scholarly journals Over the rainbow: A practical guide for fluorescent protein selection in plant FRET experiments

Plant Direct ◽  
2019 ◽  
Vol 3 (12) ◽  
Author(s):  
Grégoire Denay ◽  
Patrick Schultz ◽  
Sebastian Hänsch ◽  
Stefanie Weidtkamp‐Peters ◽  
Rüdiger Simon

Author(s):  
Andreas Margraf ◽  
Markus Sperandio

In vivo observations of blood cells and organ compartments within the fetal mammalian organism are difficult to obtain. This practical guide describes a mouse model for in vivo observation of the fetal yolk-sac and corporal microvasculature throughout murine gestation, including imaging of various organ compartments, microvascular injection procedures, different methods for staining of blood plasma, vessel wall and circulating cell subsets. Following anesthesia of pregnant mice, the maternal abdominal cavity is opened, the uterus horn exteriorized, and the fetus prepared for imaging while still connected to the placenta. Microinjection methods allow delivery of substances directly into the fetal circulation, while substances crossing the placenta can be easily administered via the maternal circulation. Small volume blood sample collection allows for further in vitro workup of obtained results. The model permits observation of leukocyte-endothelial interactions, hematopoietic niche localization, platelet function, endothelial permeability studies, and hemodynamic changes in the mouse fetus, using appropriate strains of fluorescent protein expressing reporter mice and various sophisticated intravital microscopy techniques. Our practical guide is of interest to basic physiologists, developmental biologists, cardiologists, and translational neonatologists and reaches out to scientists focusing on the origin and regulation of hematopoietic niches, thrombopoiesis and macrophage heterogeneity.



PLoS ONE ◽  
2019 ◽  
Vol 14 (3) ◽  
pp. e0212956 ◽  
Author(s):  
Colin Q. Lischik ◽  
Leonie Adelmann ◽  
Joachim Wittbrodt


2009 ◽  
Vol 28 (3) ◽  
pp. 103-108 ◽  
Author(s):  
Sergei Popov ◽  
Saied Mirshahidi ◽  
Sosthène Essono ◽  
Ruijiang Song ◽  
Xiaowei Wang ◽  
...  


2020 ◽  
Vol 48 (6) ◽  
pp. 2657-2667
Author(s):  
Felipe Montecinos-Franjola ◽  
John Y. Lin ◽  
Erik A. Rodriguez

Noninvasive fluorescent imaging requires far-red and near-infrared fluorescent proteins for deeper imaging. Near-infrared light penetrates biological tissue with blood vessels due to low absorbance, scattering, and reflection of light and has a greater signal-to-noise due to less autofluorescence. Far-red and near-infrared fluorescent proteins absorb light >600 nm to expand the color palette for imaging multiple biosensors and noninvasive in vivo imaging. The ideal fluorescent proteins are bright, photobleach minimally, express well in the desired cells, do not oligomerize, and generate or incorporate exogenous fluorophores efficiently. Coral-derived red fluorescent proteins require oxygen for fluorophore formation and release two hydrogen peroxide molecules. New fluorescent proteins based on phytochrome and phycobiliproteins use biliverdin IXα as fluorophores, do not require oxygen for maturation to image anaerobic organisms and tumor core, and do not generate hydrogen peroxide. The small Ultra-Red Fluorescent Protein (smURFP) was evolved from a cyanobacterial phycobiliprotein to covalently attach biliverdin as an exogenous fluorophore. The small Ultra-Red Fluorescent Protein is biophysically as bright as the enhanced green fluorescent protein, is exceptionally photostable, used for biosensor development, and visible in living mice. Novel applications of smURFP include in vitro protein diagnostics with attomolar (10−18 M) sensitivity, encapsulation in viral particles, and fluorescent protein nanoparticles. However, the availability of biliverdin limits the fluorescence of biliverdin-attaching fluorescent proteins; hence, extra biliverdin is needed to enhance brightness. New methods for improved biliverdin bioavailability are necessary to develop improved bright far-red and near-infrared fluorescent proteins for noninvasive imaging in vivo.





Author(s):  
Elizabeth Louise Mansfield
Keyword(s):  


1973 ◽  
Vol 18 (11) ◽  
pp. 566-566
Author(s):  
N. L. GAGE






1978 ◽  
Vol 23 (9) ◽  
pp. 687-688
Author(s):  
SHIRLEY SANDERS
Keyword(s):  


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