Simultaneous time and frequency resolved fluorescence microscopy of single molecules.

Hayden, Carl C. ; Gradinaru, Claudiu C. ; Chandler, David W. ; Luong, A. Khai

Sandia National Laboratories

关键词: Decay;    Photons;    Fluorescence;    Wavelengths Molecular Dynamics.;    Pmma;   

DOI  :  10.2172/921607
RP-ID  :  SAND2005-0036
RP-ID  :  AC04-94AL85000
RP-ID  :  921607

美国|英语

来源: UNT Digital Library

【 摘 要 】

Single molecule fluorophores were studied for the first time with a new confocal fluorescence microscope that allows the wavelength and emission time to be simultaneously measured with single molecule sensitivity. In this apparatus, the photons collected from the sample are imaged through a dispersive optical system onto a time and position sensitive detector. This detector records the wavelength and emission time of each detected photon relative to an excitation laser pulse. A histogram of many events for any selected spatial region or time interval can generate a full fluorescence spectrum and correlated decay plot for the given selection. At the single molecule level, this approach makes entirely new types of temporal and spectral correlation spectroscopy of possible. This report presents the results of simultaneous time- and frequency-resolved fluorescence measurements of single rhodamine 6G (R6G), tetramethylrhodamine (TMR), and Cy3 embedded in thin films of polymethylmethacrylate (PMMA).