Related Experiment Video
Updated: Aug 8, 2025

12:48
Construction of Cell-based Neurotransmitter Fluorescent Engineered Reporters CNiFERs for Optical Detection of Neurotransmitters In Vivo
Published on: May 12, 2016
13.3K
A modular scaffold for triggerable and tunable nitroxyl (HNO) generation with a fluorescence reporter
Laxman R Sawase1, Jishnu C V1, Suman Manna1
1Department of Chemistry, Indian Institute of Science Education and Research Pune, Pune 411 008, Maharashtra, India. harinath@iiserpune.ac.in.
Summary
New esterase-activated nitroxyl (HNO) generators allow tunable release and real-time monitoring. These tools aid understanding of cellular signaling pathways involving short-lived gaseous molecules like hydrogen sulfide (H2S).
Area of Science:
- Biochemistry
- Cell Biology
- Chemical Biology
Background:
- Nitroxyl (HNO) is a crucial short-lived signaling molecule.
- HNO enhances the sulfane sulfur pool, a cellular antioxidant reservoir, through reaction with hydrogen sulfide (H2S).
- Understanding the cross-talk between gaseous signaling molecules is vital in health and disease.
Purpose of the Study:
- To develop novel esterase-activated nitroxyl (HNO) generators.
- To enable tunable release and real-time monitoring of HNO.
- To facilitate research on the interplay of gaseous signaling molecules.
Main Methods:
- Design and synthesis of esterase-activated HNO donors.
- Characterization of HNO release kinetics.
- Real-time monitoring of HNO generation.
Main Results:
- Successfully developed esterase-activated HNO generators with tunable release properties.
- Demonstrated real-time monitoring of HNO release from these novel donors.
- Established tools for investigating HNO signaling and its interaction with H2S.
Conclusions:
- The developed HNO generators are valuable tools for studying short-lived gaseous signaling molecules.
- These tools will advance the understanding of HNO's role in cellular processes and disease.
- Further research into the cross-talk of signaling molecules like HNO and H2S is warranted.

