| Literature DB >> 34689421 |
Rozhin Penjweini1, Branden Roarke1, Greg Alspaugh1, Katie A Link1, Alessio Andreoni1,2, Mateus P Mori3, Paul M Hwang3, Dan L Sackett4, Jay R Knutson1.
Abstract
The biological relevance of nitric oxide (NO) and reactive oxygen species (ROS) in signaling, metabolic regulation, and disease treatment has become abundantly clear. The dramatic change in NO/ROS processing that accompanies a changing oxygen landscape calls for new imaging tools that can provide cellular details about both [O2 ] and the production of reactive species. Myoglobin oxidation to the met state by NO/ROS is a known sensor with absorbance changes in the visible range. We previously employed Förster resonance energy transfer to read out the deoxygenation/oxygenation of myoglobin, creating the subcellular [O2 ] sensor Myoglobin-mCherry. We now add the fluorescent protein EYFP to this sensor to create a novel probe that senses both met formation, a proxy for ROS/NO exposure, and [O2 ]. Since both proteins are present in the construct, it can also relieve users from the need to measure fluorescence lifetime, making [O2 ] sensing available to a wider group of laboratories.Entities:
Keywords: EYFP-Myoglobin-mCherry; FLIM; NO; ROS; metMb
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Year: 2021 PMID: 34689421 PMCID: PMC8901566 DOI: 10.1002/jbio.202100166
Source DB: PubMed Journal: J Biophotonics ISSN: 1864-063X Impact factor: 3.390