Premium
Theoretical background of light‐emitting diode total internal reflection fluorescence microscopy and photobleaching lifetime analysis of membrane‐associated proteins—Part II
Author(s) -
Schaefer Michael,
Kalwa Hermann
Publication year - 2020
Publication title -
journal of biophotonics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.877
H-Index - 66
eISSN - 1864-0648
pISSN - 1864-063X
DOI - 10.1002/jbio.201960181
Subject(s) - total internal reflection fluorescence microscope , photobleaching , microscopy , fluorescence recovery after photobleaching , optics , laser , materials science , microscope , laser diode , optoelectronics , fluorescence , diode , physics
The selective microscopic imaging of the plasma membrane and adjacent structures by total internal reflection fluorescence (TIRF) microscopy is a versatile and frequently used technique in cell biology. A reduction of imaging artifacts in objective‐type TIRF microscopy can be achieved by circular or multi‐spot laser illumination or by using noncoherent light sources that are projected into the back focal plane as a light annulus. Light‐emitting diode (LED)‐based TIRF excitation is a recent advancement of the latter strategy. While some basic principles of LED‐TIRF remain the same as in laser‐based methods, the calculation of penetration depth, the flatness of illumination and the amount of available illumination power differ. This study provides the theoretical framework for the construction and adjustment of LED‐TIRF. Using state‐of‐the art high power LED emitters, LED‐TIRF achieves excitation efficiencies that are comparable to laser‐based systems and homogenously illuminate the entire field of view, thus, allowing variation of the penetration depth or quantitative photobleaching‐assisted imaging protocols. Using autofluorescent transmembrane, soluble and membrane‐attached fusion proteins, we provide examples for a photobleaching‐based assessment of the exchange kinetics of proteins within living human endothelial cells.