Literature DB >> 25431060

Real-time visualization of caspase-3 activation by fluorescence resonance energy transfer (FRET).

Silvia Alasia1, Carolina Cocito, Adalberto Merighi, Laura Lossi.   

Abstract

As apoptosis occurs via a complex signaling cascade that is tightly regulated at multiple cell points, different methods exist to evaluate the activity of the proteins involved in the intracellular apoptotic pathways and the phenotype of apoptotic neurons. Detention of the activity of the enzyme caspase-3, the key executioner caspase in programmed cell death, by laser scanning confocal fluorescence microscopy and the fluorescence resonance energy transfer technology is an alternative approach to classical standard techniques, such as Western blotting, activity assays, or histological techniques, and allows working with both fixed and living cells. This technique combined with the organotypic culture approach ex vivo represents a valid tool for the study of the mechanisms of neuronal survival /death and neuroprotection.

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Year:  2015        PMID: 25431060     DOI: 10.1007/978-1-4939-2152-2_8

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  Ex vivo imaging of active caspase 3 by a FRET-based molecular probe demonstrates the cellular dynamics and localization of the protease in cerebellar granule cells and its regulation by the apoptosis-inhibiting protein survivin.

Authors:  Laura Lossi; Carolina Cocito; Silvia Alasia; Adalberto Merighi
Journal:  Mol Neurodegener       Date:  2016-04-28       Impact factor: 14.195

  1 in total

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