Quantitative assessment of cellular uptake and cytosolic access of antibody in living cells by an enhanced split GFP complementation assay

2015 ◽  
Vol 467 (4) ◽  
pp. 771-777 ◽  
Author(s):  
Ji-sun Kim ◽  
Dong-Ki Choi ◽  
Seong-wook Park ◽  
Seung-Min Shin ◽  
Jeomil Bae ◽  
...  
2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Nadia Milech ◽  
Brooke AC Longville ◽  
Paula T Cunningham ◽  
Marie N Scobie ◽  
Heique M Bogdawa ◽  
...  

2013 ◽  
Vol 41 (15) ◽  
pp. e152-e152 ◽  
Author(s):  
Xuemei Zhang ◽  
Yang Song ◽  
Akash Y. Shah ◽  
Virzhiniya Lekova ◽  
Arjun Raj ◽  
...  

2016 ◽  
Vol 40 (4) ◽  
pp. 3252-3260 ◽  
Author(s):  
Nan Xie ◽  
Ke Feng ◽  
Bin Chen ◽  
Chen-Ho Tung ◽  
Li-Zhu Wu

Two-photon imaging polynorbornenes were fabricated directly from photochromic spiropyran, RGD peptides and hydrophilic PEG monomers via modular ROMP.


2019 ◽  
Vol 74 (1) ◽  
pp. 63-71 ◽  
Author(s):  
Sylvain Clède ◽  
Christophe Sandt ◽  
Paul Dumas ◽  
Clotilde Policar

Presented here is the exploitation of synchrotron infrared spectromicroscopy to evaluate the feasibility of monitoring the cellular uptake of rhenium-tris-carbonyl-tagged (Re(CO)3) lipophilic chains in living cells. To this aim, an in-house thermostated microfluidic device was used to limit water absorption while keeping cells alive. Indeed, cells showed a high survival rate in the microfluidic device over the course of the experiment, proving the short-term biocompatibility of the device. We recorded spectra of single, living, fully hydrated breast cancer MDA-MB231 cells and could follow the penetration of the rhenium complexes for up to 2 h. Despite the strong variations observed in the uptake kinetics between individual cells, the Re(CO)3 complex was traced inside the cells at low concentration and shown to enter them on the hour time scale by active transport.


2010 ◽  
Vol 24 (3-4) ◽  
pp. 303-307 ◽  
Author(s):  
Petr Praus ◽  
Eva Kocišová ◽  
Peter Mojzeš ◽  
Josef Štepánek ◽  
Franck Sureau ◽  
...  

Time-resolved confocal microspectrofluorometry and fluorescence microimaging were used to monitor how the model antisense oligonucleotide is transported into 3T3 living cells and distributed inside them. Phosphorothioate analog of 15-mer oligothymidylate labeled by ATTO 425 was complexed with Zn(II) 5,10,15,20-tetrakis(4-N-methylpyridyl) porphyrin as an uptake-mediating agent. Homodyne phase-resolved technique based on a high frequency analog modulation of both exciting diode laser and detector image intensifier was used for time-resolved measurements. Decay-time data obtained within a broad range spectral region have provided unique information about the fate of both fluorophores inside the cell.


2017 ◽  
Vol 35 (2) ◽  
pp. 1700331 ◽  
Author(s):  
Siwen Li ◽  
Caiping Tian ◽  
Yuxi Liu ◽  
Zhaohui Wang ◽  
Yi Ma ◽  
...  
Keyword(s):  

2014 ◽  
Vol 5 (10) ◽  
pp. 3995 ◽  
Author(s):  
Alberto A. R. Mota ◽  
Pedro H. P. R. Carvalho ◽  
Bruna C. Guido ◽  
Heibbe C. B. de Oliveira ◽  
Thereza A. Soares ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document