Dimerization of a cell-penetrating peptide leads to enhanced cellular uptake and drug delivery

• Jan Hoyer,
• Ulrich Schatzschneider,
• Michaela Schulz-Siegmund and
• Ines Neundorf

Beilstein J. Org. Chem. 2012, 8, 1788–1797, doi:10.3762/bjoc.8.204

• a dramatically improved capacity to internalize into various cell lines, even primary cells, using flow cytometry and fluorescence microscopy. Cell viability assays indicated increased cytotoxicity of the dimer presumably caused by membrane leakage; however, this effect turned out to be dependent on

• investigated the intracellular distribution pattern of the fluorescently-labeled peptide in HEK-293 by fluorescence microscopy (Figure 2). The punctate uptake pattern speaks in favor of an endocytic internalization mode and is also observed for sC18, which is in line with previous reports [8]. Therefore, the

ROMP-Derived cyclooctene-based monolithic polymeric materials reinforced with inorganic nanoparticles for applications in tissue engineering

• Franziska Weichelt,
• Solvig Lenz,
• Stefanie Tiede,
• Ingrid Reinhardt,
• Bernhard Frerich and
• Michael R. Buchmeiser

Beilstein J. Org. Chem. 2010, 6, 1199–1205, doi:10.3762/bjoc.6.137

• -derived stromal cells. Each data point is the average of 12 data points. (b) Fluorescence microscopy images of living cells after one and four days of cultivation; cells (human adipose tissue-derived stem cells) grown on a COE-based scaffold reinforced with 12 wt % CaCO3. ROMP-based synthesis of cis-5

Bioorthogonal metabolic glycoengineering of human larynx carcinoma (HEp-2) cells targeting sialic acid

• Arne Homann,
• Riaz-ul Qamar,
• Sevnur Serim,
• Petra Dersch and
• Jürgen Seibel

Beilstein J. Org. Chem. 2010, 6, No. 24, doi:10.3762/bjoc.6.24

• detectable. In order to analyze the natural background fluorescence of HEp-2, one sample was incubated without any additional carbohydrates. The cells were analyzed by fluorescence microscopy (580 nm for TAMRA staining and at 525 nm for fluorescein). At either wavelength, the negative control does not show

• 2 mM CuSO4, 10 mM sodium ascorbate and 2 mM Tris-[(1-benzyl-1H-1,2,3-triazol-4-yl) methyl]amine (TBTA) in DMSO. After 1 h each well was washed several times with DMSO/water (1:1) and subsequently examined by fluorescence microscopy. Top left: HEp-2 cells incorporated with Ac4GlcNAz 16, labelled with