Combinatorial Strategies in Fluorescent Probe Development

被引:629
作者
Vendrell, Marc [4 ]
Zhai, Duanting [1 ,2 ]
Er, Jun Cheng [1 ,2 ,3 ]
Chang, Young-Tae [1 ,2 ,4 ]
机构
[1] Natl Univ Singapore, Dept Chem, Singapore 117543, Singapore
[2] Natl Univ Singapore, MedChem Program Life Sci, Singapore 117543, Singapore
[3] Natl Univ Singapore, Ctr Life Sci, Grad Sch Integrat Sci & Engn, Singapore 117456, Singapore
[4] ASTAR, Singapore Bioimaging Consortium, Lab Bioimaging Probe Dev, Singapore 138667, Singapore
关键词
SOLID-PHASE SYNTHESIS; IN-VITRO SELECTION; LANTHANIDE-BINDING TAGS; HIGH-THROUGHPUT SCREENS; HIGH-AFFINITY; DIFFERENTIAL RECEPTORS; QUANTITATIVE-ANALYSIS; PATTERN-RECOGNITION; PARALLEL SYNTHESIS; HYDROGEN-PEROXIDE;
D O I
10.1021/cr200355j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Studies relating to the role of combinatorial and high-throughput strategies in the development of fluorescent probes during the last five years, mainly as a result of the expansion of combinatorial chemistry on fluorescent scaffolds and the major improvements in high-throughput screenings and imaging methodologies, are discussed. A group of Lu has engineered libraries of catalytic DNA to prepare sensors for Pb2+ and Zn2+ ions. Chang and co-workers reported a diversity-oriented fluorescent library for the development of photostable near-infrared (NIR) dyes and derivatized a tricarbocyanine structure by nucleophilic substitution with 80 amines and subsequent acetylation. Chang and coworkers reported one of the first examples with a fluorescence image-based screen to discover an α-cell probe. A group also reported the high-throughput imaging screening of 320 rosamine compounds and discovered two fluorescent molecules with specific localization in the neural bodies and their projections as well as a good colocalization with commercially available neural tracers.
引用
收藏
页码:4391 / 4420
页数:30
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