mRuby, a bright monomeric red fluorescent protein for labeling of subcellular structures


Kredel, Simone, Oswald, Franz, Nienhaus, Karin, Deuschle, Karen, Röcke, Carlheinz, Wolff, Michael, Heilker, Ralf, Nienhaus, G. Ulrich and Wiedenmann, Jörg (2009) mRuby, a bright monomeric red fluorescent protein for labeling of subcellular structures. PLoS ONE, 4, (2), e4391. (doi:10.1371/journal.pone.0004391).

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Description/Abstract

A monomeric variant of the red fluorescent protein eqFP611, mRuby, is described. With excitation and emission maxima at 558 nm and 605 nm, respectively, and a large Stokes shift of 47 nm, mRuby appears particularly useful for imaging applications. The protein shows an exceptional resistance to denaturation at pH extremes. Moreover, mRuby is about ten-fold brighter compared to EGFP when being targeted to the endoplasmic reticulum. The engineering process of eqFP611 revealed that the C-terminal tail of the protein acts as a natural peroxisomal targeting signal (PTS). Using an mRuby variant carrying the eqFP611-PTS, we discovered that ordered inheritance of peroxisomes is widespread during mitosis of different mammalian cell types. The ordered partitioning is realized by the formation of peroxisome clusters around the poles of the mitotic spindle and ensures that equal numbers of the organelle are inherited by the daughter cells. The unique spectral properties make mRuby the marker of choice for a multitude of cell biological applications. Moreover, the use of mRuby has allowed novel insights in the biology of organelles responsible for severe human diseases.

Item Type: Article
ISSNs: 1932-6203 (print)
Related URLs:
Subjects: Q Science > QH Natural history > QH301 Biology
Divisions: University Structure - Pre August 2011 > School of Ocean & Earth Science (SOC/SOES)
ePrint ID: 65392
Date Deposited: 05 Feb 2009
Last Modified: 27 Mar 2014 18:46
URI: http://eprints.soton.ac.uk/id/eprint/65392

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