0000000000210351

AUTHOR

Christof M. Niemeyer

0000-0002-8837-081x

showing 15 related works from this author

Label-Free Pyrophosphate Recognition with Functionalized Asymmetric Nanopores

2016

[EN] The label¿free detection of pyrophosphate (PPi) anions with a nanofluidic sensing device based on asymmetric nanopores is demonstrated. The pore surface is functionalized with zinc complexes based on two di(2¿picolyl)amine [bis(DPA)] moieties using carbodiimide coupling chemistry. The complexation of zinc (Zn2+) ion is achieved by exposing the modified pore to a solution of zinc chloride to form bis(Zn2+¿DPA) complexes. The chemical functionalization is demonstrated by recording the changes in the observed current¿voltage (I¿V) curves before and after pore modification. The bis(Zn2+¿DPA) complexes on the pore walls serve as recognition sites for pyrophosphate anion. The experimental re…

Adenosine monophosphatechemistry.chemical_elementNanotechnology02 engineering and technologyZincPicolinic acid010402 general chemistry01 natural sciencesPyrophosphateBiomaterialsNanoporeschemistry.chemical_compoundPolymer chemistryGeneral Materials ScienceAminesPicolinic AcidsStaining and LabelingGeneral Chemistry021001 nanoscience & nanotechnologyPhosphate0104 chemical sciencesDiphosphatesAdenosine diphosphatechemistryFISICA APLICADASurface modificationAmine gas treating0210 nano-technologyBiotechnologySmall
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Configurable low-cost plotter device for fabrication of multi-color sub-cellular scale microarrays.

2014

We report on the construction and operation of a low-cost plotter for fabrication of microarrays for multiplexed single-cell analyses. The printing head consists of polymeric pyramidal pens mounted on a rotation stage installed on an aluminium frame. This construction enables printing of microarrays onto glass substrates mounted on a tilt stage, controlled by a Lab-View operated user interface. The plotter can be assembled by typical academic workshops from components of less than 15 000 Euro. The functionality of the instrument is demonstrated by printing DNA microarrays on the area of 0.5 squared centimeters using up to three different oligonucleotides. Typical feature sizes are 5 μm diam…

FabricationMaterials scienceScale (ratio)NanotechnologyMultiplexingBiomaterialsUser-Computer InterfacePlotterHumansGeneral Materials ScienceBiochipOligonucleotide Array Sequence AnalysisEGF ReceptorsEpidermal Growth FactorOligonucleotideDNA-directed protein immobilization EGF receptors device automation multiplexed patterns polymer pen lithographyGeneral ChemistryMicrofluidic Analytical TechniquesErbB ReceptorsTissue Array AnalysisCosts and Cost AnalysisMCF-7 CellsPrintingDNA microarraySingle-Cell AnalysisBiotechnologySmall (Weinheim an der Bergstrasse, Germany)
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A Protein-Interaction Array Inside a Living Cell

2013

Cell phenotype is determined by protein network states that are maintained by the dynamics of multiple protein interactions.1 Fluorescence microscopy approaches that measure protein interactions in individual cells, such as by Forster resonant energy transfer (FRET), are limited by the spectral separation of fluorophores and thus are most suitable to analyze a single protein interaction in a given cell. However, analysis of correlations between multiple protein interactions is required to uncover the interdependence of protein reactions in dynamic signal networks. Available protein-array technologies enable the parallel analysis of interacting proteins from cell extracts, however, they can …

ImmunoprecipitationRecombinant Fusion Proteinsprotein-protein interactionsImmobilized Nucleic AcidsProtein Array AnalysisreceptorsDNA Single-StrandedCatalysisProtein–protein interactionReceptors G-Protein-CoupledBimolecular fluorescence complementationProtein Array AnalysisChlorocebus aethiopsFluorescence microscopeFluorescence Resonance Energy TransferAnimalsProtein Interaction MapsProtein kinase Amultiplexed assayChemistryProteinsProtein-protein interactions Dip Pen Nanolithography Protein KinaseDNA directed immobilizationGeneral MedicineGeneral ChemistryCommunicationssurface-immobilizationKineticsLuminescent ProteinsFörster resonance energy transferBiochemistryMicroscopy FluorescenceCOS CellsBiophysicsSignal transductionAntibodies Immobilizedsignal transduction
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Fluoride-induced modulation of ionic transport in asymmetric nanopores functionalized with “caged” fluorescein moieties

2016

[EN] We demonstrate experimentally and theoretically a nanofluidic fluoride sensing device based on a single conical pore functionalized with "caged" fluorescein moieties. The nanopore functionalization is based on an amine-terminated fluorescein whose phenolic hydroxyl groups are protected with tert-butyldiphenylsilyl (TBDPS) moieties. The protected fluorescein (Fcn-TBDPS-NH2) molecules are then immobilized on the nanopore surface via carbodiimide coupling chemistry. Exposure to fluoride ions removes the uncharged TBDPS moieties due to the fluoride-promoted cleavage of the silicon-oxygen bond, leading to the generation of negatively charged groups on the fluorescein moieties immobilized on…

Life sciences; biologyReaction stepAnalytical chemistryHalideIonic bonding02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundNanoporechemistryddc:570FISICA APLICADASurface modificationMoleculeGeneral Materials ScienceFluorescein0210 nano-technologyFluorideNanoscale
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Cesium-Induced Ionic Conduction through a Single Nanofluidic Pore Modified with Calixcrown Moieties

2017

[EN] We demonstrate experimentally and theoretically a nanofluidic device for the selective recognition of the cesium ion by exploiting host¿guest interactions inside confined geometry. For this purpose, a host molecule, i.e., the amine-terminated p-tert-butylcalix[4]arene-crown (tBuC[4]C¿NH2), is successfully synthesized and functionalized on the surface of a single conical nanopore fabricated in a poly(ethylene terephthalate) (PET) membrane through carbodiimide coupling chemistry. On exposure to the cesium cation, the t-BuC[4]C¿Cs+ complex is formed through host¿guest interaction, leading to the generation of positive fixed charges on the pore surface. The asymmetrical distribution of the…

Materials scienceAnalytical chemistryChemical modification02 engineering and technologySurfaces and InterfacesConical surface010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsAlkali metal01 natural sciences0104 chemical sciencesIonNanoporeMembraneChemical physicsFISICA APLICADAElectrochemistryIonic conductivityMoleculeGeneral Materials Science0210 nano-technologySpectroscopy
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Tumor-Associated MUC1 Tandem-Repeat Glycopeptide Microarrays to Evaluate Serum- and Monoclonal-Antibody Specificity

2009

Repetitive Sequences Amino Acidmedicine.drug_classMolecular Sequence DataMonoclonal antibodyCatalysisMiceTandem repeatAntibody SpecificityNeoplasmsmedicineAnimalsAmino Acid SequencePeptide sequenceMUC1biologyMicroarray analysis techniquesChemistryImmune SeraMucin-1GlycopeptidesAntibodies MonoclonalGeneral MedicineGeneral ChemistryMicroarray AnalysisMolecular biologyGlycopeptideBiochemistrybiology.proteinAntibodyDNA microarrayAngewandte Chemie International Edition
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A redox-sensitive nanofluidic diode based on nicotinamide-modified asymmetric nanopores

2017

[EN] We demonstrate a redox-sensitive nanofluidic diode whose ion rectification is modulated by the oxidation and reduction of chemical moieties incorporated on its surface. To achieve this goal, we have first synthesized the chemical compounds 1-(4-aminobutyl)-3-carbamoylpyridin-1-ium (Nic-BuNH2) and 3-carbamoyl-1-(2,4-dinitrophenyl)pyridinium (Nic-DNP). Then, the surface of track-etched single asymmetric nanopores is decorated with the redox-sensitive Nic-BuNH2 and Nic-DNP molecules using carbodiimide coupling chemistry and Zincke reaction, respectively. The success of the modification reactions is monitored through the changes in the current¿voltage (I¿V) curves prior to and after pore f…

Track-etchingReducing agent02 engineering and technology010402 general chemistryPhotochemistry01 natural sciencesRedoxIonchemistry.chemical_compoundMaterials ChemistryMoleculeOrganic chemistryRedox reactionSurface chargeElectrical and Electronic EngineeringNicotinamideInstrumentationCurrent rectificationMetals and Alloys021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsNanoporechemistrySurface functionalizationFISICA APLICADASurface modificationPyridiniumSynthetic nanopores0210 nano-technologySensors and Actuators B: Chemical
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Biochips for cell biology by combined dip-pen nanolithography and DNA-directed protein immobilization.

2013

A general methodology for patterning of multiple protein ligands with lateral dimensions below those of single cells is described. It employs dip pen nanolithography (DPN) patterning of DNA oligonucleotides which are then used as capture strands for DNA-directed immobilization (DDI) of oligonucleotide-tagged proteins. This study reports the development and optimization of PEG-based liquid ink, used as carrier for the immobilization of alkylamino-labeled DNA oligomers on chemically activated glass surfaces. The resulting DNA arrays have typical spot sizes of 4-5 μm with a pitch of 12 μm micrometer. It is demonstrated that the arrays can be further functionalized with covalent DNA-streptavidi…

Materials scienceSurface PropertiesGreen Fluorescent ProteinsOligonucleotidesLigandsBiomaterialsCell membranechemistry.chemical_compoundEpidermal growth factorDip-pen nanolithographyCell Line TumorMaterials TestingMicrochip Analytical ProceduresmedicineHumansNanotechnologyGeneral Materials ScienceBiotinylationBiochipOligonucleotide Array Sequence AnalysisEpidermal Growth FactorOligonucleotideCell MembraneProteinsNanolitographyGeneral ChemistryCell BiologyDNABiochipCell biologymedicine.anatomical_structurecell.chemistryBiotinylationMCF-7 CellsGlassproteinDNABiotechnologyProtein ligandSmall (Weinheim an der Bergstrasse, Germany)
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Lithium Ion Recognition with Nanofluidic Diodes through Host-Guest Complexation in Confined Geometries

2018

[EN] The lithium ion recognition is receiving significant attention because of its application in pharmaceuticals, lubricants and, especially, in energy technology. We present a nanofluidic device for specific lithium ion recognition via host guest complexation in a confined environment. A lithium-selective receptor molecule, the aminoethyl-benzo-12-crown-4 (BC12C4-NH2), is designed and functionalized on single conical nanopores in polyethylene terephthalate (PET) membranes. The native carboxylic acid groups on the pore walls are covalently linked with the crown ether moieties and the process is monitored from the changes in the current voltage (I-V) curves. The B12-crown-4 moieties are kno…

chemistry.chemical_classificationchemistry.chemical_elementIon current02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistryAlkali metal01 natural sciencesChloride0104 chemical sciencesAnalytical ChemistryIonchemistry.chemical_compoundMembranechemistryFISICA APLICADAmedicineLithium chlorideLithium0210 nano-technologyCrown ethermedicine.drug
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Preparation of Biomolecule Microstructures and Microarrays by Thiol-ene Photoimmobilization

2009

A mild, fast and flexible method for photoimmobilization of biomolecules based on the light-initiated thiol-ene reaction has been developed. After investigation and optimization of various surface materials, surface chemistries and reaction parameters, microstructures and microarrays of biotin, oligonucleotides, peptides, and MUC1 tandem repeat glycopeptides were prepared with this photoimmobilization method. Furthermore, MUC1 tandem repeat glycopeptide microarrays were successfully used to probe antibodies in mouse serum obtained from vaccinated mice. Dimensions of biomolecule microstructures were shown to be freely controllable through photolithographic techniques, and features down to 5 …

LightUltraviolet RaysMicroarraysOligonucleotidesBiotinNanotechnologyCorrelated Electron Systems / High Field Magnet Laboratory (HFML)BiochemistryAntibodiesMicechemistry.chemical_compoundBiotinTandem repeatIR-72760AnimalsSulfhydryl CompoundsBiochipMolecular BiologyEne reactionchemistry.chemical_classificationthiol–ene reactionphotochemistryThiol-ene reactionOligonucleotideBiomoleculeMucin-1Organic ChemistryGlycopeptidesMicroarray AnalysisPhotochemical ProcessesImmobilized ProteinsBiochipschemistryimmobilizationMolecular MedicineDNA microarrayMETIS-273430ChemBioChem
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Titelbild: Tumor-Associated MUC1 Tandem-Repeat Glycopeptide Microarrays to Evaluate Serum- and Monoclonal-Antibody Specificity (Angew. Chem. 44/2009)

2009

Tandem repeatBiochemistryChemistrymedicine.drug_classmedicineGeneral MedicineDNA microarrayMonoclonal antibodyMolecular biologyGlycopeptideMUC1Angewandte Chemie
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Ionic Transport through Chemically Functionalized Hydrogen Peroxide-Sensitive Asymmetric Nanopores

2015

We describe the fabrication of a chemical-sensitive nanofluidic device based on asymmetric nanopores whose transport characteristics can be modulated upon exposure to hydrogen peroxide (H2O2). We show experimentally and theoretically that the current-voltage curves provide a suitable method to monitor the H2O2-mediated change in pore surface characteristics from the electronic readouts. We demonstrate also that the single pore characteristics can be scaled to the case of a multipore membrane whose electric outputs can be readily controlled. Because H2O2 is an agent significant for medical diagnostics, the results should be useful for sensing nanofluidic devices.

Medical diagnosticFabricationMaterials scienceSurface PropertiesIonic bondingNanotechnologyIonNernst-Planck equationsNanoporeschemistry.chemical_compoundGeneral Materials ScienceAminesHydrogen peroxideIon transporterIonsIon TransportCurrent rectificationPolyethylene TerephthalatesH2O2-sensitive porefood and beveragesHydrogen PeroxideModels TheoreticalNanoporeMembranechemistryFISICA APLICADAAsymmetric nanoporesChemical functionalizationACS Applied Materials & Interfaces
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18F-labeling of peptides by means of an organosilicon-based fluoride acceptor.

2006

Fluorine-18 is among the most commonly used radionuclides for positron emission tomography (PET). This non-invasive imaging technique is capable of providing in vivo information about the distribution of radiolabeled biomolecules by 1808 coincidence detection of two simultaneously emitted photons from positron–electron annihilation. Although a number of different radiotracers have been successfully employed in PET, only a few, such as 2-[F]fluoro-2-deoxy-d-glucose (FDG) and [F]fluorodopa, have gained widespread application in nuclear medicine. The reason for this is that the regioselective introduction of F into tracer molecules is often non-specific and radiochemical yields (RCY) of the Fl…

Fluorine RadioisotopesAqueous solutionMolecular StructureInorganic chemistrySynthonRadiochemistryRegioselectivityGeneral ChemistryPeptides CyclicCatalysisPeptide FragmentsIsotopic labelingchemistry.chemical_compoundFluorideschemistryModels ChemicalYield (chemistry)Isotope LabelingMoleculeIndicators and ReagentsOrganosilicon CompoundsAcetonitrileOrganosiliconAngewandte Chemie (International ed. in English)
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18F-Markierung von Peptiden mithilfe eines Organosilicium-Fluoridacceptors

2006

StereochemistryChemistryGeneral MedicineAngewandte Chemie
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Cover Picture: Tumor-Associated MUC1 Tandem-Repeat Glycopeptide Microarrays to Evaluate Serum- and Monoclonal-Antibody Specificity (Angew. Chem. Int.…

2009

biologyChemistrymedicine.drug_classGeneral ChemistryMonoclonal antibodyMolecular biologyCatalysisGlycopeptideSolid-phase synthesisTandem repeatbiology.proteinmedicineCover (algebra)DNA microarrayAntibodyMUC1Angewandte Chemie International Edition
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