557 / 2019-03-15 22:39:15
Tandem fluorescent protein timers for non-invasive relative protein lifetime measurement in plants
Tandem fluorescent protein lifetime measurement in plants
摘要录用
Hongtao Zhang / Rothamsted Research
Eric Linster / Centre for Organismal Studies, University of Heidelberg
Lucy Gannon / Rothamsted Research
Wiebke Leemhuis / Centre for Organismal Studies, University of Heidelberg
Chelsea A Rundle / Rothamsted Research
Frederica L Theodoulou / Rothamsted Research
Markus Wirtz / Centre for Organismal Studies, University of Heidelberg
Targeted protein degradation is an important and pervasive regulatory mechanism in plants, required for perception and response to the environment as well as developmental signalling. Despite the significance of this process, relatively few studies have assessed plant protein turnover in a quantitative fashion. Tandem fluorescent protein timers (tFTs) offer a powerful approach for the assessment of in vivo protein turnover in distinct subcellular compartments of single or multiple cells. A tFT is a fusion of two different fluorescent proteins with distinct fluorophore maturation kinetics, which enable protein age to be estimated from the ratio of fluorescence intensities of the two fluorescent proteins. Here, we used short-lived auxin signalling proteins and model N-end rule pathway reporters to demonstrate the utility of tFTs for studying protein turnover in living plant cells of Arabidopsis thaliana and Nicotiana benthamiana. We present transient expression of tFTs as an efficient screen for relative protein lifetime, useful for testing the effects of mutations and different genetic backgrounds on protein stability. This work demonstrates the potential for using stably expressed tFTs to study native protein dynamics with high temporal resolution in response to exogenous or endogenous stimuli.
DOI: https://doi.org/10.1104/pp.19.00051
重要日期
  • 会议日期

    06月16日

    2019

    06月21日

    2019

  • 05月01日 2019

    初稿截稿日期

  • 06月21日 2019

    注册截止日期

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