A Reporter of UV Intensity Delivered to the Cytosol during Photolytic Uncaging

被引:6
作者
Brasen, Jens Christian [1 ,2 ]
Dewitt, Sharon [1 ]
Hallett, Maurice B. [1 ]
机构
[1] Cardiff Univ, Neutrophil Signalling Grp, Sch Med, Cardiff, S Glam, Wales
[2] Univ So Denmark, Inst Biochem & Mol Biol, Odense, Denmark
基金
英国惠康基金;
关键词
HYDROETHIDINE; SUPEROXIDE; FLUORESCENCE; NEUTROPHILS; PRODUCT; SIGNALS; CELLS;
D O I
10.1016/j.bpj.2009.12.4271
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
Photolytic uncaging of biologically-active molecules within cells is a powerful technique. However, the delivery of uncaging light into the cytosol can vary between cell types, individual cells of the same type, and different loci within an individual cell because of optical differences in absorbance and light-scattering properties of the cytoplasm. Here, we demonstrate a simple technique for monitoring the magnitude of cytosolic ultraviolet delivery during uncaging, which also leaves a quantitative and persistent record of this within the cells. The simple method shown here provides a much needed universal monitor of the delivery of ultraviolet light to molecules within the cytosol, providing a much needed parameter for the correct interpretation of uncaging experiments.
引用
收藏
页码:L25 / L27
页数:3
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