scholarly journals Fluorescence Cross-Correlation Spectroscopy for Real-Time Monitoring of Exogenous DNA Behavior in Living Cells

10.5772/18970 ◽  
2011 ◽  
Author(s):  
Akira Sasaki ◽  
Masataka Kinjo
Keyword(s):  
Real Time ◽  
Cross Correlation ◽  
Living Cells ◽  
Correlation Spectroscopy ◽  
Real Time Monitoring ◽  
Exogenous Dna

A multicolor DNA tetrahedron nanoprobe for analyzing human telomerase in living cells

2021 ◽  
Author(s):  
Ruiyuan Zhang ◽  
Ruixue Zhang ◽  
Wei Jiang ◽  
Xiaowen Xu
Keyword(s):  
Real Time ◽  
Length Distribution ◽  
Telomerase Activity ◽  
Living Cells ◽  
Real Time Monitoring ◽  
Dna Tetrahedron ◽  
Human Telomerase

A sequentially lighting-up multicolor DNA tetrahedron nanoprobe is constructed for imaging telomerase activity, real-time monitoring telomerase action and determining product length distribution in living cells.

A novel microfluidic microelectrode chip for a significantly enhanced monitoring of NPY-receptor activation in live mode

Lab on a Chip ◽  
2017 ◽  
Vol 17 (24) ◽  
pp. 4294-4302 ◽  
Author(s):  
Franziska D. Zitzmann ◽  
Heinz-Georg Jahnke ◽  
Felix Nitschke ◽  
Annette G. Beck-Sickinger ◽  
Bernd Abel ◽  
...  
Keyword(s):  
Real Time ◽  
Microfluidic Chip ◽  
Microelectrode Array ◽  
Fem Simulation ◽  
Receptor Activation ◽  
Living Cells ◽  
Real Time Monitoring ◽  
Non Invasive ◽  
Npy Receptor ◽  
Simulation Based

We present a FEM simulation based step-by-step development of a microelectrode array integrated into a microfluidic chip for the non-invasive real-time monitoring of living cells.

scholarly journals Designing, construction and characterization of genetically encoded FRET-based nanosensor for real time monitoring of lysine flux in living cells

2016 ◽  
Vol 14 (1) ◽  
Author(s):  
Seema Ameen ◽  
Mohammad Ahmad ◽  
Mohd. Mohsin ◽  
M. Irfan Qureshi ◽  
Mohamed M. Ibrahim ◽  
...  
Keyword(s):  
Real Time ◽  
Living Cells ◽  
Real Time Monitoring

scholarly journals Multi-color fluorescence fluctuation spectroscopy in living cells via spectral detection

2020 ◽  
Author(s):  
Valentin Dunsing ◽  
Annett Petrich ◽  
Salvatore Chiantia
Keyword(s):  
Correlation Analysis ◽  
Influenza A ◽  
Cross Correlation ◽  
Matrix Protein ◽  
Living Cells ◽  
Correlation Spectroscopy ◽  
Image Correlation ◽  
Fluorescence Fluctuation Spectroscopy ◽  
Diffusion Dynamics ◽  
Cross Correlation Analysis

AbstractFluorescence fluctuation spectroscopy provides a powerful toolbox to quantify transport dynamics and interactions between biomolecules in living cells. For example, cross-correlation analysis of spectrally separated fluctuations allows the investigation of inter-molecular interactions. This analysis is conventionally limited to two fluorophore species that are excited with a single or two different laser lines and detected in two non-overlapping spectral channels. However, signaling pathways in biological systems often involve interactions between multiple biomolecules, e.g. formation of ternary or quaternary protein complexes. Here, we present a methodology to investigate such interactions at the plasma membrane (PM) of cells, as encountered for example in viral assembly or receptor-ligand interactions. To this aim, we introduce scanning fluorescence spectral correlation spectroscopy (SFSCS), a combination of scanning fluorescence correlation spectroscopy with spectrally resolved detection and decomposition. We first demonstrate that SFSCS allows cross-talk-free cross-correlation analysis of PM-associated proteins labeled with strongly overlapping fluorescent proteins (FPs), such as mEGFP and mEYFP, excited with a single excitation line. We then verify the applicability of SFSCS for quantifying diffusion dynamics and protein oligomerization (based on molecular brightness analysis) of two protein species tagged with spectrally overlapping FPs. Adding a second laser line, we demonstrate the possibility of three- and four-species (cross-) correlation analysis using mApple and mCherry2, as examples of strongly overlapping FP tags in the red spectral region. Next, we apply this scheme to investigate the interactions of influenza A virus (IAV) matrix protein 2 (M2) with two cellular host factors simultaneously. Using the same set of fluorophores, we furthermore extend the recently presented raster spectral image correlation spectroscopy (RSICS) approach to four species analysis, successfully demonstrating multiplexed RSICS measurements of protein interactions in the cell cytoplasm. Finally, we apply RSICS to investigate the assembly of the ternary IAV polymerase complex and report a 2:2:2 stoichiometry of these protein assemblies in the nucleus of living cells.

Real-time monitoring of endogenous cysteine levels in living cells using a CD-based ratiometric fluorescent nanoprobe

2018 ◽  
Vol 410 (18) ◽  
pp. 4379-4386 ◽  
Author(s):  
Hong Wang ◽  
Peisheng Zhang ◽  
Yong Tian ◽  
Yuan Zhang ◽  
Heping Yang ◽  
...  
Keyword(s):  
Real Time ◽  
Living Cells ◽  
Real Time Monitoring ◽  
Fluorescent Nanoprobe
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