Polyelectrolyte complex nanoparticles (PEC NPs) are synthesized
using two oppositely charged polyelectrolytes, i.e., anionic poly(sodium
4-styrene sulfonate) (PSS) and cationic poly(diallyldimethylammoniumchloride),
at molar mixing ratios (n–/n+) of ≈0.4, 0.67, 0.75, and 1.5 by applying
consecutive centrifugation to modify the optical property of PSS.
However, for n–/n+ ≈ 0.75, PEC NPs exhibit a larger blue shift and
a specific emission peak occurs at ≈278 nm for the 225 nm excitation.
The mechanism of such modification of PSS emission after complex formation
is proposed. This specific emission by PEC NPs nearly matches with
the optical absorption wavelength of globular proteins. The emission
intensity of PEC NPs is therefore quenched in the presence of globular
proteins (bovine serum albumin, human serum albumin, lysozyme, and
hemoglobin) through resonance energy transfer between the donor (PEC
NPs) and acceptor (globular proteins). The spectral overlap integral
and the variation of the separation distance from 1.8 to 2.5 nm between
the donor and acceptor confirm the resonance energy transfer. Sensing
of proteins by the PEC NPs is possible within the detection limit
of 5 nM and therefore such PEC NPs can be used as an efficient and
promising protein sensing material.