posted on 2014-09-03, 00:00authored byCarsten Budke, Axel Dreyer, Jasmin Jaeger, Kerstin Gimpel, Thomas Berkemeier, Anna S. Bonin, Lilly Nagel, Carolin Plattner, Arthur
L. DeVries, Norbert Sewald, Thomas Koop
Experimental investigations of ice
recrystallization inhibition
(IRI) efficacy have been performed for a large number of different
substances, including natural antifreeze proteins (AFP) and antifreeze
glycoproteins (AFGP), several synthetic AFGP analogues, as well as
synthetic polymers. Here we define IRI efficacy as that concentration
at which the ice recrystallization rate is dominated by the IRI compound.
The investigated 39 compounds show IRI efficacies from about 2 mmol
L–1 for the least effective compound still showing
activity to about 1 nmol L–1, which corresponds
to the highest efficacy found for natural AFGP samples. Hence, the
assay employed allows for a quantitative comparison of IRI efficacy
over a range of at least 6 orders of magnitude, thereby enabling studies
of distinguishing effects induced by even subtle structural variations
in AFGP analogues that were synthesized. Our results show that AFGP
are by far the most effective IRI agents in our assay, and we surmise
that this particular efficacy may be due to their disaccharide moieties.
This supposition is supported by the fact that IRI efficacy is strongly
reduced for monosaccharide AFGP analogues, as well as for AFGP analogues
with acetyl-protected monosaccharide moieties.