posted on 2016-02-05, 17:37authored byAntoine Wallabregue, Dimitri Moreau, Peter Sherin, Pau Moneva Lorente, Zdeňka Jarolímová, Eric Bakker, Eric Vauthey, Jean Gruenberg, Jérôme Lacour
Late
endosomes are a major trafficking hub in the cell at the crossroads
between endocytosis, autophagy, and degradation in lysosomes. Herein
is disclosed the first small molecule allowing their selective imaging
and monitoring in the form of a diazaoxatriangulene fluorophore, 1a (hexadecyl side chain). The compound is prepared in three
steps from a simple carbenium precursor. In nanospheres, this pH-sensitive
(pKa = 7.3), photochemically stable dye
fluoresces in the red part of visible light (601 and 578 nm, acid
and basic forms, respectively) with a quantum yield between 14 and
16% and an excited-state lifetime of 7.7–7.8 ns. Importantly,
the protonated form 1a·H+ provokes a
specific staining of late endosome compartments (pH 5.0–5.5)
after 5 h of incubation with HeLa cells. Not surprisingly, this late
endosome marking depends on the intra-organelle pH, and changing the
nature of the lipophilic chain provokes a loss of selectivity. Interestingly,
fixation of the fluorophore is readily achieved with paraformaldehyde,
giving the possibility to image both live and fixed cells.