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Demirel G.,Gazi University | Demirel G.,Biyomedtek Center for Bioengineering | Buyukserin F.,TOBB University of Economics and Technology
Langmuir | Year: 2011

There is an increasing interest for the utilization of biomolecules for fabricating novel nanostructures due to their ability for specific molecular recognition, biocompatibility, and ease of availability. Among these molecules, diphenylalanine (Phe-Phe) dipeptide is considered as one of the simplest molecules that can generate a family of self-assembly based nanostructures. The properties of the substrate surface, on which the self-assembly process of these peptides occurs, play a critical role. Herein, we demonstrated the influence of surface texture and functionality on the self-assembly of Phe-Phe dipeptides using smooth silicon surfaces, anodized aluminum oxide (AAO) membranes, and poly(chloro-p-xylylene) (PPX) films having columnar and helical morphologies. We found that helical PPX films, AAO, and silicon surfaces induce similar self-assembly processes and the surface hydrophobicity has a direct influence for the final dipeptide structure whether being in an aggregated tubular form or creating a thin film that covers the substrate surface. Moreover, the dye staining data indicates that the surface charge properties and hence the mechanism of the self-assembly process are different for tubular structures as opposed to the peptidic film. We believe that our results may contribute to the control of surface-induced self-assembly of peptide molecules and this control can potentially allow the fabrication of novel peptide based materials with desired morphologies and unique functionalities for different technological applications. © 2011 American Chemical Society. Source


Demirel G.,Gazi University | Demirel G.,Biyomedtek Center for Bioengineering | Tamer U.,Gazi University
Nanotechnology | Year: 2012

We demonstrated the fabrication and application of well-ordered and vertically aligned dipeptide nanostructures based on a simple gas phase deposition. Deposited nanostructures exhibited the superhydrophobic property with a very low sliding angle. Highly reproducible SERS data have also been obtained after combining deposited films with a thin layer of gold. In addition to these, directional peptide films were, for the first time, successfully fabricated based on the oblique angle deposition technique. We believe that such bio-inspired materials would have a great impact in several technological applications involving catalysis, tissue engineering and biosensors. © 2012 IOP Publishing Ltd. Source


Erdogan H.,Gazi University | Sakalak H.,Selcuk University | Yavuz M.S.,Selcuk University | Demirel G.,Gazi University | Demirel G.,Biyomedtek Center for Bioengineering
Langmuir | Year: 2013

Further understanding of the interactions between nanoparticles (NPs) and biological molecules offers new possibilities in the applications of nanomedicine and nanodiagnostics. The properties of NPs, including size, shape, and surface functionality, play a decisive role in these interactions. Herein, we evaluated the influences of gold NPs (AuNPs) with different sizes (5-60 nm) and shapes (i.e., spherical, rod, and cage) on the self-assembly of diphenylalanine (Phe-Phe) dipeptides. We found that the size of AuNPs smaller than 10 nm did not affect the self-assembly process of Phe-Phe, while bigger AuNPs (>10 nm) caused the formation of starlike peptide morphologies connected to one center. In the case of shape differences, nanorod and nanocage morphologies acted differently than spherical ones and caused the formation of densely packed, networklike dipeptide morphologies. In addition to these experiments, by combining photothermal properties of AuNPs with a Phe-Phe-based organogel having a thermo-responsive property, we demonstrated that the degelation process of AuNPs embedded organogels may be controlled by laser illumination. Complete degelation was achieved in about 10 min. We believe that such control may open the door to new opportunities for a number of applications, such as controlled release of drugs and tissue engineering. © 2013 American Chemical Society. Source


Sahin F.,Gazi University | Turan E.,Gazi University | Tumturk H.,Gazi University | Demirel G.,Gazi University | Demirel G.,Biyomedtek Center for Bioengineering
Analyst | Year: 2012

Core-shell magnetic nanoparticles (MNPs) offer tremendous opportunities in a large range of applications in biomedicine due to their superior magnetic properties, biocompatibility and suitability for modification. In most cases, these characteristic features are determined by their shell chemistry and morphology. Herein, we demonstrate a comparative study of silica and polydopamine (PDOP) coating onto MNP surfaces based on synthesis, characterization and usage in a bio-separation platform. It was found that monodispersed MNPs may be easily obtained on silica coating of varying shell thickness, whereas a continuous PDOP layer observed around the MNPs prevents the formation of the dispersed form. On the other hand, PDOP coated MNPs exhibited better superparamagnetic behavior and biological modification ability compared to the silica coated form. © 2012 The Royal Society of Chemistry. Source


Demirel G.B.,Gazi University | Buyukserin F.,TOBB University of Economics and Technology | Morris M.A.,Trinity College Dublin | Morris M.A.,University College Cork | And 2 more authors.
ACS Applied Materials and Interfaces | Year: 2012

One-dimensional nanoporous polymeric nanofibers have been fabricated within an anodic aluminum oxide (AAO) membrane by a facile approach based on selective etching of poly(dimethylsiloxane) (PDMS) domains in polystyrene-block- poly(dimethylsiloxane) (PS-b-PDMS) block copolymers that had been formed within the AAO template. It was observed that prior to etching, the well-ordered PS-b-PDMS nanofibers are solid and do not have any porosity. The postetched PS nanofibers, on the other hand, had a highly porous structure having about 20-50 nm pore size. The nanoporous polymeric fibers were also employed as a drug carrier for the native, continuous, and pulsatile drug release using Rhodamine B (RB) as a model drug. These studies showed that enhanced drug release and tunable drug dosage can be achieved by using ultrasound irradiation. © 2011 American Chemical Society. Source

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