Live cell imaging with Surface Plasmon-Mediated Fluorescence Microscopy

Author(s):  
Karla Balaa ◽  
Viviane Devauges ◽  
Yannick Goulam ◽  
Vincent Studer ◽  
Sandrine Lévêque-Fort ◽  
...  
2009 ◽  
Author(s):  
Karla Balaa ◽  
Viviane Devauges ◽  
Yannick Goulam ◽  
Vincent Studer ◽  
Sandrine Lévêque-Fort ◽  
...  

2011 ◽  
Vol 36 (16) ◽  
pp. 3051 ◽  
Author(s):  
Thomas Barroca ◽  
Karla Balaa ◽  
Julie Delahaye ◽  
Sandrine Lévêque-Fort ◽  
Emmanuel Fort

2019 ◽  
Vol 12 (1) ◽  
Author(s):  
Dulanthi Weerasekera ◽  
Jonas Hahn ◽  
Martin Herrmann ◽  
Andreas Burkovski

Abstract Objectives In frame of a study to characterize the interaction of human macrophage-like cells with pathogenic corynebacteria, Corynebacterium diphtheriae and Corynebacterium ulcerans, live cell imaging experiments were carried out and time lapse fluorescence microscopy videos were generated, which are presented here. Data description The time lapse fluorescence microscopy data revealed new insights in the interaction of corynebacteria with human macrophage-like THP-1 cells. In contrast to uninfected cells and infections with non-pathogenic C. glutamicum used as a control, pathogenic C. diphtheriae and C. ulcerans showed highly detrimental effects towards human cells and induction of cell death of macrophages.


2021 ◽  
Author(s):  
Michelle S. Frei ◽  
Miroslaw Tarnawski ◽  
M. Julia Roberti ◽  
Birgit Koch ◽  
Julien Hiblot ◽  
...  

AbstractSelf-labeling protein tags such as HaloTag are powerful tools that can label fusion proteins with synthetic fluorophores for use in fluorescence microscopy. Here we introduce HaloTag variants with either increased or decreased brightness and fluorescence lifetime compared with HaloTag7 when labeled with rhodamines. Combining these HaloTag variants enabled live-cell fluorescence lifetime multiplexing of three cellular targets in one spectral channel using a single fluorophore and the generation of a fluorescence lifetime-based biosensor. Additionally, the brightest HaloTag variant showed up to 40% higher brightness in live-cell imaging applications.


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