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1 May 2007 Sub-cell FRET imaging for determination of signaling pathway of cell apoptosis during tumor therapy
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Proceedings Volume 6534, Fifth International Conference on Photonics and Imaging in Biology and Medicine; 653402 (2007) https://doi.org/10.1117/12.741092
Event: Fifth International Conference on Photonics and Imaging in Biology and Medicine, 2006, Wuhan, China
Abstract
The current advances in fluorescence microscopy, coupled with the development of new fluorescent probes, make fluorescence resonance energy transfer (FRET) a powerful technique for studying molecular interactions inside living cells with improved spatial and temporal resolution, distance range, and sensitivity and a broader range of biological applications. In recent years, a large number of studies have been conducted aiming to understand the process of apoptosis during tumor therapy on a molecular basis. Here, we utilized a recombinant FRET Bid probe to determine the kinetics of Bid cleavage during Cisplatin-induced apoptosis in ASTC-a-1 cells. Cells treated with Cisplatin (20 μM) showed a cleavage of the Bid-FRET probe, occurring at about 4-5 h after onset of the Cisplatin exposure, and lasted about 1.5 h. Our data clearly showed the kinetics of Bid cleavage during Cisplatin-induced apoptosis. We also used FRET technique to measure the dynamics of caspase-3 activation during apoptosis induced by high fluence low-power laser irradiation (LPLI). The data showed that we can detect caspase-3 activation sensitively and effectively, by using the FRET probe SCAT3.
© (2007) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Lei Liu D.D.S., Da Xing, and Wei R. Chen "Sub-cell FRET imaging for determination of signaling pathway of cell apoptosis during tumor therapy", Proc. SPIE 6534, Fifth International Conference on Photonics and Imaging in Biology and Medicine, 653402 (1 May 2007); https://doi.org/10.1117/12.741092
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KEYWORDS
Fluorescence resonance energy transfer

Cell death

Luminescence

Tumors

Fluorescent proteins

Laser therapeutics

Molecules

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