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Cell-penetrating peptides represent an emerging class of carriers capable of effective cellular delivery. This work demonstrates the preparation and investigation of efficient CPPs. We have already shown that the presence of 4-((4-(dimethylamino)phenyl)azo)benzoic acid (Dabcyl) and Trp greatly increase the uptake of oligoarginines. This work is a further step in that direction. We have explored the possibility of employing unnatural, aromatic amino acids, to mimic Trp properties and effects. The added residues allow the introduction of aromaticity, not as a side-chain group, but rather as a part of the sequence. The constructs presented exceptional internalization on various cell lines, with an evident structure-activity relationship. The CPPs were investigated for their entry mechanisms, and our peptides exploit favorable pathways, yet one of the peptides relies highly on direct penetration. Confocal microscopy studies have shown selectivity towards the cell lines, by showing diffuse uptake in FADU cells, while vesicular uptake takes place in SCC-25 cell line. These highly active CPPs have proved their applicability in cargo delivery by successfully delivering antitumor drugs into MCF-7 and MDA-MB-231 cells. The modifications in the sequences allow the preparation of short yet highly effective constructs able to rival the penetration of well-known CPPs such as octaarginine (Arg8).

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BACKGROUND AND PURPOSE: Cell penetrating peptides are promising tools for delivery of cargo into cells, but factors limiting or facilitating their cellular uptake are largely unknown. We set out to study the effect of the biophysical properties of the cell membrane on the uptake of penetratin, a cell penetrating peptide. EXPERIMENTAL APPROACH: Using labelling with pH-insensitive and pH-sensitive dyes, the kinetics of cellular uptake and endo-lysosomal escape of penetratin were studied by flow cytometry. KEY RESULTS: We report that escape of penetratin from acidic endo-lysosomal compartments is retarded compared with its total cellular uptake. The membrane dipole potential, known to alter transmembrane transport of charged molecules, is shown to be negatively correlated with the concentration of penetratin in the cytoplasmic compartment. Treatment of cells with therapeutically relevant concentrations of atorvastatin, an inhibitor of HMG-CoA reductase and cholesterol synthesis, significantly increased endosomal escape of penetratin in two different cell types. This effect of atorvastatin correlated with its ability to decrease the membrane dipole potential. CONCLUSION AND IMPLICATIONS: These results highlight the importance of the dipole potential in regulating cellular uptake of cell penetrating peptides and suggest a clinically relevant way of boosting this process.

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There are numerous wetland rehabilitation projects worldwide, but their efficiency is seldom assessed comprehensively. Oxbow lakes are wetlands of particular sensitivity. Within a large-scale floodplain rehabilitation project in Hungary, the Old Drava Programme, water replenishment was first carried out for the Cún-Szaporca oxbow lakes, a key area in the project. To assess its sustainability, the entire hydrological system has been monitored. From the data of hydrological monitoring (infiltration, soil moisture, groundwater/lakewater interaction) it is claimed that water replenishment involves significant losses through seepage (4.1 and 1.46 mm d-1) and evaporation (3.01 and 1.44 mm d-1) in the studied pre-intervention and replenishment periods, resp. Infiltration alone is insufficient to replenish groundwater and raise oxbow lake levels. In the critical summer half-year evaporation is intensive in the neighbouring agricultural fields. Groundwater table dynamics are controlled by hyporheic and groundwater flow. Major impact on the water balance of the oxbow lakes is exerted by the regime of the Drava River. A deepened lakebed is recommended to ensure more effective water retention in the oxbow lake. From the local study conclusions are drawn for the feasibility of rehabilitation at floodplain scale and in areas with similar hydromorphological conditions.

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Neonatal studies suggest elevated arousal can negatively influence perceptual and cognitive processes during early development. The authors explored this issue during the prenatal period by pharmacologically elevating physiological arousal in bobwhite quail (Colinus virginianus) embryos during exposure to a maternal call, then assessing preference for the familiar call following hatching. Embryos receiving norepinephrine showed a prenatal elevation in heart rate and failed to demonstrate a preference for the familiar call following hatching. Embryos not receiving norepinephrine showed no elevation in heart rate and demonstrated a preference for the familiar call. These results indicate elevated arousal can interfere with perceptual learning during the prenatal period and provide additional evidence for an optimal window of arousal necessary to foster species-typical perceptual functioning during early development.

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