TY - JOUR
T1 - A highly sensitive “turn-on” fluorescent probe with an aggregation-induced emission characteristic for quantitative detection of γ-globulin
AU - Liu, Pai
AU - Chen, Didi
AU - Wang, Yuanhang
AU - Tang, Xiaoying
AU - Li, Hanjun
AU - Shi, Jianbing
AU - Tong, Bin
AU - Dong, Yuping
N1 - Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2017/6/15
Y1 - 2017/6/15
N2 - 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 7.89−300 μg/mL. The detection limit of γ-globulins was determined to be 7.89 μg/mL. The fluorescence response time of TABD-Py-PF6 for detecting γ-globulins was very short (below 5 s), 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.
AB - 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 7.89−300 μg/mL. The detection limit of γ-globulins was determined to be 7.89 μg/mL. The fluorescence response time of TABD-Py-PF6 for detecting γ-globulins was very short (below 5 s), 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.
KW - Aggregation-induced emission
KW - Buta-1,3-diene derivative
KW - In-situ detection
KW - Pyridine salt
KW - γ-Globulin
UR - http://www.scopus.com/inward/record.url?scp=85014422627&partnerID=8YFLogxK
U2 - 10.1016/j.bios.2016.10.064
DO - 10.1016/j.bios.2016.10.064
M3 - Article
C2 - 27838204
AN - SCOPUS:85014422627
SN - 0956-5663
VL - 92
SP - 536
EP - 541
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
ER -