scholarly journals A Cell-penetrating Helical Polymer For siRNA Delivery to Mammalian Cells

2012 ◽  
Vol 20 (8) ◽  
pp. 1599-1609 ◽  
Author(s):  
Nathan P Gabrielson ◽  
Hua Lu ◽  
Lichen Yin ◽  
Kyung Hoon Kim ◽  
Jianjun Cheng
2021 ◽  
Author(s):  
Yu Ando ◽  
Hikaru Nakazawa ◽  
Daisuke Miura ◽  
Mitsuo Umetsu

Abstract A fusion protein comprising an antibody and a cell-penetrating peptide is a candidate molecule capable of efficient and cell-specific delivery of siRNA into cells in order to reduce the side effects of nucleic acid drugs. However, their expression in bacterial hosts, required for their development, often fails, impeding research progress. In this study, we separately prepared anti-EGFR nanobodies with the K-tag sequence MRHKGS at the C-terminus and arginine-9 (R9) with the Q-tag sequence LLQGS at the N-terminus, and enzymatically ligated them in vitro by microbial transglutaminase to generate Nanobody-R9, which is not expressed as a fused protein in E. coli. Nanobody-R9 exhibited a maximum reaction efficiency of 85.1%, without changing the properties of the nanobody or R9. Nanobody-R9 successfully delivered siRNA into the cells, and the cellular influx of siRNA increased with increase in the ratio of Nanobody-R9 to siRNA. We further demonstrated that the Nanobody-R9–siRNA complex, at a 30:1 ratio, induced RNAi of target mRNA with approximately 52% efficiency compared to lipofectamine.


2009 ◽  
Vol 17 (1) ◽  
pp. 95-103 ◽  
Author(s):  
Laurence Crombez ◽  
Gudrun Aldrian-Herrada ◽  
Karidia Konate ◽  
Quan N Nguyen ◽  
Gary K McMaster ◽  
...  

2017 ◽  
Vol 8 (3) ◽  
pp. 2107-2114 ◽  
Author(s):  
Siheng Li ◽  
Lin Wang ◽  
Fei Yu ◽  
Zhiling Zhu ◽  
Dema Shobaki ◽  
...  

A copper-catalyzed click reaction inside living mammalian cells is demonstrated with the use of a cell-penetrating peptide-tethered CuI ligand.


2014 ◽  
Vol 5 (7) ◽  
pp. 809-814 ◽  
Author(s):  
Anna Leonidova ◽  
Vanessa Pierroz ◽  
Luke A. Adams ◽  
Nicholas Barlow ◽  
Stefano Ferrari ◽  
...  
Keyword(s):  

Theranostics ◽  
2018 ◽  
Vol 8 (2) ◽  
pp. 549-562 ◽  
Author(s):  
Jun-Fang Zhang ◽  
Hua-Long Xiong ◽  
Jia-Li Cao ◽  
Shao-Juan Wang ◽  
Xue-Ran Guo ◽  
...  

2006 ◽  
Vol 34 (3) ◽  
pp. 335-339 ◽  
Author(s):  
F.R. Maxfield ◽  
M. Mondal

The pathways involved in the intracellular transport and distribution of lipids in general, and sterols in particular, are poorly understood. Cholesterol plays a major role in modulating membrane bilayer structure and important cellular functions, including signal transduction and membrane trafficking. Both the overall cholesterol content of a cell, as well as its distribution in specific organellar membranes are stringently regulated. Several diseases, many of which are incurable at present, have been characterized as results of impaired cholesterol transport and/or storage in the cells. Despite their importance, many fundamental aspects of intracellular sterol transport and distribution are not well understood. For instance, the relative roles of vesicular and non-vesicular transport of cholesterol have not yet been fully determined, nor are the non-vesicular transport mechanisms well characterized. Similarly, whether cholesterol is asymmetrically distributed between the two leaflets of biological membranes, and if so, how this asymmetry is maintained, is poorly understood. In this review, we present a summary of the current understanding of these aspects of intracellular trafficking and distribution of lipids, and more specifically, of sterols.


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