Activity-Based Near-Infrared Fluorogenic Probe for Enabling in Vitro and in Vivo Profiling of Neutrophil Elastase

化学 体内 荧光团 中性粒细胞弹性蛋白酶 体外 检出限 蛋白酵素 丝氨酸蛋白酶 荧光 硼酸 生物物理学 蛋白酶 生物化学 炎症 免疫学 组合化学 色谱法 物理 生物技术 生物 量子力学
作者
Shiyu Liu,Hao Xiong,Rongrong Li,Wen‐Chao Yang,Guang‐Fu Yang
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:91 (6): 3877-3884 被引量:50
标识
DOI:10.1021/acs.analchem.8b04455
摘要

Neutrophil elastase (NE), a typical hematopoietic serine protease, has significant roles in inflammatory and immune responses, and thus is highly associated with various diseases such as acute lung injury (ALI) and lung cancer. Rapid and accurate measurement of NE activity in biological systems is particularly important for understanding the role of NE in inflammatory diseases, as well as clinical diagnosis. However, the specific detection and noninvasive imaging of NE in vivo remains a challenge. To address this issue, a small-molecule substrate based near-infrared fluorogenic probe (NEP) for NE was constructed via incorporating pentafluoroethyl as the recognition group with a hemicyanine dye-based fluorophore. This initially quenched probe possesses more than 25-fold red fluorescence enhancement upon the catalysis of human NE, and the detection limit is about 29.6 ng/mL. In addition, the high specificity and the long emission wavelength (λemmax = 700 nm) of NEP allowed the direct monitoring of NE-trafficking, exogenous NE uptake, and endogenous NE upregulation at the cellular level. Moreover, the successful spatiotemporal imaging of NE in ALI model mice also made it a promising new tool in clinical diagnosis for ALI and other lung diseases.
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