Hyperspectral imaging for simultaneous measurements of two FRET biosensors in pancreatic β-cells.
Amicia D ElliottNoah BedardAlessandro UstioneMichelle A BairdMichael W DavidsonTomasz TkaczykDavid W PistonPublished in: PloS one (2017)
Fluorescent protein (FP) biosensors based on Förster resonance energy transfer (FRET) are commonly used to study molecular processes in living cells. There are FP-FRET biosensors for many cellular molecules, but it remains difficult to perform simultaneous measurements of multiple biosensors. The overlapping emission spectra of the commonly used FPs, including CFP/YFP and GFP/RFP make dual FRET measurements challenging. In addition, a snapshot imaging modality is required for simultaneous imaging. The Image Mapping Spectrometer (IMS) is a snapshot hyperspectral imaging system that collects high resolution spectral data and can be used to overcome these challenges. We have previously demonstrated the IMS's capabilities for simultaneously imaging GFP and CFP/YFP-based biosensors in pancreatic β-cells. Here, we demonstrate a further capability of the IMS to image simultaneously two FRET biosensors with a single excitation band, one for cAMP and the other for Caspase-3. We use these measurements to measure simultaneously cAMP signaling and Caspase-3 activation in pancreatic β-cells during oxidative stress and hyperglycemia, which are essential components in the pathology of diabetes.
Keyphrases
- energy transfer
- high resolution
- living cells
- induced apoptosis
- single molecule
- quantum dots
- fluorescent probe
- oxidative stress
- endoplasmic reticulum stress
- cell cycle arrest
- type diabetes
- cell death
- signaling pathway
- cardiovascular disease
- mass spectrometry
- machine learning
- magnetic resonance imaging
- metabolic syndrome
- insulin resistance
- photodynamic therapy
- electronic health record
- glycemic control
- heat shock protein
- molecular dynamics
- cell proliferation
- artificial intelligence
- dual energy
- amino acid