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Updated: Sep 18, 2026

Real-time Imaging of Plant Cell Surface Dynamics with Variable-angle Epifluorescence Microscopy
Published on: December 12, 2015
A suite of fluorescent timers for visualizing protein spatiotemporal dynamics in plants
Yukihiro Nagashima1, Xin Qiao2,3, Suji Ye4
1Vegetable and Fruit Improvement Center and Department of Horticultural Sciences, Texas A&M University, College Station, TX 77843, USA.
Abstract:
Fluorescent timers (FTs), including tandem FTs (tdFTs), enable real-time visualization of precise protein localization and turnover within living cells, an essential property for elucidating protein function. In plants, application of FT has been limited largely because of the mismatch between FT maturation kinetics and the slow growth rate of plant cells. Here, we systematically evaluated multiple FT configurations to identify tdFTs optimized for plant systems. Using Arabidopsis thaliana, we tested a range of fluorescent proteins (FPs) differing in maturation times. Functional tdFT expression was confirmed in diverse organelles. Selected tdFT configurations were developed to track protein biogenesis/turnover in autoimmunity, protein transport in abiotic stress, and polarized protein translocation in determination of cell fate. When the large size of tdFT interfered with protein mobility, we developed a bipartite FT, separately tagging proteins with different FPs. This resource provides a framework for selecting FTs to dissect dynamic protein behaviors in plant cells.

