合理设计
荧光
高通量筛选
生物化学
微生物
化学
水解酶
小肠
糖尿病
生物
酶
细菌
内分泌学
遗传学
物理
量子力学
作者
Wei Cai,Wenbo Sun,Jiayue Wang,Xiaokui Huo,Xudong Cao,Xiangge Tian,Xiaochi Ma,Lei Feng
标识
DOI:10.1016/j.snb.2023.134878
摘要
α-Glucosidase (α-GLC) as a key hydrolase plays an important role in controlling blood glucose. In this work, we developed a α-GLC-activated near-infrared fluorescent probe HCBG by rational design and chemical molecular docking. HCBG showed excellent selectivity and sensitivity toward α-GLC in complex bio-samples. With the advantage of its good cell permeability realizing the in situ real-time imaging of α-GLC in intestinal microorganism, living cells, and animals. Importantly, 5 human fungi with high α-GLC expression were successfully screened out and imaged from 57 human intestinal fungi. More importantly, among them, the intestine colonization of M2204 and PB005A in animal can significantly influence glucose metabolism in intestine further increase the blood glucose levels to 9.1 mmol/L. Finally, using the high-throughput screening system established by HCBG, 1-Deoxynojirimycin as a natural inhibitor of α-GLC was isolated and identified, and IC50 is 1.58 μM. In summary, this study provides a novel fluorescence visualization tool for discovering and exploring the biological functions of diabetes-related gut microbiota and the high-throughput screening approach for α-GLC inhibitor.
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