analyse the binding site distribution of single molecules at the nuclear pore complex, and the high time resolution allows determination of the binding duration of soluble receptors and transport substrates.
datePublished:2008
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Book:
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isbn:
978-1-60327-461-6
978-1-60327-460-9
Organization:
name:Humana Press
logo:
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name:University of Bonn
address:
name:Institute for Physical and Theoretical Chemistry, Department of Biophysical Chemistry, University of Bonn, Bonn, Germany
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Person:
name:Jan Peter Siebrasse
affiliation:
name:University of Bonn
address:
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type:PostalAddress
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name:Ulrich Kubitscheck
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name:University of Bonn
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name:Institute for Physical and Theoretical Chemistry, Department of Biophysical Chemistry, University of Bonn, Bonn, Germany
type:PostalAddress
type:Organization
PostalAddress:
name:Institute for Physical and Theoretical Chemistry, Department of Biophysical Chemistry, University of Bonn, Bonn, Germany
name:Institute for Physical and Theoretical Chemistry, Department of Biophysical Chemistry, University of Bonn, Bonn, Germany
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