Synthesis and optical properties of tyramine-functionalized boron dipyrromethene dyes for cell bioimaging

被引:0
|
作者
Mao, Wen-Jie [1 ]
Wang, Tian-Tian [1 ,2 ]
Chen, Lin [1 ,3 ]
Zhang, Lei [1 ,2 ]
Li, Shan [1 ]
机构
[1] South China Univ Technol, Sch Biol & Biol Engn, MOE Int Joint Res Lab Synthet Biol & Med, Guangzhou 510640, Peoples R China
[2] South China Univ Technol, NMPA Key Lab Qual Control Blood Prod, Guangzhou 510640, Peoples R China
[3] Zhuhai Sanmed Biotech LTD, 266 Tongchang Rd, Zhuhai 519060, Guangdong, Peoples R China
关键词
BODIPY; Knoevenagel reaction; Tyramine signal amplification; Bioimaging; AMPLIFICATION; BODIPYS; PROBES;
D O I
10.1016/j.saa.2024.124980
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Tyramine signaling amplification (TSA) technology is generally applied in immunofluorescence, enzyme-linked immunoassays, in situ hybridization techniques, etc. Successful amplification of fluoresence signals cannot be achieved without excellent fluorescent dyes. BODIPY fluorophore is an ideal probe for cell fluorescence imaging, but pristine BODIPY cannot be direct used in the TSA system. In the paper, the new red-shifted tyramide-conjugated BODIPY (BDP-B/C/D) was synthesized via the Knoevenagel condensation reaction, which based on the tyramide-conjugated BODIPY (BDP-A). The synthesized dyes were combined with tyramine to obtain which could be used as a fluorescent substrate for enzymatic reaction of TSA. By using the selected substrate (BDP-C) in TSA, we found it to be more sensitive than the commercial dye 594 styramide for the detection of low-abundance antigen proteins.
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页数:8
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