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Issue 37, 2012
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Mapping viscosity in cells using molecular rotors

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Abstract

This article describes an emerging method for quantitative measurement and spatial imaging of microviscosity within individual domains of live cells. The method is based on fluorescence detection from small synthetic molecules termed ‘molecular rotors’, which are characterised by a strong response of fluorescence lifetimes or spectra to the viscosity of their immediate environment. Alongside this new method, two complementary techniques are discussed, which provide further insights into diffusion controlled processes on a microscopic scale in a biological environment. These are time resolved fluorescence anisotropy and imaging of short-lived excited state of molecular oxygen, termed ‘singlet oxygen’. It is possible to utilise all three approaches for the quantitative determination of viscosity in individual organelles of live cells. Finally, it is discussed how the major advantage of molecular rotor imaging, fast signal acquisition, can be used to monitor changing viscosity during dynamic biological processes within cells, such as photoinduced cell death.

Graphical abstract: Mapping viscosity in cells using molecular rotors

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Publication details

The article was received on 22 May 2012, accepted on 20 Jun 2012 and first published on 21 Jun 2012


Article type: Perspective
DOI: 10.1039/C2CP41674C
Citation: Phys. Chem. Chem. Phys., 2012,14, 12671-12686
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    Mapping viscosity in cells using molecular rotors

    M. K. Kuimova, Phys. Chem. Chem. Phys., 2012, 14, 12671
    DOI: 10.1039/C2CP41674C

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