| Literature DB >> 25302483 |
Markus Schomaker1, Doreen Killian2, Saskia Willenbrock3, Dag Heinemann4, Stefan Kalies4, Anaclet Ngezahayo5, Ingo Nolte3, Tammo Ripken4, Christian Junghanß2, Heiko Meyer4,6, Hugo Murua Escobar2,3, Alexander Heisterkamp4,7.
Abstract
Gold nanoparticle mediated (GNOME) laser transfection is a powerful technique to deliver small biologically relevant molecules into cells. However, the transfection of larger and especially negatively charged DNA remains challenging. The efficiency for pDNA was 0.57% using parameter that does not influence the endo- and exogenous DNA. In order to gain a deeper understanding of the actual molecule uptake process, the uptake efficiency was determined using molecules of different sizes. It was evaluated that uncharged dextran molecules (2000 kDa) were delivered with an efficiency of 68%. The intracellular distribution of injected molecules was visualized and larger molecules were primary found in the cytoplasm. Patch clamp measurements suggested a permeabilization time up to 15 minutes. The uptake efficiency depended on the size and charge of the molecule to deliver as well as the cell size. A minor role for transfection plays the cell type since primary stem cells were successfully transfected. The perforation efficiency of semi-adherent and suspension cells is influenced by the cell and molecule size.Entities:
Keywords: DNA; GNOME laser transfection; gold nanoparticles; molecule size; stem cells
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Year: 2014 PMID: 25302483 DOI: 10.1002/jbio.201400065
Source DB: PubMed Journal: J Biophotonics ISSN: 1864-063X Impact factor: 3.207