posted on 2015-03-18, 00:00authored byJay W. Grate, Kai-For Mo, Yongsoon Shin, Andreas Vasdekis, Marvin G. Warner, Ryan T. Kelly, Galya Orr, Dehong Hu, Karl J. Dehoff, Fred J. Brockman, Michael J. Wilkins
Methods to covalently conjugate Alexa
Fluor dyes to cellulose nanocrystals,
at limiting amounts that retain the overall structure of the nanocrystals
as model cellulose materials, were developed using two approaches.
In the first, aldehyde groups are created on the cellulose surfaces
by reaction with limiting amounts of sodium periodate, a reaction
well-known for oxidizing vicinal diols to create dialdehyde structures.
Reductive amination reactions were then applied to bind Alexa Fluor
dyes with terminal amino-groups on the linker section. In the absence
of the reductive step, dye washes out of the nanocrystal suspension,
whereas with the reductive step, a colored product is obtained with
the characteristic spectral bands of the conjugated dye. In the second
approach, Alexa Fluor dyes were modified to contain chloro-substituted
triazine ring at the end of the linker section. These modified dyes
then were reacted with cellulose nanocrystals in acetonitrile at elevated
temperature, again isolating material with the characteristic spectral
bands of the Alexa Fluor dye. Reactions with Alexa Fluor 546 are given
as detailed examples, labeling on the order of 1% of the total glucopyranose
rings of the cellulose nanocrystals at dye loadings of ca. 5 μg/mg
cellulose. Fluorescent cellulose nanocrystals were deposited in pore
network microfluidic structures (PDMS) and proof-of-principle bioimaging
experiments showed that the spatial localization of the solid cellulose
deposits could be determined, and their disappearance under the action
of Celluclast enzymes or microbes could be observed over time. In
addition, single molecule fluorescence microscopy was demonstrated
as a method to follow the disappearance of solid cellulose deposits
over time, following the decrease in the number of single blinking
dye molecules with time instead of fluorescent intensity.