Spectral Unmixing of Flavin Autofluorescence Components in Cardiac Myocytes

Abstract

AbstractWe applied linear unmixing approach to reveal individual components of intrinsic flavin fluorescence signal recorded in living cardiac cells by spectrally resolved confocal microscopy. Responses of whole-cell autofluorescence to modulators of cell metabolism and respiration were used as a tool of separation of its components; their spectral profiles, estimated by principal component analysis, correspond to free FAD and FAD bound to different enzymes of electron transport chain

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This paper was published in Elsevier - Publisher Connector .

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