| Literature DB >> 25361143 |
Simon P Poland, Nikola Krstajić, Simao Coelho, David Tyndall, Richard J Walker, Viviane Devauges, Penny E Morton, Nicole S Nicholas, Justin Richardson, David Day-Uei Li, Klaus Suhling, Claire M Wells, Maddy Parsons, Robert K Henderson, Simon M Ameer-Beg.
Abstract
Imaging the spatiotemporal interaction of proteins in vivo is essential to understanding the complexities of biological systems. The highest accuracy monitoring of protein-protein interactions is achieved using Förster resonance energy transfer (FRET) measured by fluorescence lifetime imaging, with measurements taking minutes to acquire a single frame, limiting their use in dynamic live cell systems. We present a diffraction limited, massively parallel, time-resolved multifocal multiphoton microscope capable of producing fluorescence lifetime images with 55 ps time-resolution, giving improvements in acquisition speed of a factor of 64. We present demonstrations with FRET imaging in a model cell system and demonstrate in vivo FLIM using a GTPase biosensor in the zebrafish embryo.Entities:
Mesh:
Year: 2014 PMID: 25361143 DOI: 10.1364/OL.39.006013
Source DB: PubMed Journal: Opt Lett ISSN: 0146-9592 Impact factor: 3.776