Abstract
Molecular rotors are fluorophores that have a fluorescence quantum yield that depends upon intermolecular rotation. The fluorescence quantum yield, intensity and lifetime of molecular rotors all vary as functions of viscosity, as high viscosities inhibit intermolecular rotation and cause an increase in the non-radiative decay rate. As such, molecular rotors can be used to probe viscosity on microscopic scales. Here, we apply fluorescence lifetime imaging microscopy (FLIM) to measure the fluorescence lifetimes of three different molecular rotors, in order to determine the microscopic viscosity in two model systems with significant biological interest. First, the constituents of a novel protocell - a model of a prebiotic cell - were studied using the molecular rotors BODIPY C10 and kiton red. Second, amyloid formation was investigated using the molecular rotor Cy3.
Original language | English |
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Title of host publication | Progress in Biomedical Optics and Imaging - Proceedings of SPIE |
Publisher | Society of Photo-Optical Instrumentation Engineers (SPIE) |
Volume | 8947 |
ISBN (Print) | 9780819498601 |
DOIs | |
Publication status | Published - 1 Jan 2014 |
Event | Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues XII - San Francisco, CA, United Kingdom Duration: 3 Feb 2014 → 6 Feb 2014 |
Conference
Conference | Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues XII |
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Country/Territory | United Kingdom |
City | San Francisco, CA |
Period | 3/02/14 → 6/02/14 |
Keywords
- Amyloid
- Confocal microscopy
- Flim
- Fluorescence
- Fluorescence lifetime
- Lysozyme
- Molecular rotor
- Neurodegeneration
- Protein aggregation
- Protocells
- Viscosity