scholarly journals An alternative in vitro drug screening test using Leishmania amazonensis transfected with red fluorescent protein

2013 ◽  
Vol 75 (3) ◽  
pp. 282-291 ◽  
Author(s):  
Marcele N. Rocha ◽  
Célia M. Corrêa ◽  
Maria N. Melo ◽  
Stephen M. Beverley ◽  
Olindo Assis Martins-Filho ◽  
...  
2017 ◽  
Vol 2017 ◽  
pp. 1-11 ◽  
Author(s):  
Andrés Vacas ◽  
Conor Sugden ◽  
Óscar Velasco-Rodriguez ◽  
Miriam Algarabel-Olona ◽  
José Peña-Guerrero ◽  
...  

Leishmania is the causative agent of leishmaniasis, a neglected tropical disease that affects more than 12 million people around the world. Current treatments are toxic and poorly effective due to the acquisition of resistance within Leishmania populations. Thus, the pursuit for new antileishmanial drugs is a priority. The available methods for drug screening based on colorimetric assays using vital dyes are time-consuming. Currently, the use of fluorescent reporter proteins is replacing the use of viability indicator dyes. We have constructed two plasmids expressing the red fluorescent protein mCherry with multiple cloning sites (MCS), adequate for N- and C-terminal fusion protein constructs. Our results also show that the improved pXG-mCherry plasmid can be employed for drug screening in vitro. The use of the red fluorescent protein, mCherry, is an easier tool for numerous assays, not only to test pharmacological compounds, but also to determine the subcellular localization of proteins.


2018 ◽  
Vol 44 ◽  
pp. S110
Author(s):  
T. Agarwal ◽  
T. Maiti ◽  
S. Ghosh

2020 ◽  
Vol 9 (7) ◽  
pp. 1901773 ◽  
Author(s):  
Jing Nie ◽  
Qing Gao ◽  
Jianzhong Fu ◽  
Yong He

1984 ◽  
Vol 6 (5) ◽  
pp. 709-716 ◽  
Author(s):  
M. V. Mankar ◽  
R. Jagannathan ◽  
P. R. Mahadevan

2013 ◽  
Vol 65 (11-12) ◽  
pp. 1575-1588 ◽  
Author(s):  
Jonathan H. Tsui ◽  
Woohyuk Lee ◽  
Suzie H. Pun ◽  
Jungkyu Kim ◽  
Deok-Ho Kim

2007 ◽  
Vol 15 (3) ◽  
pp. 3-5
Author(s):  
Stephen W. Carmichael

How do lumens form? Two mechanisms that come readily to mind are a wrapping model, similar to the wrapping of the myelin sheath around a neuronal process, and a solid core of cells followed by apoptosis of the central cells. Another obvious mechanism that was suggested over 100 years ago is the fusion of intracellular vacuoles. Whereas several recent studies have supported this latter mechanism, it has not yet been proven. Now, the appropriate animal model (zebrafish), the modern techniques (transgenic chimeras), dyes (green fluorescent protein and monomeric red fluorescent protein) that can be linked to proteins to label vacuoles, and two-photon imaging in real time finally have provided the strongest support yet. In an article by Makoto Kamei, Brian Saunders, Kayla Bayless, Louis Dye, George Davis, and Brant Weinstein the assembly of endothelial tubes from intracellular vacuoles was observed in vitro and in vivo.


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