| Literature DB >> 34748127 |
Yueling Zhang1, Juan Hu2, Meijuan Yu1, Zhirong Wang2, Hucheng Qing2, Huheng Fu3, Liudi Yuan2,1, Fei Li4, Sheng Zhao5,6.
Abstract
ANNEXIN V belongs to a family of phospholipid binding proteins which is able to bind to negatively charged phospholipids such as phosphatidylserine (PS) in the presence of a high affinity Ca2+ ion. When apoptosis occurs, even at early stage, PS will be exposed to the outside of the cell surface from the cytoplasm side of membrane leaflets., Therefore ANNEXIN V has been suggested as a bio-marker for imaging early apoptotic events of various cell death including those in disease conditions. However, most ANNEXIN V-based apoptotic detecting techniques were in vitro approaches. Here, we presented a new BRET (Bioluminescence Resonance Energy Transfer) based genetic coded biosensor by fusing ANNEXIN V and a BRET version of NanoLuc (teLuc) for both in vitro and in vivo apoptosis detection. The BRET feature of this new sensor makes it convenient to be applied to both conventional fluorescent-based in vitro apoptosis detection and bioluminescence-based animal live imaging for in vivo study. Because of its robust bioluminescence signal, it is possible to perform the evaluation of the disease-induced apoptotic damage and recovery process directly at deep tissue level in live animal.Entities:
Keywords: ANNEXIN V; Apoptosis; Bioluminescence; Biosensor; Fluorescence; Live imaging
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Year: 2021 PMID: 34748127 DOI: 10.1007/s10495-021-01693-x
Source DB: PubMed Journal: Apoptosis ISSN: 1360-8185 Impact factor: 4.677