化学
荧光
癌细胞
淋巴瘤
程序性细胞死亡
细胞凋亡
计算生物学
细胞生物学
癌症
生物化学
癌症研究
分子生物学
病理
遗传学
生物
医学
量子力学
物理
作者
Tingting Liu,Gaopan Dong,Feng Xu,Bo Han,Hao Fang,Yun Huang,Yubin Zhou,Lüpei Du,Minyong Li
标识
DOI:10.1021/acs.analchem.8b05853
摘要
B-cell-lymphoma-2-gene (Bcl-2) family proteins play a central role in regulating programmed cell death. In cancer, antiapoptotic Bcl-2 proteins, such as Bcl-2 and Mcl-1, are overexpressed. However, there are few developed labeling techniques for tracing the dynamic processes of Bcl-2. To study the physiological process of Bcl-2 protein, a novel series of small-molecule fluorescent probes (1–3) were designed and evaluated for their labeling properties. Our probes can be applied to the identification of tumor-tissue slices and the differentiation of tumor and normal tissues effectively, a feature that renders these probes compatible with future cancer diagnosis in clinical practice.
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