Back to Search Start Over

Photo-convertible fluorescent proteins as tools for fresh insights on subcellular interactions in plants.

Authors :
GRIFFITHS, N.
JAIPARGAS, E.‐A.
WOZNY, M.R.
BARTON, K.A.
MATHUR, N.
DELFOSSE, K.
MATHUR, J.
Source :
Journal of Microscopy. Aug2016, Vol. 263 Issue 2, p148-157. 10p.
Publication Year :
2016

Abstract

Optical highlighters comprise photo-activatable, photo-switchable and photo-convertible fluorescent proteins and are relatively recent additions to the toolbox utilized for live cell imaging research. Here, we provide an overview of four photo-convertible fluorescent proteins (pcFP) that are being used in plant cell research: Eos, Kaede, Maple and Dendra2. Each of these proteins has a significant advantage over other optical highlighters since their green fluorescent nonconverted forms and red fluorescent converted forms are generally clearly visible at expression levels that do not appear to interfere with subcellular dynamics and plant development. These proteins have become increasingly useful for understanding the role of transient and sustained interactions between similar organelles. Tracking of single organelles after green-to-red conversion has provided novel insights on plastids and their stroma-filled extensions and on the formation of mega-mitochondria. Similarly colour recovery after photo-conversion has permitted the estimation of nuclear endo-reduplication events and is being developed further to image protein trafficking within the lumen of the endoplasmic reticulum. We have also applied photo-convertible proteins to create colour-differentiation between similar cell types to follow their development. Both the green and red fluorescent forms of these proteins are compatible with other commonly used single coloured FPs. This has allowed us to develop simultaneous visualization schemes for up to five types of organelles and investigate organelle interactivity. The advantages and caveats associated with the use of photo-convertible fluorescent proteins are discussed. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00222720
Volume :
263
Issue :
2
Database :
Academic Search Index
Journal :
Journal of Microscopy
Publication Type :
Academic Journal
Accession number :
116790971
Full Text :
https://doi.org/10.1111/jmi.12383