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FRET-Based Ca 2+ Biosensor Single Cell Imaging Interrogated by High-Frequency Ultrasound
by
Shung, Kirk
, Wang, Yingxiao
, Pan, Yijia
, Yoon, Sangpil
in
Biosensing Techniques
/ Calcium - analysis
/ Cells, Cultured
/ Fluorescence Resonance Energy Transfer
/ Fluorescent Dyes
/ Humans
/ Ionomycin
/ Single-Cell Analysis
/ Ultrasonography
2020
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FRET-Based Ca 2+ Biosensor Single Cell Imaging Interrogated by High-Frequency Ultrasound
by
Shung, Kirk
, Wang, Yingxiao
, Pan, Yijia
, Yoon, Sangpil
in
Biosensing Techniques
/ Calcium - analysis
/ Cells, Cultured
/ Fluorescence Resonance Energy Transfer
/ Fluorescent Dyes
/ Humans
/ Ionomycin
/ Single-Cell Analysis
/ Ultrasonography
2020
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Do you wish to request the book?
FRET-Based Ca 2+ Biosensor Single Cell Imaging Interrogated by High-Frequency Ultrasound
by
Shung, Kirk
, Wang, Yingxiao
, Pan, Yijia
, Yoon, Sangpil
in
Biosensing Techniques
/ Calcium - analysis
/ Cells, Cultured
/ Fluorescence Resonance Energy Transfer
/ Fluorescent Dyes
/ Humans
/ Ionomycin
/ Single-Cell Analysis
/ Ultrasonography
2020
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FRET-Based Ca 2+ Biosensor Single Cell Imaging Interrogated by High-Frequency Ultrasound
Journal Article
FRET-Based Ca 2+ Biosensor Single Cell Imaging Interrogated by High-Frequency Ultrasound
2020
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Overview
Fluorescence resonance energy transfer (FRET)-based biosensors have advanced live cell imaging by dynamically visualizing molecular events with high temporal resolution. FRET-based biosensors with spectrally distinct fluorophore pairs provide clear contrast between cells during dual FRET live cell imaging. Here, we have developed a new FRET-based Ca
biosensor using EGFP and FusionRed fluorophores (FRET-GFPRed). Using different filter settings, the developed biosensor can be differentiated from a typical FRET-based Ca
biosensor with ECFP and YPet (YC3.6 FRET Ca
biosensor, FRET-CFPYPet). A high-frequency ultrasound (HFU) with a carrier frequency of 150 MHz can target a subcellular region due to its tight focus smaller than 10 µm. Therefore, HFU offers a new single cell stimulations approach for FRET live cell imaging with precise spatial resolution and repeated stimulation for longitudinal studies. Furthermore, the single cell level intracellular delivery of a desired FRET-based biosensor into target cells using HFU enables us to perform dual FRET imaging of a cell pair. We show that a cell pair is defined by sequential intracellular delivery of the developed FRET-GFPRed and FRET-CFPYPet into two target cells using HFU. We demonstrate that a FRET-GFPRed exhibits consistent 10-15% FRET response under typical ionomycin stimulation as well as under a new stimulation strategy with HFU.
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