scholarly journals Synthesis, Characterizations, and Intramolecular Quenching Behavior of an Axially-Linked Trinuclear Molecular Wire Containing Ruthenium(II) Porphycenes

2015 ◽  
Vol 4 (1) ◽  
pp. 22-24
Author(s):  
Masaaki Abe ◽  
Shiho Ashigara ◽  
Toru Okawara ◽  
Yoshio Hisaeda
2018 ◽  
Author(s):  
Steven Boggess ◽  
Shivaani Gandhi ◽  
Brian Siemons ◽  
Nathaniel Huebsch ◽  
Kevin Healy ◽  
...  

<div> <p>The ability to non-invasively monitor membrane potential dynamics in excitable cells like neurons and cardiomyocytes promises to revolutionize our understanding of the physiology and pathology of the brain and heart. Here, we report the design, synthesis, and application of a new class of fluorescent voltage indicator that makes use of a fluorene-based molecular wire as a voltage sensing domain to provide fast and sensitive measurements of membrane potential in both mammalian neurons and human-derived cardiomyocytes. We show that the best of the new probes, fluorene VoltageFluor 2 (fVF 2) readily reports on action potentials in mammalian neurons, detects perturbations to cardiac action potential waveform in human induced pluripotent stem cell (hiPSC)-derived cardiomyocytes, shows a substantial decrease in phototoxicity compared to existing molecular wire-based indicators, and can monitor cardiac action potentials for extended periods of time. Together, our results demonstrate the generalizability of a molecular wire approach to voltage sensing and highlights the utility of fVF 2 for interrogating membrane potential dynamics.</p> </div>


Author(s):  
Marcus Edwards ◽  
Gaye White ◽  
Julea Butt ◽  
David J. Richardson ◽  
Thomas A. Clarke
Keyword(s):  

2019 ◽  
Vol 523 ◽  
pp. 1-6
Author(s):  
Yuxiu Wang ◽  
Cuicui Sun ◽  
Zhao-Di Yang ◽  
Hong Yu ◽  
Ping Pan ◽  
...  

2010 ◽  
Vol 21 (12) ◽  
pp. 125706 ◽  
Author(s):  
J Andzane ◽  
J Prikulis ◽  
D Dvorsek ◽  
D Mihailovic ◽  
D Erts
Keyword(s):  

1992 ◽  
Vol 57 (1) ◽  
pp. 26-32 ◽  
Author(s):  
N. M. Guindy ◽  
F. M. Elzawawy ◽  
D. Y. Sabry

The photochemistry of free-base meso-tetraphenylporphyrin linked to methyl viologen via an alkoxy chain (n = 3) at the ortho, meta or para-position of one meso-phenyl group, in Triton X-100 micellar aqueous solutions is reported. The appended viologen does not quench the porphyrin fluorescence nor its triplet excited state due to the different solubilization of both parts of the molecule in the medium where the porphyrin ring resides in the hydrophobic phase and the alkoxy linker protrudes into the rather diffuse outer phase of detergent oxyethylene units, while the viologen moiety penetrates into the aqueous layer. However, laser flash photolysis measurements show that in the presence of nicotinamide dinucleotide, NADH, the porphyrin ring is reduced to phlorin due to the penetration of NADH into the organic phase. For porphyrin-tetraviologen in which a viologen molecule is linked to each of the porphyrin meso-position via alkoxy chain, fluorescence quenching could be achieved. The values of the quenching efficiency are high (94% in acetonitrile) compared to intramolecular quenching and are dependent upon the solvent viscosity.


2001 ◽  
Vol 79 (22) ◽  
pp. 3708-3710 ◽  
Author(s):  
Hiroshi Sakaguchi ◽  
Atsushi Hirai ◽  
Futoshi Iwata ◽  
Akira Sasaki ◽  
Toshihiko Nagamura ◽  
...  

2003 ◽  
Vol 19 (1) ◽  
pp. 23-26 ◽  
Author(s):  
Shawn D. WETTIG ◽  
Chen-Zhong LI ◽  
Yi-Tao LONG ◽  
Heinz-Bernhard KRAATZ ◽  
Jeremy S. LEE

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