Quantification of the Brassinosteroid Insensitive1 Receptor in Planta1[C][W]

In plants, green fluorescent protein (GFP) is routinely used to determine the subcellular location of fusion proteins. Here, we show that confocal imaging can be employed to approximate the number of GFP-labeled protein molecules present in living Arabidopsis (Arabidopsis thaliana) root cells. The t...

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Veröffentlicht in:Plant physiology (Bethesda) 2011-08, Vol.156 (4), p.1691-1700
Hauptverfasser: van Esse, G Wilma, Westphal, Adrie H, Surendran, Ramya Preethi, Albrecht, Catherine, van Veen, Boudewijn, Borst, Jan Willem, de Vries, Sacco C
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Sprache:eng
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Zusammenfassung:In plants, green fluorescent protein (GFP) is routinely used to determine the subcellular location of fusion proteins. Here, we show that confocal imaging can be employed to approximate the number of GFP-labeled protein molecules present in living Arabidopsis (Arabidopsis thaliana) root cells. The technique involves calibration with soluble GFP to provide a usable protein concentration range within the confocal volume of the microscope. As a proof of principle, we quantified the Brassinosteroid Insensitive1 (BRI1) receptor fused to GFP, under control of its own promoter. The number of BRI1-GFP molecules per root epidermal cell ranges from 22,000 in the meristem and 130,000 in the elongation zone to 80,000 in the maturation zone, indicating that up to 6-fold differences in BRI1 receptor content exist. In contrast, when taking into account differences in cell size, BRI1-GFP receptor density in the plasma membrane is kept constant at 12 receptors μm² in all cells throughout the meristem and elongation zone. Only the quiescent center and columella cells deviate from this pattern and have 5 to 6 receptors μm². Remarkably, root cell sensitivity toward brassinosteroids appears to coincide with uniform meristem receptor density.
ISSN:0032-0889
1532-2548
DOI:10.1104/pp.111.179309