scholarly journals A switchable peptide sensor for real-time lysosomal tracking

2014 ◽  
Vol 50 (49) ◽  
pp. 6443-6446 ◽  
Author(s):  
Lei Chen ◽  
Junchen Wu ◽  
Carsten Schmuck ◽  
He Tian

A bis-spiropyran functionalized peptide1, which exhibits good cell-permeability, biocompatibility and low cytotoxicity, has been developed for lysosomal tracking.

2019 ◽  
Vol 43 (8) ◽  
pp. 3303-3308 ◽  
Author(s):  
Sima Paul ◽  
Rajesh Nandi ◽  
Kakali Ghoshal ◽  
Maitree Bhattacharyya ◽  
Dilip K. Maiti

A newly designed and synthesized probe showed good cell permeability, low cytotoxicity, fast fluorogenic recognition, and “naked-eye” detection of a lethal health hazard, hydrazine, even at concentrations significantly below the TLV levels present in living cells, drinking water and industrial effluent.


2018 ◽  
Vol 16 (47) ◽  
pp. 9197-9203 ◽  
Author(s):  
Chunchao Tang ◽  
Lei Jin ◽  
Yuxing Lin ◽  
Jing Su ◽  
Yingai Sun ◽  
...  

We report a new BL probe,TyrBP-3, which not only exhibits high sensitivity and selectivity for imaging tyrosinase in vitro, and good cell-permeability for detecting tyrosinase in living cells, but can also visualize the level of tyrosinase activity in tumors of living animals.


2013 ◽  
Vol 133 (5) ◽  
pp. 3496-3496
Author(s):  
Pavlos Anastasiadis ◽  
Michelle L. Matter ◽  
John S. Allen

2021 ◽  
Vol 22 (22) ◽  
pp. 12542
Author(s):  
Oxana Kazakova ◽  
Roxana Racoviceanu ◽  
Anastasiya Petrova ◽  
Marius Mioc ◽  
Adrian Militaru ◽  
...  

Twenty lupane type A-ring azepano-triterpenoids were synthesized from betulin and its related derivatives and their antitubercular activity against Mycobacterium tuberculosis, mono-resistant MTB strains, and nontuberculous strains Mycobacterium abscessus and Mycobacterium avium were investigated in the framework of AToMIc (Anti-mycobacterial Target or Mechanism Identification Contract) realized by the Division of Microbiology and Infectious Diseases, NIAID, National Institute of Health. Of all the tested triterpenoids, 17 compounds showed antitubercular activity and 6 compounds were highly active on the H37Rv wild strain (with MIC 0.5 µM for compound 7), out of which 4 derivatives also emerged as highly active compounds on the three mono-resistant MTB strains. Molecular docking corroborated with a machine learning drug-drug similarity algorithm revealed that azepano-triterpenoids have a rifampicin-like antitubercular activity, with compound 7 scoring the highest as a potential M. tuberculosis RNAP potential inhibitor. FIC testing demonstrated an additive effect of compound 7 when combined with rifampin, isoniazid and ethambutol. Most compounds were highly active against M. avium with compound 14 recording the same MIC value as the control rifampicin (0.0625 µM). The antitubercular ex vivo effectiveness of the tested compounds on THP-1 infected macrophages is correlated with their increased cell permeability. The tested triterpenoids also exhibit low cytotoxicity and do not induce antibacterial resistance in MTB strains.


2018 ◽  
Vol 4 (11) ◽  
pp. eaau6972 ◽  
Author(s):  
Hyungjun Kim ◽  
Hanmin Jang ◽  
Bongjoong Kim ◽  
Min Ku Kim ◽  
Dae Seung Wie ◽  
...  

Vertically ordered arrays of silicon nanoneedles (Si NNs), due to their nanoscale dimension and low cytotoxicity, could enable minimally invasive nanoinjection of biomolecules into living biological systems such as cells and tissues. Although production of these Si NNs on a bulk Si wafer has been achieved through standard nanofabrication technology, there exists a large mismatch at the interface between the rigid, flat, and opaque Si wafer and soft, curvilinear, and optically transparent biological systems. Here, we report a unique methodology that is capable of constructing vertically ordered Si NNs on a thin layer of elastomer patch to flexibly and transparently interface with biological systems. The resulting outcome provides important capabilities to form a mechanically elastic interface between Si NNs and biological systems, and simultaneously enables direct imaging of their real-time interactions under the transparent condition. We demonstrate its utility in intracellular, intradermal, and intramuscular nanoinjection of biomolecules into various kinds of biological cells and tissues at their length scales.


Viruses ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1193
Author(s):  
Jorge L. Arias-Arias ◽  
Eugenia Corrales-Aguilar ◽  
Rodrigo A. Mora-Rodríguez

Conventional plaque assays rely on the use of overlays to restrict viral infection allowing the formation of distinct foci that grow in time as the replication cycle continues leading to countable plaques that are visualized with standard techniques such as crystal violet, neutral red, or immunolabeling. This classical approach takes several days until large enough plaques can be visualized and counted with some variation due to subjectivity in plaque recognition. Since plaques are clonal lesions produced by virus-induced cytopathic effect, we applied DNA fluorescent dyes with differential cell permeability to visualize them by live-cell imaging. We could observe different stages of that cytopathic effect corresponding to an early wave of cells with chromatin-condensation followed by a wave of dead cells with membrane permeabilization within plaques generated by different animal viruses. This approach enables an automated plaque identification using image analysis to increase single plaque resolution compared to crystal violet counterstaining and allows its application to plaque tracking and plaque reduction assays to test compounds for both antiviral and cytotoxic activities. This fluorescent real-time plaque assay sums to those next-generation technologies by combining this robust classical method with modern fluorescence microscopy and image analysis approaches for future applications in virology.


2017 ◽  
Vol 41 (20) ◽  
pp. 11507-11511 ◽  
Author(s):  
Kai Zhou ◽  
Mingguang Ren ◽  
Beibei Deng ◽  
Weiying Lin

Through rational design, two new mitochondria-targeted fluorescent viscosity probes were developed, which exhibited favorable properties such as large turn on fluorescence signal, good selectivity, low cytotoxicity, and high colocation coefficient (>0.90).


Author(s):  
Jorge L. Arias-Arias ◽  
Eugenia Corrales-Aguilar ◽  
Rodrigo Mora-Rodríguez

Conventional plaque assays rely on the use of overlays to restrict viral infection allowing the formation of distinct foci that grow in time as the replication cycle continues leading to counta-ble plaques that are visualized with standard techniques such as crystal violet, neutral red or immunolabeling. This classical approach takes several days until large enough plaques can be visualized and counted with some variation due to subjectivity in plaque recognition. Since plaques are clonal lesions produced by virus-induced cytopathic effect, we applied DNA fluores-cent dyes with differential cell permeability to visualize them by live cell imaging. We could observe different stages of that cytopathic effect corresponding to an early wave of cells with chromatin-condensation followed by a wave of dead cells with membrane permeabilization within plaques generated by different animal viruses. This approach enables an automated plaque identification using image analysis to increase single plaque resolution compared to crystal violet counterstaining and allows its application to plaque tracking and plaque reduction assays to test compounds for both antiviral and cytotoxic activities. This fluorescent real-time plaque assay sums to those next-generation technologies by combining this robust classical method with modern fluorescence microscopy and image analysis approaches for future applica-tions in virology.


2019 ◽  
Vol 43 (23) ◽  
pp. 9021-9031 ◽  
Author(s):  
Karuppiah Krishnaveni ◽  
Sepperumal Murugesan ◽  
Ayyanar Siva

A new type of selective and sensitive naphthyl hydrazone anchored Schiff base derivative (PYNA) was synthesized and applied to the fluorogenic and chromogenic recognition of both tryptamine (TryptA) and F−ions, further it has good cell permeability and biocompatibility in zebrafish embryos and HeLa cells.


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