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Mária Péter

Publications and source records attributed to Mária Péter.

11 recordsLinked to original sources
PubMed2006

Attachment of streptavidin to beta-cyclodextrin molecular printboards via orthogonal host-guest and protein-ligand interactions.

Streptavidin (SAv) is attached to beta-cyclodextrin (beta-CD) self-assembled monolayers (SAMs) via orthogonal host-guest and SAv-biotin interactions. The orthogonal linkers consist of a biotin functionality for binding to SAv and adamantyl functionalities for host-guest interactions at beta-CD SAMs. SAv complexed to excess monovalent linker in solution and then attached to a beta-CD SAM could be removed by rinsing with a 10 mM beta-CD solution. When SAv was attached to the beta-CD SAM via the divalent linker, it was impossible to remove SAv from the surface by the same rinsing procedure. This is interpreted by assuming that two SAv binding pockets are oriented towards the beta-CD SAM resulting in (labile) divalent and (stable) tetravalent beta-CD-adamantyl interactions for the mono- and divalent linkers, respectively. This was confirmed by experiments at varying beta-CD concentrations. When the [linker]/[SAv] ratio is reduced, a clear trend in the divalent-linker case is seen: the less linker the more protein could be removed from the surface. It is proven that the orthogonality of the binding motifs and the stability of the divalent linker at the beta-CD SAM allows the stepwise assembly of the complex at the beta-CD SAM by first adsorbing the linker, followed by SAv. This stepwise assembly allows the controlled heterofunctionalization of surface-immobilized SAv.

Adsorption↗
PubMed2005

Supramolecular microcontact printing and dip-pen nanolithography on molecular printboards.

The transfer of functional molecules onto self-assembled monolayers (SAMs) by means of soft and scanning-probe lithographic techniques-microcontact printing (muCP) and dip-pen nanolithography (DPN), respectively-and the stability of the molecular patterns during competitive rinsing conditions were examined. A series of guests with different valencies were transferred onto beta-cyclodextrin- (beta-CD-) terminated SAMs and onto reference hydroxy-terminated SAMs. Although physical contact was sufficient to generate patterns on both types of SAMs, only molecular patterns of multivalent guests transferred onto the beta-CD SAMs were stable under the rinsing conditions that caused the removal of the same guests from the reference SAMs. The formation of kinetically stable molecular patterns by supramolecular DPN with a lateral resolution of 60 nm exemplifies the use of beta-CD-terminated SAMs as molecular printboards for the selective immobilization of printboard-compatible guests on the nanometer scale through the use of specific, multivalent supramolecular interactions. Electroless deposition of copper on the printboard was shown to occur selectively on the areas patterned with dendrimer-stabilized gold nanoparticles.

Journal Article↗
PubMed2005

Electrochemistry of surface-grafted stimulus-responsive monolayers of poly(ferrocenyldimethylsilane) on gold.

Poly(ferrocenyldimethylsilane)s with various degrees of polymerization and featuring a thiol end group were chemically end-grafted onto gold substrates by self-assembly, forming redox-active monolayers. The monolayers were characterized by contact angle measurements, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. Layer thickness values were determined by surface plasmon resonance spectroscopy and ellipsometry. The electrochemical properties of these films in aqueous NaClO(4) were studied using cyclic voltammetry (CV), differential pulse voltammetry, chronoamperometry, and chronocoulometry. Cyclic voltammograms showed two reversible redox peaks, indicating a stepwise oxidation of the electroactive sites. The first oxidation step showed reversible behavior at low scan rates and quasi-reversible behavior at higher scan rates. Peak currents (i(p)) plotted against the square root of scan rates (v(1/2)) for the first oxidation peak and for the corresponding reduction peak exhibited a linear dependence, indicating that the oxidation process in the first step is controlled by the diffusion of counterions into the polymer film. For the second oxidation peak and the corresponding reduction peak, i(p) varied linearly with v. This redox behavior is characteristic of surface-immobilized electroactive layers. The higher reversibility of the second oxidation and reduction waves in the CV experiments was explained from the solvation of the surface-grafted poly(ferrocenylsilane) (PFS) chains, which depends on the degree of oxidation. Oxidized PFS films are swollen in the aqueous electrolyte solutions, leading to a higher segmental mobility of the polymer chains and a much increased counterion mobility within the film. Kinetic parameters for the redox processes were obtained from chronocoulometry experiments.

Journal Article↗
PubMed2005

Multivalent host-guest interactions between beta-cyclodextrin self-assembled monolayers and poly(isobutene-alt-maleic acid)s modified with hydrophobic guest moieties.

Poly(isobutene-alt-maleic acid)s modified with p-tert-butylphenyl or adamantyl groups interact with beta-cyclodextrin self-assembled monolayers (beta-CD SAMs) by inclusion of the hydrophobic substituents in the beta-cyclodextrin cavities. The adsorption was shown to be strong, specific, and irreversible. Even with a monovalent competitor in solution, adsorption to the beta-CD SAMs was observed, and desorption proved impossible. The adsorbed polymer layer was very thin as evidenced by surface plasmon resonance spectroscopy and AFM. Apparently, all or most hydrophobic groups of the polymers were employed efficiently in multivalent binding, as was further supported by the absence of specific binding of beta-CD-modified gold nanoparticles to the polymer surface assemblies. Supramolecular microcontact printing of the polymers onto the beta-CD SAMs led to assembly formation in the targeted areas of the substrates.

Alkenes↗
PubMed2005

Comparison of column performances in direct high-performance liquid chromatographic enantioseparation of 1- or 3-methyl-substituted tetrahydroisoquinoline analogs. Application of direct and indirect methods.

The enantioseparability of 1- or 3-methyl-substituted tetrahydroisoquinolines was investigated by direct and indirect high-performance liquid chromatography. Alpha- and beta-cyclodextrin-, macrocyclic glycopeptide- and cellulose-based chiral columns and isothiocyanate- and Sanger-type chiral derivatizing agents (CDAs) were applied to attain satisfactory enantioseparation. Of the chiral columns, beta-cyclodextrin-, vancomycin- and teicoplanin-containing macrocyclic glycopeptide-based columns appeared to be most suitable; of the CDAs, (1S,2R)-1-acetoxy-1-phenyl-2-propyl isothiocyanate was most favorable. The differences between the selectivities of the columns and CDAs were compared and optimized to yield the best resolution.

Chromatography, High Pressure Liquid↗
PubMed2005

Molecular printboards on silicon oxide: lithographic patterning of cyclodextrin monolayers with multivalent, fluorescent guest molecules.

Three compounds bearing multiple adamantyl guest moieties and a fluorescent dye have been synthesized for the supramolecular patterning of beta-cyclodextrin (CD) host monolayers on silicon oxide using microcontact printing and dip-pen nanolithography. Patterns created on monolayers on glass were viewed by laser scanning confocal microscopy. Semi-quantitative analysis of the patterns showed that with microcontact printing approximately a single monolayer of guest molecules is transferred. Exposure to different rinsing procedures showed the stability of the patterns to be governed by specific supramolecular multivalent interactions. Patterns of the guest molecules created at CD monolayers were stable towards thorough rinsing with water, whereas similar patterns created on poly(ethylene glycol) (PEG) reference monolayers were instantly removed. The patterns on CD monolayers displayed long-term stability when stored under N(2), whereas patterns at PEG monolayers faded within a few weeks due to the diffusion of fluorescent molecules across the surface. Assemblies at CD monolayers could be mostly removed by rinsing with a concentrated CD solution, demonstrating the reversibility of the methodology. Patterns consisting of different guest molecules were produced by microcontact printing of one guest molecule and specific adsorption of a second guest molecule from solution to non-contacted areas, giving well-defined alternating assemblies. Fluorescent features of sub-micrometer dimensions were written using supramolecular dip-pen nanolithography.

Acrylonitrile↗
PubMed2004

Directed self-assembly of functionalized silica nanoparticles on molecular printboards through multivalent supramolecular interactions.

Silica nanoparticles functionalized with beta-cyclodextrin (CD) host molecules (5) have been prepared by reacting carboxylic active ester-terminated silica nanoparticles (4) with CD heptamine. Silica nanoparticles functionalized with glucosamine (6), having similar surface properties as 5 but lacking the host-guest recognition motif, were used to perform blank experiments. The CD-functionalized silica nanoparticles 5 were determined by TEM to be 55 +/- 6 nm in size. They exhibited pH-dependent aggregation, which is explained by the presence of free amino and carboxylic acid groups on the particle surface, which was corroborated by zeta potential measurements. The functionalization with CD was further confirmed by host-guest studies in solution and at CD-functionalized silicon substrates. The addition of an adamantyl-terminated dendrimer, capable of multivalent host-guest binding with CD, led to strong aggregation of the CD particles 5, but not of the glucosamine-functionalized 6. Furthermore, 5 gave strong adsorption to CD monolayers on silicon onto which adamantyl-terminated dendrimers were adsorbed, whereas 6 did not. The good discrimination between dendrimer-covered and uncovered areas of the CD monolayer substrates allowed the directed self-assembly of the silica particles 5 onto dendrimer-patterned areas created by microcontact printing.

Glucosamine↗
PubMed2004

Catalytic probe lithography: catalyst-functionalized scanning probes as nanopens for nanofabrication on self-assembled monolayers.

This article describes the use of scanning catalytic probe lithography for nanofabrication of patterns on self-assembled monolayers (SAMs) of reactive adsorbates. Catalytic writing was carried out by scanning over bis(omega-tert-butyldimethyl-siloxyundecyl)disulfide SAMs using 2-mercapto-5-benzimidazole sulfonic acid-functionalized gold-coated AFM tips. The acidic tips induced local hydrolysis of the silyl ether moieties in the contacted areas, and thus patterned surfaces were created. Diffusion effects arising from the use of an ink were excluded in these type of experiments, and therefore structures with well-defined shapes and sizes were produced. The smallest lines drawn by this technique were about 25 nm wide, corresponding to the actual contact area of the tip. Lateral force microscopy studies performed on different SAMs helped to clarify the nature and cause of the friction contrasts observed by AFM. Dendritic wedges with thiol functions inserted into the catalytically written areas, thus enhancing the height contrast. The created patterns open possibilities to build 3D nanostructures.

Journal Article↗
PubMed2004

Electrochemically induced morphology and volume changes in surface-grafted poly(ferrocenyldimethylsilane) monolayers.

Poly(ferrocenyldimethylsilanes), composed of alternating ferrocene and dimethylsilane units in their main chain and featuring a thiol end group, were self-assembled to redox-active monolayers on gold. Electrochemical atomic force microscopy was employed to study the morphology of the monolayers as a function of the applied potential in situ. Surface plasmon resonance spectroscopy and spectroscopic ellipsometry measurements, performed under electrochemical control, indicated thickness changes of up to 15% upon oxidizing and reducing the surface-grafted polymers. X-ray reflectivity measurements unambiguously showed a thickness increase upon electrochemical oxidation of the monolayers. The reversible thickness change was attributed to stretching of the polymer chains upon oxidation due to an increase in charge density and to the attraction of counterions and associated solvent molecules, which are released when the polymer film is reduced to its neutral state.

Journal Article↗
PubMed2002

[Chemical discrimination of compounds possessing an amino group].

Cyclic 1,3-amino alcohols have been successfully resolved via lipase-catalysed O-acylation of their Z derivatives, using vinyl butyrate as acyl donor in different ether solvents. A direct HPLC method was developed for the monitoring of the resolutions. Most of the screened lipases preferred the S enantiomer. Both alcohol and ester enantiomers were obtained in ee > 90% after gram-scale resolutions. A new isothiocyanato-type CDA, (1S,2S)- or (1R,2R)-1,3-diacetoxy-1-(4-nitrophenyl)-2-propyl isothiocyanate [(R,R)- or (S,S)-DANI], was designed for the indirect HPLC enantioseparation of primary and secondary amino compounds. The new reagent can be readily synthetized in optically pure form (> or = 99.5%) after a straightforward two-step synthesis. It is stable chemically and stereochemically both in the solid and in the solution phase. It is available in both enantiomeric forms, allowing the appropriate selection of the elution sequence. The kinetics of derivatization was studied in detail for alpha-amino acids and for beta-blockers. The quantitativeness of reactions was ensured by optimization of reaction conditions (pH, reagent excess, temperature). As concerns the HPLC analyses of the thiourea derivatives formed, significant differences were found between selectivities of the organic modifiers applied; in most cases, MeOH proved much more effective than MeCN with respect to both retention times and resolutions. In conclusion, the new CDA was capable of the resolution of most of the investigated analytes.

Adrenergic beta-Antagonists↗