Two postprocessing techniques for the elimination of background autofluorescence for fluorescence lifetime imaging microscopy
Year: 2008
Type: article
Abstract: The analysis of fluorescence lifetime imaging microscopy (FLIM) data under complex biological conditions can be challenging. Particularly, the presence of short-lived autofluorescent aggregates can confound lifetime measurements in fluorescence energy transfer (FRET) experiments, where it can become confused with the signal from exogenous fluorophores. Here we report two techniques that can be used to discriminate the contribution of autofluorescence from exogenous fluorphores in FLIM. We apply the techniques to transgenic mice that natively express yellow fluorescence protein (YFP) in a subset of cortical neurons and to histological slices of aged human brain tissue, where we study the misfolding of intracellular tau protein in the form of neurofibrillary tangles.
Source: Journal of Biomedical Optics
DOI: 10.1117/1.2837169
Language: English
Subfield: Biophysics
Domain: Life Sciences
Open Access status: bronze
Awards: G1412165948, Anatomical Changes in Tau Transgenic Models, G1915837458, G2132047791, G279242282, Multiphoton microscopy for in vivo neural imaging, G39712242, G4413556686, G6703509384, Non-invasive optical imaging of neuropathology in vivo, G7237067214, Molecular mechanism of Presenilin-1 (PS1) linked Alzheimer's Disease pathology, G9000140468, G9000220226, G9000313697, G942089662
OpenAlex ID: W2078437878
