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Methods. 2018 May 1;140-141:172-177. doi: 10.1016/j.ymeth.2017.12.001. Epub 2017 Dec 6.

Detecting protein aggregation and interaction in live cells: A guide to number and brightness.

Author information

1
Wellcome Centre Human Genetics, University of Oxford, Oxford OX3 7BN, UK.
2
Wellcome Centre Human Genetics, University of Oxford, Oxford OX3 7BN, UK; Division of Structural Biology, University of Oxford, The Henry Wellcome Building for Genomic Medicine, Headington, Oxford OX3 7BN, UK. Electronic address: spadilla@well.ox.ac.uk.

Abstract

The possibility to detect and quantify protein-protein interactions with good spatial and temporal resolutions in live cells is crucial in biology. Number and brightness is a powerful approach to detect both protein aggregation/desegregation dynamics and stoichiometry in live cells. Importantly, this technique can be applied in commercial set ups: both camera based and laser scanning microscopes. It provides pixel-by-pixel information on protein oligomeric states. If performed with two colours, the technique can retrieve the stoichiometry of the reaction under study. In this review, we discuss the strengths and weaknesses of the technique, stressing which are the correct acquisition parameters for a given microscope, the main challenges in analysis, and the limitations of the technique.

PMID:
29221925
DOI:
10.1016/j.ymeth.2017.12.001
[Indexed for MEDLINE]

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