Pan Qiuyuan, Xie Feiran, Hu Honghua, Huang Luyi, Zhou Yanzhi, Jing Jun, Song Li, Li Lin, Xiao Peihong
Department of Laboratory Medicine and Sichuan Provincial Key Laboratory for Human Disease Gene Study, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu 610041, China.
Key Laboratory of Molecular Biology for Infectious Diseases (Ministry of Education), Institute for Viral Hepatitis, Department of Infectious Diseases, The Second Affiliated Hospital, Chongqing Medical University, Chongqing 400010, China.
Anal Chem. 2025 Jun 3;97(21):11269-11278. doi: 10.1021/acs.analchem.5c01359. Epub 2025 May 5.
The current clinical diagnostic criteria for acute kidney injury (AKI) are based on the evaluation of changes in serum biomarkers (sCr, BUN) and urine output, which are insensitive and typically do not show significant differences until the middle to late stages, thereby hindering the time diagnosis of AKI. Herein, we report an N-acetyl-β-d-glucosaminidase (NAG)-activatable glow-type chemiluminescent probe (CL-NAG) for sensitive detection of urinary NAG and early diagnosis of AKI. CL-NAG was designed and synthesized by incorporating N-acetyl-β-d-glucosamine into the phenoxy-dioxetane scaffolds through a self-immolative linker. Molecular docking calculations predicted a strong interaction between CL-NAG and the catalytic cavity of the NAG enzyme. CL-NAG exhibited high detection sensitivity (LOD = 0.042 U/L) for NAG activity, low autofluorescence interference, and an extremely high signal-to-noise ratio (1628-fold). Furthermore, using this probe, we achieved not only the imaging detection of NAG in HUVEC and HK-2 cells but also the quantitative detection of NAG activity in the urine of an AKI mouse model at different time points. Most importantly, CL-NAG successfully identified 19 positive and 149 negative samples out of 168 clinical urine specimens, proving a high consistency rate of 95.24% compared with clinical biochemical methods. This research demonstrates the sensitive urinary NAG detection ability of CL-NAG and suggests the enormous clinical application potential of CL-NAG in the early diagnosis of AKI.
目前急性肾损伤(AKI)的临床诊断标准基于对血清生物标志物(血肌酐、尿素氮)变化和尿量的评估,这些指标不敏感,通常直到中晚期才会出现显著差异,从而阻碍了AKI的早期诊断。在此,我们报道了一种可被N - 乙酰 - β - D - 氨基葡萄糖苷酶(NAG)激活的发光型化学发光探针(CL - NAG),用于灵敏检测尿NAG并早期诊断AKI。CL - NAG是通过自毁性连接子将N - 乙酰 - β - D - 氨基葡萄糖掺入苯氧基二氧杂环丁烷支架中设计合成的。分子对接计算预测CL - NAG与NAG酶的催化腔之间存在强相互作用。CL - NAG对NAG活性表现出高检测灵敏度(检测限 = 0.042 U/L)、低自发荧光干扰和极高的信噪比(1628倍)。此外,使用该探针,我们不仅实现了在人脐静脉内皮细胞(HUVEC)和人肾小管上皮细胞(HK - 2)中对NAG的成像检测,还实现了对AKI小鼠模型不同时间点尿液中NAG活性的定量检测。最重要的是,CL - NAG在168份临床尿液标本中成功鉴定出19份阳性和149份阴性样本,与临床生化方法相比,一致性率高达95.24%。本研究证明了CL - NAG对尿NAG的灵敏检测能力,并表明CL - NAG在AKI早期诊断中具有巨大的临床应用潜力。