紧身衣
溶酶体
荧光
赫拉
硫化氢
内生
检出限
生物物理学
选择性
光化学
费斯特共振能量转移
组合化学
化学
生物化学
细胞
生物
催化作用
色谱法
酶
有机化学
硫黄
物理
量子力学
作者
Jinlei Yue,Yuanfang Tao,Jian Zhang,Han Wang,Nannan Wang,Weili Zhao
标识
DOI:10.1002/asia.202100041
摘要
Abstract Hydrogen sulfide (H 2 S) is recognized as an endogenous gaseous signaling agent in many biological activities. Lysosomes are the main metabolic site and play a pivotal role in cells. Herein, we designed and synthesized two new fluorescent probes BDP‐DNBS and BDP‐DNP with a BODIPY core to distinguish H 2 S. The sensing mechanism is based on the inhibition‐recovery of the photo‐induced electron transfer (PET) process. Through comparing the responsive behaviors of the two probes toward H 2 S, BDP‐DNBS showed a fast response time (60 s), low limit of detection (LOD, 51 nM), high sensitivity and selectivity. Moreover, the reaction mechanism was demonstrated by mass spectrometry and fluorescence off‐on mechanism was proved by density functional theory (DFT). Significantly, confocal fluorescence imaging indicated that BDP‐DNBS was successfully used to visualize H 2 S in lysosomes in living HeLa cells.
科研通智能强力驱动
Strongly Powered by AbleSci AI