Analysis of protein dynamics with tandem fluorescent protein timers

Fluorescent timers (FTs) are fluorescent proteins that change color with time. FTs can be used as tags to follow protein dynamics in living cells. Recently we described a novel class of FTs called tandem fluorescent protein timers (tFTs). Each tFT is a tandem fusion of two different conventional flu...

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Bibliographic Details
Main Authors: Khmelinskii, Anton (Author) , Knop, Michael (Author)
Format: Chapter/Article
Language:English
Published: 07 June 2014
In: Exocytosis and Endocytosis
Year: 2014, Pages: 195-210
Online Access:Verlag, Volltext: https://link.springer.com/protocol/10.1007/978-1-4939-0944-5_13
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Author Notes:Anton Khmelinskii, Michael Knop
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Summary:Fluorescent timers (FTs) are fluorescent proteins that change color with time. FTs can be used as tags to follow protein dynamics in living cells. Recently we described a novel class of FTs called tandem fluorescent protein timers (tFTs). Each tFT is a tandem fusion of two different conventional fluorescent proteins having distinct kinetics of fluorophore maturation. tFTs suitable for studying protein dynamics on different scales can be generated from a broad range of commonly used fluorescent proteins. Here we describe how to establish new tFTs and consider potential pitfalls. We detail a protocol for quantitative fluorescence microscopy imaging and analysis of intracellular protein dynamics with tFTs in the budding yeast Saccharomyces cerevisiae.
Item Description:Gesehen am 09.08.2017
Physical Description:Online Resource
ISBN:9781493909445