Constructing
sensor systems for rapid and selective detection of
small biomolecules such as amino acids is a major area of focus in
bioanalytical chemistry. Considering the biological relevance of arginine
and lysine, significant efforts have been directed to develop fluorescent
sensors for their detection. However, these developed sensors suffer
from certain disadvantages such as poor aqueous solubility, technically
demanding and time-consuming synthetic protocols, and more importantly,
most of them operate through single wavelength measurements, making
their performance prone to small variations in experimental conditions.
Herein, we report a ratiometric sensor that operates through lysine-
and arginine-induced dissociation of a supramolecular assembly consisting
of emissive H-aggregates of a molecular rotor dye, thioflavin-T (ThT),
on the surface of a polyanionic supramolecular host, sulfated β-cyclodextrin.
This disassembly brings out the modulation of monomer–aggregate
equilibrium in the system which acts as an ideal scheme for the ratiometric
detection of lysine and arginine in the aqueous solution. Besides
facile framework of our sensor system, it employs a commercially available
inexpensive probe molecule, ThT, which provides an added advantage
over other sensor systems that employ synthetically demanding probe
molecules. Importantly, the distinctive feature of the ratiometric
detection of arginine and lysine provides an inherent advantage of
increased accuracy in quantitative analysis. Interestingly, we have
also demonstrated that arginine displays a multiwavelength distinctive
recognition pattern which distinguishes it from lysine, using a single
supramolecular ensemble. Furthermore, our sensor system also shows
response in heterogeneous, biologically complex media of serum samples,
thus extending its possible use in real-life applications.