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A cathepsin B (Cat B)-responsive optical nanoprobe is designed and prepared for report of HL60 differentiation into macrophage. A peptide sequence FRFK is linked to fluorescein (FITC) via the distant amino group of its lysine and N-terminated with acrylic acid (AA) to yield a molecular fluorescent probe AA-FRFK (FITC). The molecular probe is further embedded in poly(lactic-co-glycolic acid) (PLGA) to form a fluorescent nanoprobe AA-FRFK (FITC)@PLGA. The resultant optical nanoprobe is degradable by lysosomal Cat B, which is expressed in macrophages with a level of 5-10 times of that in HL60 cells. As a result, a significant decrease in fluorescence intensity is associated with the differentiation process of HL60 to macrophage and can be used as an indication of the differentiation process. The findings may pave a way toward the development of a universal in vitro labeling strategy of exogenous stem cells for report of in vivo cell differentiation by a dual-mode imaging modality involving optical imaging and magnetic resonance imaging. © 2021 European Peptide Society and John Wiley & Sons, Ltd.

Citation

Chengxing Zhang, Jingjing Meng, Yanhui Zhang, Dehua Huang, Peiyang Yan, Bo Tan, Haizhen Jiang, Zongwu Deng. FITC characterization of a cathepsin B-responsive nanoprobe for report of differentiation of HL60 cells into macrophages. Journal of peptide science : an official publication of the European Peptide Society. 2022 Mar;28(3):e3371

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PMID: 34608710

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