posted on 2021-09-15, 18:06authored byYu Nakagawa, Shintaro Kakihara, Kazue Tsuzuki, Makoto Ojika, Yasuhiro Igarashi, Yukishige Ito
Pradimicin A (PRM-A) and related
compounds constitute an exceptional
family of natural pigments that show Ca2+-dependent recognition
of d-mannose (Man). Although these compounds hold great promise
as research tools in glycobiology, their practical application has
been severely limited by their inherent tendency to form water-insoluble
aggregates. Here, we demonstrate that the 2-hydroxyethylamide derivative
(PRM-EA) of PRM-A shows little aggregation in neutral aqueous media
and retains binding specificity for Man. We also show that PRM-EA
stains glycoproteins in dot blot assays, whereas PRM-A fails to do
so, owing to severe aggregation. Significantly, PRM-EA is sensitive
to glycoproteins carrying high mannose-type and hybrid-type N-linked
glycans, but not to those carrying complex-type N-linked glycans.
Such staining selectivity has never been observed in conventional
dyes, suggesting that PRM-EA could serve as a unique staining agent
for the selective detection of glycoproteins with terminal Man residues.