Gold Fluorescent Annexin A5 as a Novel Apoptosis Detection Tool

被引:10
作者
Kurschus, Florian C. [1 ]
Pal, Prajna Paramita [2 ]
Baeumler, Petra [2 ]
Jenne, Dieter E.
Wiltschi, Birgit [2 ]
Budisa, Nediljko [2 ]
机构
[1] Max Planck Inst Neurobiol, Dept Neuroimmunol, D-82125 Martinsried, Germany
[2] Max Planck Inst Biochem, D-82125 Martinsried, Germany
关键词
apoptosis; annexin; gold fluorescent protein; flow cytometry; FLOW-CYTOMETRIC DETECTION; ANTICOAGULANT PROTEIN-I; PHOSPHOLIPID-BINDING; PHOSPHATIDYLSERINE EXPRESSION; GRANZYME-B; CELLS; TRYPTOPHAN; CALCIUM; ASSAY;
D O I
10.1002/cyto.a.20737
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe a golden fluorescent apoptosis detection tool, which we generated by a fusion of golden fluorescent protein (GdFP) with human annexin A5 (anxA5). GdFP was obtained by replacement of tryptophan at position 66 with 4-aminotryptophan in the chromophore of enhanced cyan fluorescent protein. The GdFP-anxA5 construct combines highly desirable features originating from both fusion partners. These include (i) strong binding to membrane phosphatidylserine patches of apoptotic cells in the presence of Ca2+ which is brought about by anxA5, (ii) the stable and homogeneous monomeric state, (iii) as well as the red-shifted fluorescence maximum at 574 nm originating from GdFP. We found that GdFP-anxA5 is equally well applicable for apoptosis studies as a routinely used fluorescein 5'-isothiocyanate-annexin A5 conjugate. Golden fluorescent annexin A5 represents a new, stable, and homogeneous red-shifted optical probe for the efficient detection of apoptosis by fluorescence microscopy or by flow cytometry. (C) 2009 International Society for Advancement of Cytometry
引用
收藏
页码:626 / 633
页数:8
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