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Updated: Mar 12, 2026

Detection of Protein Aggregation using Fluorescence Correlation Spectroscopy
Published on: April 25, 2021
A highly sensitive "turn-on" fluorescent probe with an aggregation-induced emission characteristic for quantitative
Pai Liu1, Didi Chen2, Yuanhang Wang2
1School of Life Science, Beijing Institute of Technology, 5 South Zhongguancun Street, Beijing 100081, PR China.
Abstract:
As a novel "turn on" fluorescent probe, 4-((1Z,3Z)-1,4-bis(4-(methoxycarbonyl)phenyl)-4-(pyridin-4-yl)buta-1,3-dien-1-yl)-1-methylpyridin-1-ium hexafluorophosphate (TABD-Py-PF6) with an aggregation-induced emission characteristic was synthesized for in-situ quantitation of γ-globulins in the blood serum. It was shown that the TABD-Py-PF6 probe was highly specific for γ-globulins and that other components in the blood serum, including serum albumins, fibrinogen, glucose, urea, and cholesterol, barely interfered with the molecular interactions between TABD-Py-PF6 and γ-globulins. The high specificity of this probe enabled in-situ quantitative detection of γ-globulins without isolation of γ-globulins from the blood serum. The fluorescence intensity of TABD-Py-PF6 was linearly correlated with the concentration of γ-globulins in the ranges of 7.89-300μg/mL. The detection limit of γ-globulins was determined to be 7.89μg/mL. The fluorescence response time of TABD-Py-PF6 for detecting γ-globulins was very short (below 5s), allowing for real-time detection. The mechanism of the fluorescent turn-on behavior of the TABD-Py-PF6 probe was investigated and electrostatic interactions between TABD-Py-PF6 and γ-globulins were identified.
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